Levels of certain tumor markers as differential factors between bilharzial and non-biharzial bladder cancer among Egyptian patients
© Metwally et al; licensee BioMed Central Ltd. 2011
Received: 26 January 2011
Accepted: 7 April 2011
Published: 7 April 2011
Bladder cancer is the commonest type of malignant tumors as a result of schistosomaisis which is a major healthy problem in many subtropical developing countries. The aim of this study is to comparatively elucidate the underlying biochemical tumor markers in schistosomal bladder cancer versus non-schistosomal bladder cancer when compared to normal healthy ones.
This work was performed on tissue specimens from total 25 patients and serum samples from total 30 patients versus ten healthy individuals served as control. The investigated parameters in serum are: xanthine oxidase (XO), fructosamine, lactate dehydrogense (LDH), aspartate aminotransferase (AST), alanine aminotransferase (ALT), total proteins, essential and non- essential amino acids profile, hydroxyproline, total immunoglobulin E (IgE) and tumor necrosis factor alpha (TNF-α). In addition, the current investigation also extended to study some markers in tumor bladder tissues including, pyruvate kinase enzyme (PK), lactate dehydrogenase (LDH), aspartate aminotransferase (AST) and alanine aminotransferase (ALT).
Results showed that biharzial bladder cancer patients recored more significant elevation in serum XO, fructosamine, LDH, AST, ALT, hydroxyproline, IgE and TNF-α than in bladder cancer patients when compared to control ones. While, in tissues there were significant increase in PK, LDH, AST & ALT activities of schistosomal bladder cancer than in bladder cancer as compared to control healthy patients.
It could be concluded that, bilharzial and non-bilharzial bladder cancer showed distinct biochemical profile of tumor development and progression which can be taken into consideration in diagnosis of bladder cancer.
Bladder cancer is the second most common malignancy of the genitourinary system in males and females [1, 2], accounting for 6% to 8% of all male malignancies and 2% to 3% of all female malignancies . In Africa, squamous cell carcinoma of the bladder is greatly overrepresented among the fellaheen (peasant farmers) of Egypt and the Africans of Mozambique, Zimbabwe, and Zambia (formerly Rhodesia), all countries where Schistosoma haematobium is endemic. An age-standardized mortality rate for bladder cancer of 10.8 per 100,000 males places Egypt at the top of the list of the 54 countries providing data for the 1987 WHO database .
The most common type diagnosed in North and South America, Europe and Asia is transitional cell carcinoma, which is mainly non-schistosomal bladder tumors, followed by squamous cell carcinoma which is found more in geographical regions where schistosomiasis is prevalent . One of the conditions leads to bladder cancer in Africa, the Middle East and Asia is schistosomiasis . Schistosoma haematobium is the most predominant species in the Middle East, Asia, and Africa, and the most implicated in the schistosomal bladder tumors in these regions .
No prospective study measuring the risk of developing bladder cancer in infected and uninfected persons is yet available. Although differences in relative frequencies may reflect differences in risk, the interplay of other factors, such as geopolitical variations in case finding, can result in spurious differences and erroneous associations. If the postulated association is correct, one of several conditions must obtain: the worm (1) produces a carcinogen, (2) carries a virus, or (3) is cocarcinogenic to some other insult. In this case, there are many unanswered questions regarding geographic differences in vesical cancer observed where schistosomiasis is endemic. These range from whether there is geographic uniformity in the host's reaction to infection to whether other environmental variables (such as the bright food coloring used in the candy popular in the Nile delta) interact and are additionally responsible for vesical neoplasia .
There is some evidence suggesting that oxidative stress and bladder cancer are closely related [8, 9]. Inherent oxidative stress may affect several functions in cancer cells or tumor tissue such as cell proliferation, promotion of mutations and genetic instability, alterations in cellular sensitivity to anticancer agents, invasion, and metastasis . Hydroxyl radicals, peroxides and superoxides are reactive oxygen species (ROS) that are generated during everyday metabolic processes in a normal cell. ROS generated either endogenously (mitochondria, metabolic process, inflammation etc.) or from external sources play a vital role in regulating several biologic phenomena . While increased ROS generation has traditionally been associated with tissue injury or damage of many different biomolecules including DNA, proteins, lipids and carbohydrates which are general manifestations of pathological conditions associated with infection, aging, mitochondrial DNA mutations and cellular proliferation [12–14]. Thus, excessive production of ROS or inadequacy in a normal cell's anti-oxidant defense system (or both) can cause the cell to experience oxidative stress and the increased ROS may play a broader role in cellular process associated with initiation and development of cancers . In view of the above information, the objective of this study was undertaken to investigate some key findings relevant to ROS stress in bilharzial and non bilharzial bladder cancer compared to control healthy patients. The investigated parameters in serum including xanthine oxidase (XO) enzyme activity (as a marker of purine metabolism), fructosamine (as a marker of abnormal glucose metabolism), lactate dehydrogenase (as a maker of glucose metabolism), hydroxylproline (as a maker of liver fibrosis), as well as total serum immunoglobulin E (IgE), tumor necrosis factor-alpha (TNF-α) and liver function enzymes including aspartate and alanine aminotransferase (AST & ALT), total proteins and free amino acids were also measured in serum. The study was extended to investigate some biochemical parameters in tumor tissues isolated from bladder carcinoma patients including, pyruvate kinase (PK), AST, ALT and LDH enzymes.
2. Materials and methods
2.1 Clinical cases
All cases (55 individuals) were of Egyptian bladder carcinoma patients, attending to out clinic, Medicine Oncology and Pathology Departments - National Cancer Institute - Cairo University.
Having malignant carcinoma patients.
Having bilharzial bladder lesions.
Diagnoses were confirmed by microscopic studies, where the bladder cancer was sequamous cell carcinoma (SCC).
The tumors isolated surgically from a total of 25 individuals and divided into: 1) first group consists of 12 patients with bladder carcinoma [11 male, their ages ranged from 16-58 years and 1 female has 32 years old]. 2) Second group consists of 13 subjects having schistosomale infection [9 males, their ages ranged from 21-68 and 4 females, ranged from 34-59 years old].
The serum analysis was conducted on 30 patients, 15 bladder carcinoma [10 males (17-61 years old) and 5 females (26-39 years old] and 15 bilharzial bladder carcinoma [12 males (20-63 years old) and 3 females (18-35 years old)].
2.2. Control group
serum: ten healthy individuals were served as controls to all investigated serum groups.
tissue samples: The activities were measured in nighboring mucosa (unaffected tissues) to carcinoma tissues together with bilharzias bladder carcinoma tissues.
2.3. Gross Pathology
Tissue samples of bladder carcinoma, were subjected to both pathological and histological examinations in order to evaluate the criteria of diagnosis and diseases progress, at pathology department, NCI. The original cell microscopic slid were examined and the tumors were classified as squamous carcinoma which included grade I × II and adenocarcinoma cells including grade three (III).
2.4. Parameters Assays
For Serum tests
Serum was separated by centrifugation at 3000 rpm and subjected to the following biochemical tests: XO activity was determined by the reduction of nitro-blue tetrazolium (NBT) in the presence of xanthine, forming formazan. The enzyme activity was calculated using the extinction coefficient of reduced NBT(7.5 cm2/μmol at 540 nm) . Fructosamine was determined according to the method of Parlin et al.,  where fructosamine reduces NBT under alkaline condition and forms a purple-colored formazan with an absorption maximum at 530 nm. LDH was detected in serum using Beckman LDH kit. ASTand ALT were estimated using Stanbio kit produced by Stanbio Labs, Texas, USA. A total protein was determined by using the method of Lowry et al. . Hydroxyproline content was measured using the method of Jamall et al. . The level of total IgE was measured by ELISA at 450 nm and compared with known mouse IgE standard (BD PharMingen). TNF-α was quantified using a commercial ELISA kit (Endogen, Woburn, MA). The amino acids constituents of patient serum were determined using HPLC.Eppdrof -Germany-Lc3000 amino acid analyzer.
2.5. For tumors tissues
The tissues were free of necrotic debris, connective tissues and were immediately frozen after surgrey. Measurement of ASTand ALT activities in tumors tissue homogenates were carried out by colorimetric technique of Nabih et al. . While LDH activity was assayed in the same homogenate by the method of Caboud and Wroblewski . Pyruvate kinase was determined by using the method of Ibsen et al. .
2.6. Statistical analysis
All data obtained are expressed as the mean ± SD. Results were analyzed by a computerized statistical program. Values were compared by one-way ANOVA for multiple comparisons as the post hoc test. A P-value < 0.05 was considered to be statistically significant.
Serum tumor markers in bilharzial and non-bilharzial bladder cancer patients compared to normal (unaffected) patients
1. XO (μmol uric acid/min/ml)
0.3 ± 0.05
2.77 ± 0.33
1.58 ± 0.23
P < 0.0001
2. Fructosamine (μmol/L)
337.88 ± 34.4
1145.27 ± 146.16
742.3 ± 132.44
P < 0.0001
3. hydroxylproline (μg/ml)
23.35 ± 2.83
78.56 ± 10.48
46.06 ± 4.28
P < 0.0001
4. IgE (IU/ml)
44.37 ± 1.66
301.49 ± 14.04
269.0 ± 7.66
P < 0.0001
5. TNF-∝ (Pg/ml)
7.8 ± 0.22
37.7 ± 1.61
24.6 ± 0.84
P < 0.0001
Serum enzymes in bilharzial and non-bilharzial bladder cancerous patients in comparison to healthy persons:
Bilharzial bladder cancerous patients
non-bilharzial bladder cancerous patients
n = 10
n = 4
n = 5
n = 6
n = 6
n = 4
n = 5
Mean ± S.D
28.4 ± 2.3
102.7 ± 6.9
120.6 ± 8.5
132.9 ± 10.1
85.3 ± 4.9
96.5 ± 9.3
107.3 ± 11.6
Mean ± S.D
26.3 ± 1.8
82.2 ± 3.95
96.5 ± 6.1
111.1 ± 9.9
69.3 ± 6.5
83.3 ± 7.6
99.8 ± 6.7
Mean ± S.D
139.9 ± 13.8
351.5 ± 20.2
434.7 ± 21.4
489.3 ± 37.6
334.4 ± 15.5
379.1 ± 14.2
408.6 ± 14.2
Total protein gm%
Mean ± S.D
7.7 ± 0.5
8.30 ± 0.6
8.40 ± 0.4
9.30 ± 0.3
7.40 ± 0.3
7.5 ± 0.4
7.80 + 0.5
Tumor marker enzymes in bilharzial and non-bilharzial carcinoma tissues compared to normal (unaffected) tissues:
Bilharzial bladder cancerous tissues n = 13
Bladder cancerous tissues n = 12
Unaffected (normal) tissues
Unaffected (normal) tissues
Mean ± SD
8.5 ± 0.33
8.8 ± 0.21
9.1 ± 0.12
15.4 ± 0.2
16.3 ± 0.21
17.3 ± 0.17
6.1 ± 0.14
6.9 ± 0.24
7.2 ± 0.17
10.8 ± 0.5
12.5 ± 0.29
13.5 ± 0.3
Mean ± SD
1.74 ± 0.038
1.91 ± 0.01
2.06 ± 0.30
2.85 ± 0.05
3.44 ± 0.1
3.91 ± 0.13
1.61 ± 0.01
1.76 ± 0.04
1.93 ± 0.1
2.78 ± 0.03
3.19 ± 0.02
3.58 ± 0.13
Mean ± SD
4.69 ± 0.04
4.82 ± 0.05
4.98 ± 0.1
7.73 ± 0.3
7.96 ± 0.57
8.22 ± 0.4
4.59 ± 0.05
4.77 ± 0.13
4.86 ± 0.14
7.53 ± 0.02
7.82 ± 0.02
7.97 ± 0.03
Mean ± SD
15.10 ± 3.70
15.21 ± 3.79
15.32 ± 3.81
36.1 ± 10.3
38.4 ± 12.6
42.3 ± 14.7
14.81 ± 3.12
14.97 ± 3.24
15.30 ± 3.51
24.90 ± 4.70
27.0 ± 10.6
30.1 ± 11.34
Essential amino acid fractions in different groups of bladder cancer and bilharzial bladder cancer patients
Bilharzial bladder cancer
2.75 ± 0.390
5.27 ± 1.24
5.3 ± 0.89
5.36 ± 0.397
9.73 ± 2.88
9.99 ± 1.82
7.70 ± 1.175
9.78 ± 3.30
8.3 ± 2.63
3.15 ± 0.83
10.28 ± 4.43
11.6 ± 2.32
3.12 ± 0.46
5.07 ± 1.07
4.7 ± 0.78
5.22 ± 0.58
7.48 ± 1.167
6.7 ± 2.27
8.56 ± 1.43
16.59 ± 3.98
16.9 ± 3.22
1.34 ± 0.39
0.000 ± 0.00
1.5 ± 1.35
2.84 ± 0.58
1.18 ± 0.62
2.1 ± 0.71
Non-essential free amino acid fractions in different groups of bladder cancer and bilharzial bladder cancer patients
Bilharzial bladder cancer
2.61 ± 1.07
5.399 ± 2.230
14.141 ± 10.35
4.46 ± 0.24
14.84 ± 5.37
10.227 ± 3.13
14.14 ± 2.72
9.19 ± 1.22
6.917 ± 4.55
1.09 ± 0.23
19.75 ± 7.43
14.421 ± 3.34
7.98 ± 0.81
12.03 ± 3.15
8.977 ± 2.20
31.38 ± 3.16
35.32 ± 4.64
44.53 ± 14.03
4.23 ± 0.35
5.92 ± 1.91
6.455 ± 0.79
4.23 ± 1.16
9.43 ± 1.94
5.955 ± 2.74
0.19 ± 0.06
0.24 ± 0.086
0.280 ± 0.21
3.35 ± 0.49
6.53 ± 1.69
3.075 ± 0.23
76.5 ± 9.86
88.28 ± 7.24
111.95 ± 9.32
3.22 ± 0.57
3.99 ± 0.81
3.884 ± 1.15
0.96 ± 0.41
1.51 ± 0.36
1.198 ± 0.41
4.396 ± 0.71
11.114 ± 3.42
5.467 ± 0.81
3.58 ± 0.71
7.72 ± 1.23
27.3 ± 3.01
0.0197 ± 0.01
0.188 ± 0.32
0.0010 ± 0.001
1.530 ± 0.29
0.0012 ± 0.002
0.282 ± 0.261
Oxidative stress induces a cellular redox imbalance that has been found to be present in various cancer cells as compared with normal cells, the redox imbalance thus may be related to oncogenic stimulation . The disturbance of the pro-oxidant/antioxidant balance, resulting from increased free radical production, antioxidant enzyme inactivation, and excessive antioxidant consumption, is the causative factor in oxidative damage . There are potentially different types of DNA lesions resulting from ROS and reactive nitrogen species, which could be mutagenic and involved in the etiology of cancer .
Xanthine oxidase (XO: EC 126.96.36.199) is an enzyme playing a part in purine metabolism. It catalyzes the conversion reactions of hypoxanthine to xanthine and xanthine to uric acid, the last reaction in the purine catabolism, with byproduct of toxic superoxide radical. In this regard, it is a key enzyme between purine and free radical metabolism. It was reported that XO is an endogenous source of ROS and reactive nitrogen species (RNS) that can induce oxidative stress and inflect tissue injury [26, 27]. There is growing evidence that superoxide radicals generated by XO are primarily responsible for the cellular deterioration associated with several conditions .
The data reported in the literature on oxidant, antioxidant molecule, and enzymes in different human cancer types are controversial. Our findings show significant increase in XO activity of bilharzial bladder cancer and non-bilharzial bladder cancer patients compared to normal healthy ones. Kokoglu et al.  found higher XO activity in tumoral brain tissues and suggested that the levels of XO in brain tissues could be used as a biochemical marker for the differentiation of tumoral tissues from normal ones. Our findings are consistent with Kaynar et al.  who found an increase in XO activity in patients with small cell and non-small cell lung cancer. Also, Ozturk et al.  observed a significant increase in XO activity in patients with colorectal cancer compared to control group. The authors attributed this increase in this enzyme to an unbalancement alteration in oxidant-antioxidant status due to the cancer process. In addition, Gülec et al.  found that XO activity increased in bladder cancer patients suggested that oxidative stress might be increased in cancerous changes and process, and may affect the course of the disease. The burst of XO-mediated free oxygen radical generation in the cancerous tissue can be triggered by a large increase in substrate formation which occurs secondary to the rapid turn-our of adenine nucleotides during cancer process. On the other hand, as proposed by Durak et al.  high XO activity may be an attempt to lower salvage pathway activity for purines, which is vital for rapid DNA synthesis in cancerous bladder tissue. Moreover, Mohamed et al.  found a significant increase in XO activity in mice infected with S. mansoni parasite.
Given the evidence that supports a relationship between abnormal glucose metabolism and cancer risk, serum fructosamine, one of the markers of abnormal glucose metabolism, is a glycated protein resulting from spontaneous, non enzymatic condensation of glucose and proteins, produces an unstable ketoamine, which is generally referred to as fructosamine due to its structural similarities to fructose [34, 35]. As albumin is the most abundant protein in serum and contains multiple lysine residues, measurement of fructosamine is mainly the determination of glycated albumin . This non enzymatic modification of protein is considered by several authors as a possible common mechanism involved in the progression of many pathological conditions such as myocardial and renal fibrosis, colorectal adenoma and chronic renal failure [35, 37].
The current investigation revealed that there was a highly significant increase in fructosamine level in bilharzial bladder cancer and non-bilharzial bladder cancer patients compared to normal ones. This data is in line with Misciagna et al. [35, 38] who reported that fructosamine is associated with colorectal adenoma. Also, Platek et al.  observed a 60% risk increase for breast cancer in women with high levels of fructosamine, suggesting that fructosamine, as an indicator of glucose consumption, may be a predictor of breast cancer. Recently, Pasanisi et al.  found that fructosamine was not associated with recurrence of breast cancer. Mohamed et al.  reported an increase in serum fructosamine of S. mansoni infected mice, this results was in accordance with our result in case of bilharzial baldder cancer patients. Our results are important because this is the first study investigating serum fructosamine in relation to bladder cancer and may be used as a useful marker for bladder carcinoma risk.
Malignant tumors inhabit a complex carbohydrate metabolism which differs from that of non-neoplastic cells with two main paradigms: 1) malignant cells produce large amounts of lactate even in the presence of sufficient oxygen for aerobic glycolysis. 2) intermediates of the tricarboxylic acid cycle (TCA) are used for fatty, amino and nucleic acid synthesis [41, 42]. Thus, the extensive glucose uptake of cancer cells is needed not only for energy supply but also to provide the components for cellular growth and a high amount of reducing equivalents such as NADPH[41, 42]. To accomplish this, high levels of pyruvate are needed which can be introduced either into the TCA, converted into acetyl-COA or degraded to lactate by LDH[41–43]. By degradation of pyruvate to lactate by LDH, the pool of reductive equivalents on the one hand and the availability of citric acid cycle intermediates for fatty and amino acid synthesis on the other hand is raised. The overexpression of LDH5 in tumor cells supports this theory of a glucose metabolism optimized for cellular growth within malignant tumors.
Results in the present study showed a highly significant increase in LDH activity in both serum and bladder carcinoma tissues of bilharzial bladder and non-bilharzial bladder patients compared to healthy ones. The highest significance was observed in grade III of the disease. These results are in harmony with Kayser et al.  who found that immunohistochemical analysis for LDH5 expression in non-small cell lung cancer (NSCLC) is specific to differentiate malignant neoplasia from healthy lung tissue. The authors reported that LDH5 overexpression in cancer cells induces an upregulated glycolytic metabolism and induced dependence on the presence of oxygen. In addition, Wu et al.  found that the level of LDH was significantly higher in patients with liver metastasis of colorectal cancer than those without liver metastasis.
Another glycolytic enzyme was also estimated in the present study, which is pyruvate kinase enzyme, catalyzing the conversion of phosphoenol pyruvate into pyruvate. Our results revealed significant increase in the activity of PK enzyme in bilharzial and non-bilharzial bladder tissues when compared to the unaffected normal ones. In accordance with our data Shonk et al.  studied the activities of different glycolytic enzymes in carcinoma of rectum and colon and in the corresponding non-malignant counterparts. They observed that glycolytic enzyme activities of the neoplastic tissues of rectum and colon are much higher than the activites in the corresponding normal rectum and colon. Also, Ramo Rao  stated that the glycolytic enzyme pyruvate kinase requires potassium for its maximum activity i.e., the enzyme activity correlates with potassium concentration in tissues or blood. In support, Reddy et al.  expected that the levels of potassium which may be a cofactor for pyruvate kinase should be higher in carcinoma tissues. Recently, Rautray et al.  observed that a potassium level in the carcinoma blood of gallbladder is lower than those in the normal blood samples. Potassium is a major intracellular cation which is also excreted in gastrointestinal tract, sativa, gastric juice, bile, pancreatic and intestinal juices, its deficiency causes acidosis, renal damage and cardiac arrest.
The metabolism of healthy and functionally active cells is optimized for productivity in terms of fulfilling their duty to synthesize, degrade, transport or contract. In contrast to this, malignant tumor cells do not meet these demands but only strive for cellular growth and mitosis . According to this theory high amounts of ATP as demanded within healthy cells are not only not required but act contra - productive for the synthesis of basic elements for cellular growth such as proteins, nucleic acids and fatty acids. Protein is a critical reservoir of metabolic fuel and may become seriously depleted during tumor growth . The metabolism of protein and amino acids in cancer patients is closely linked to glucose metabolism and is regulated by a number of the same hormones and metabolites .
Our findings in the current study showed a slight increase (P < .025) in total protein concentration in serum of bilharzial bladder cancerous patients compared to healthy ones while, there was non-significant decrease in serum total protein of bladder cancer patients when compared to healthy ones. These results are in harmony with Lai et al.  who found that in cancer patients, increased hepatic protein synthesis and gluconeogenesis might lead to a slight decrease in plasma free amino acids levels and a slight increase in plasma protein levels. On contrary to our results, Rossi Fancelli et al.  reported that whole - body protein breakdown has been demonstrated to increase in cancer patients and correlated with gluconeogenesis in malnourished cancer patients.
On the other hand, Sauer and Dauchy,  found that fructose - 1, 6 - disphosphatase, the enzyme involved in the conversion of pyruvate to glucose is elevated in the liver, suggesting that liver protein is utilized for gluconeogenesis in cancer patients. Recently Kojima et al.  detected an elevated proteins in serum of gastric cancer patients with peritoneal dissemination compared with serum samples from patients with gastric cancer in general.
On the contrary of our results, Alexandrakis et al.  found a significant reduction in serum total protein in malignant neoplasms and cirrhotics. Also, Haitel et al.  stated that transitional cell carcinoma and squamous cell carcinoma of the bladder differ in terms of protein expression and prognosis. In addition Ali et al.  found a significant reduction in serum total protein content in bladder cancer, and bilharzial bladder cancer patients compared to the control healthy group and the authors recorded that the decrease was more in bilharzial bladder cancer group than the two other groups.
The data obtained in the current study of diagnostic marker enzymes revealed a marked increase in the activities of aspartate and alanine aminotransferases in serum and tissues of bilharzial bladder cancer and non-bilharzial bladder cancer versus healthy controls and the highest levels in activities of enzymes were obvious in grade III of the bladder cancer.
The increased of AST and ATL levels were more specified extra cellular release and decreased protein content. Several reports confirmed the elevation in AST and ALT activities as a result of S.mansoni infection which may reflect a decrease in hepatic cells, where Salah et al.  and Ahmed  indicated the decrease in hepatic enzymes activities may be due to the release of the enzymes from the necrotic tissue or due to increased cell membrane permiability as a result of relative anoxia and irritation by toxic or metabolic wastes of the worms.
The extra cellular release of the transaminases leads to their increase in serum , while the reduction of enzymes activities relative to lower liver protein content was either due to their release in the bloodstream or due to their decrease synthesis, since transaminases can serve as an index of metabolic aerobity degree, and AST can provide Krebs cycle intermediates, while ALT can be correlated with lactate production . The authors also reported that the elaborated ROS causing damage of cellular membrane, and hence, AST and ALT are sub-cellular enzymes localized in mitochondria and cytoplasm, their release to the bloodstream was increased and their synthesis at the same time decreased.
In accordance with our findings, Ali et al.  who recorded more significant elevation values of AST, ALT in bilharzial and non bilharzial bladder cancer patients compared to normal group. Recently, Wu et al.  found that the levels of ALT and AST were significantly higher in patiens wih liver metastasis of colorectal cancer than in those without liver metastasis.
The amino acids can be classified into two major categories. The essential amino acids are obtained solely from the diet, whereas the body can, under some circumstances, produce non-essential amino acids from other sources. In certain cancers the amino acid profile yields useful data about the disease from which treatment approaches may be better assessed. Colorectal cancer patients exhibit a characteristic amino acid profile: significantly lower taurine, glutamine, valine, and tyrosine in plasma; significantly lower taurine, glutamic acid, methionine and ornithine intracellularly; and elevated valine, isoleucine, leucine, tyrosine, and phenylalanine intracellularly. Obtaining the amino acid profile may help to construct an appropriate dietary manipulation program aimed at modifying intracellular amino acid concentration. Likewise, squamous cell carcinoma of the head and neck exhibit a profile that is marked by decreased taurine, alanine, asparagine, aspartic acid, glycine, histidine, ornithine, phenylalanine, serine, and threonine, with a marked increase in levels of cystine. These features are noted regardless of the stage of the cancer and nutritional status. Thus, serum amino acid levels in serum and other tissues may become a useful cancer marker cancer and provide valuable prognostic information .
Remarkable difference in amino acid profiles between the colorectal cancer patients and the control subjects is found in this study and most of the differences are statistically significant in respect of non-essential amino acids. The difference in essential amino acids concentration was noticeably insignificant except for methionine and theronine. Furthermore, some studies showed that the concentration of amino acids in subjects might be correlated with the same diseases.
The current investigation showed a significant increase in hydroxyproline level in serum of bilharzial bladder cancer and non-bilharzial bladder cancer versus control healthy ones. The increase was more in bilharzial bladder cancer group than the two other groups. In accordance with our data, Proenza et al.  demonstrated an increased levels of hydroxyproline in breast cancer. Also, Mohamed et al.  reported a marked increase in the level of liver hydroxyproline in infected mice versus normal healthy ones. Because collagen is the main element of extracelleular matrix proteins, hydroxyproline, is an amino acid characteristic of collagen metabolism, used as a marker to express the extent of liver fibrosis, as it is the major alteration associated with morbidity . Similar result was obtained by some authors who emphasized that elevated liver hydroxyproline content was associated with S. mansoni infection [67, 68] and this may be attributed to that S. mansoni egg granulomas contain factors reposible for the elevation of free L-hydroxyproline content in the fibrotic liver .
Although IgE is well known for its role in atopic disease and parasitic infections, new evidence suggests that IgE is a pleiotropic Ig molecule with many more functions. Previous studies have shown that IgE possesses antiviral activity, in that IgE anti-HIV-1 antibodies were able to elicit viral clearance and killing through inhibiting virus production .
Data in the present work showed a significant increase in IgE level in bilharzial and non-bilharzial bladder cancer compared to normal group. It is well established that helminthes infestation induces a very high level of serum IgE which is present at both the initial and later stages of schistosomiasis . In western countries where the incidence of parasitic disease is very low, a raised IgE may also occur in some patients with cancer .
In accordance with our findings, Ottesen et al.  indicated that IgE is directed mainly against egg antigen in patients with acute bilharziasis, but it is directed equally to cercarial, egg and adult worm antigens in patients with chronic infestation. In addition, Pidcock et al.  reported that the well established increase in IgE level in patients with schistosomiasis, was also found in bilharzial bladder cancer, indicating that humeral immunity persists in cancer - bearing patients. Patients with cancer not associated with parasitic infestation also had significant increase in their serum level of IgE when compared to healthy Egyptian controls, but 41% of these non-bladder cancer patients showed IgE responses to previous parasitic infestations suggesting that only immunological response to cancer would be on the background of a variable non-specific increase of IgE.
IgE was reported to have the major role in mast cells stimulation which has a central role in the induction of chronic inflammation  and the progression of hepatic fibrosis by producing fibrogenic inflammatory mediators as well as the components of the extracellular matrix proteins (ECMPs) [76, 77]. Elevated IgE levels have been reported in Hodgkin's lymphoma (HL) and advanced stage of HL disease has also been found to be correlated with elevated IgE .
It has been postulated that the association between HL and high serum IgE levels is linked to suppressor lymphocyte dysfunction (CD8+) and is distinct from the increase in allergen - specific IgE, which is associated with atopy . Recently, Fu et al.  reported the presence of elevated IgE and its receptor SCD23 in serum obtained from pancreatic cancer patients versus controls, whereas other Ig isotypes (IgG, IgM, IgA) did not differ between patient and control populations. Also, Chang et al.  reported that high maternal IgE levels were positively associated with childhood leukemia, suggesting that maternal immune function may play a crucial role in the etiology of childhood leukemia.
The current work was also extended to study the inflammatory cytokine, tumor necrosis factor - alpha (TNF-α) in bilharzial and non-bilharzial bladder cancer patients. The data revealed a significant increase in TNF-α level in bilharzial and non-bilharzial bladder cancer patients versus normal controls. These results are in harmony with Wahl and Kleinman,  who found an increase in TNF-α in prostate cancer patients and they attributed this increase in TNF-α level to the increase of the inducible nitric oxide synthase (iNOS) which is one of the major responses of inflammatory component in a neoplastic transformation. As a result nitric oxide (NO) species have been implicated not only in direct damage to cellular components like DNA and proteins, but can also cause changes to the antioxidant defense of a cell along with increased ROS and could be one of the driving factors for promoting prostate cancer . Therefore, in addition to ROS generated by inflammatory cells, uncontrolled tumor cell proliferation in an environment rich in growth factors, activated stroma and tumor associated neo-vascualization, can potentiate and/or promote the development of prostate cancer .
Beside, it was reported that TNF-α essentially functions as a trophic factor for maintaining adult schistosome viability, it is expressed during egg deposition and has a crucial role in the modulation of granulomatous reaction induced by the eggs . Torben and Hailu  stated that increased level of this inflammatory cytokine after egg excretion may be an indication of its effect in complications of schistosomiasis, it capable of inducing tissue injury and fibrosis through inducing ROS production, lipid peroxidation , collagen synthesis other fibrogenic risk factors .
In summary, our results add to exicisting evidence by showing the complexity of the association of bilharzias and bladder cancer. This association seems to be dependent on the repeated infestion of the bladder with S.haematobium parasite. This study compared the profile of the studied biochemical parameters among bilharzial and non bilharzial bladder cancer and normal control subjects. This work is believed to highlight the essential biochemical markers that can be important candidates for bladder cancer diagnosis. In this study, we found that serum fructosamine, as an indicator of glucose consumption, may be a predictor of bladder cancer, also the amino acid, hydroxylproline, as an indicator of liver fibrosis, may be a predictor of bladder cancer risk, in addition, IgE and TNF-α are also may be used as a new immunological markers of bladder cancer.
As a conclusion, increased of all previously mentioned markers in both serum and tissues of patients might be a potentially important findings as an additional diagnostic biochemical tools for bladder cancer.
- Shirai T: Etiology of bladder cancer. Semin Urol. 1993, 3: 113-116.Google Scholar
- Abdulamir AS, Hafidh RR, Kadhim HS, Abubakar F: Tumor markers of bladder cancer: The schistosomal bladder tumors versus non-schistosomal bladder tumors. J Exp Clin Cancer Res. 2009, 28: 27-10.1186/1756-9966-28-27.PubMed CentralView ArticlePubMedGoogle Scholar
- Macvicar AD: Bladder cancer staging. BJU Int. 2000, 68 (1): 111-122.Google Scholar
- Aboul-Nasr AL, Boutrous SG, Hussien MH: Cairo Metropolitan Egypt Cancer Registry, 1978-1979. IARC Sci Publ. 1986, 75: 37-41.Google Scholar
- El-Harvey MA, Amr MM, Abdel-Rahman AB: The epidemiology of schistosomiasis in Egypt: Gharbia Governorate. Am J Trop Med hyg. 2000, 62: 42-48.Google Scholar
- Mostafa MH, Sheweita SA, O'Connor PJ: Relationship between schistosomiasis and bladder cancer. Clin Microbiol Rev. 1999, 2: 97-111.Google Scholar
- El-Sebai I: Parasites in the etiology of cancer; bilharziasis and bladder cancer. CA Cancer J Clin. 1977, 27: 100-106. 10.3322/canjclin.27.2.100.View ArticleGoogle Scholar
- Yalcin O, Karatas F, Erulas FA: The levels of glutathione peroxidase, vitamins A, E, C, and lipid peroxidation in patients with urothelial carcinoma of the bladder. BJU Int. 2004, 93: 863-866. 10.1111/j.1464-410X.2003.04729.x.View ArticlePubMedGoogle Scholar
- Arikan S, Akcay T, Konukoglu D: The relationship between antioxidant enzymes and bladder cancer. Noeoplasma. 2005, 52: 314-317.Google Scholar
- Kumar B, Koul S, Khandrika L: Oxidative stress is inherent in prostate cancer cells and is required for aggressive phenotype. Cancer Res. 2008, 68: 1777-1785. 10.1158/0008-5472.CAN-07-5259.View ArticlePubMedGoogle Scholar
- Barzilai A, Rotman G, Shiloh Y: ATM deficiency and oxidative stress: a new dimension of defective response to DNA damage. DNA Repair. 2002, 22: 3-25.View ArticleGoogle Scholar
- Pelicano H, Carney D, Huang P: ROS stress in cancer cells and therapeutic implications. Drug Resistance Updates. 2004, 7: 97-110. 10.1016/j.drup.2004.01.004.View ArticlePubMedGoogle Scholar
- Naka K, Muraguchi T, Hoshii T, Hirao A: Regulation of reactive oxygen species and genomic stability in hematopoietic stem cells. Antioxid Redox Signal. 2008, 10: 1883-1894. 10.1089/ars.2008.2114.View ArticlePubMedGoogle Scholar
- Nishikawa M: Reactive oxygen species in tumor metastasis. Cancer Lett. 2008, 266: 53-59. 10.1016/j.canlet.2008.02.031.View ArticlePubMedGoogle Scholar
- Khandrika L, Kumar B, Koul S, Maroni P, Koul HK: Oxidative stress in prostate cancer. Cancer Letters. 2009, 282: 125-136. 10.1016/j.canlet.2008.12.011.PubMed CentralView ArticlePubMedGoogle Scholar
- Fried R, Fried LW: Xanthine oxidase (xanthine dehydrogenase). Methods of Enzymatic Analysis. Edited by: Bergmeyer HU. 1974, Verlag Chemie, Weinheim, Academic Press, London, 2: 644-649. 2View ArticleGoogle Scholar
- Parlin D, Whelan J, Ferlay L, Raymond L, Young J, editors : 1997, IARC, Scientific Publications
- Lowry OH, Rosenbrough NJ, Farral AL, Randall RJ: Protein measurement with the folin phenol reagent. J Biol Chem. 1951, 193 (1): 265-275.PubMedGoogle Scholar
- Jamall IS, Finelli VN, QueHee SS: A simple method to determine nanogram levels of 4-hydroxyproline in biological tissues. Anal Biochem. 1981, 112: 7075-View ArticleGoogle Scholar
- Nabih I, El-Ansary A, Abdel-Galil F, Zayed N: On the factors controlling metabolic integration between schistosoma parasites and their molluscan hosts. J Egyp Ger Soc Zool Invert Zool Parasitol. 1998, 26D: 87-102.Google Scholar
- Caboud PG, Wroblewski F: Colorimetric measurement of lactic dehydrogenase activity of body fluids. Am J Clin Phathol. 1958, 30 (3): 234-236.Google Scholar
- Ibsen KH, Orlando RA, Garratt KN, Hernandez AM, Giorlando S, Nungaray G: Expression of multimolecular forms of pyruvate kinase in normal, benign, and malignant human breast tissue. Cancer Research. 1982, 42 (3): 888-892.PubMedGoogle Scholar
- Valko M, Rhodes CJ, Moncol J: Free radicals, metals, and antioxidants in oxidative stress - induced cancer. Chem Biol Interact. 2006, 160: 1-40. 10.1016/j.cbi.2005.12.009.View ArticlePubMedGoogle Scholar
- Aymelek G, Erten D, Aslan S: Lipid peroxidation and antioxidant status in blood and tissue of malignant breast tumor and benign breast disease. Cell Biol Int. 2006, 30: 376-380. 10.1016/j.cellbi.2006.02.005.View ArticleGoogle Scholar
- Beevi SS, Rasheed MH, geetha A: Evidence of oxidative and nitrosative stress in patients with cervical squamous cell carcinoma. Clin Chim Acta. 2007, 375: 119-132. 10.1016/j.cca.2006.06.028.View ArticlePubMedGoogle Scholar
- Mohamed AA, Abo-Amou DE, Shehata MA, El-Ashery NE: Glutathione peroxidase and nitric oxide in patients with chronic liver diseases. Egypt J Schistosomiais Infect Endem Dis. 2001, 23: 27-46.Google Scholar
- Harrison R: Structure and function of xanthine oxidoreductase: where are we now?. Free Radic Biol Med. 2002, 33: 774-797. 10.1016/S0891-5849(02)00956-5.View ArticlePubMedGoogle Scholar
- Gülec M, Akin H, Yüce H, Ergin E, Elyas H, Yalcin O, Akyol O: Adenosine deaminase and xanthine oxidase activities in bladder washing fluid from patients with bladder cancer: a preliminary study. Clin Biochem. 2003, 36: 193-196. 10.1016/S0009-9120(02)00452-6.View ArticlePubMedGoogle Scholar
- Kokoglu E, Belce A, Ozyurt E, Tepeler Z: Xanthine oxidase levels in human brain tumors. Cancer Lett. 1990, 50: 179-181. 10.1016/0304-3835(90)90262-V.View ArticlePubMedGoogle Scholar
- Kaynar H, Meral M, Turhan H, Keles M, Celik G, Akcay F: Glutathione peroxidase, glutathione - S - transferase, catalase, xanthine oxidase, Cu-Zn superoxide dismutase activities, total glutathione, nitric oxide and malondialdehyde levels in erythrocytes of patients with small cell and non-small cell lung cancer. Cancer Letters. 2005, 227: 133-139. 10.1016/j.canlet.2004.12.005.View ArticlePubMedGoogle Scholar
- Ozturk HS, Karaayvaz M, Kacmaz M, Kavutcu M, Akgul H, Durak I: Activities of the enzymes participating in purine and free-radical metabolism in cancerous human colorectal tissues. Cancer Biochem Biophys. 1998, 16: 157-168.PubMedGoogle Scholar
- Durak I, Isik ACU, Canbolat O, Akyol O, Kavutcu M: Adenosine deaminase, 5 nucleotidase, xanthine oxidase, superoxide dismutase and catalase activities in cancerous and non-cancerous human laryngeal tissues. Free Radic Biol Med. 1993, 15: 681-4. 10.1016/0891-5849(93)90174-S.View ArticlePubMedGoogle Scholar
- Mohamed AM, Mahmoud SS, Farrag RA: Influence of sativa seeds against liver fibrosis and consequence complications in murine schistosomiasis. Int J Biotech and Biochem. 2008, 4 (4): 325-346.View ArticleGoogle Scholar
- Saydah S, Loria C, Eberhardt M, Brancati F: Abnormal glucose tolerance and the risk of cancer death in the United State. Am J Epidemiol. 2003, 157: 1092-1100. 10.1093/aje/kwg100.View ArticlePubMedGoogle Scholar
- Misciagna G, De Michele G, Guerra V, Cisternino AM, Di Leo A, Freudenheim JL: Serum fructosamine and colorectal adenomas. Eur J Epidemoil. 2004, 19: 425-432.View ArticleGoogle Scholar
- Lapolla A, Traldi P, Fedele C: Importance of measuring product of non-enzymatic glycation of proteins. Clin Biochem. 2005, 38: 103-115. 10.1016/j.clinbiochem.2004.09.007.View ArticlePubMedGoogle Scholar
- Vijayan G, Sundaram RC, Bobby Z, Hamide A, Selvaraj N, Dasse NR: Increased plasma malondialdehyde and fructosamine in anemic H pylori infected patients: Effect of treatment. World J Gastroenterol. 2007, 13: 796-800.PubMed CentralView ArticlePubMedGoogle Scholar
- Misciagna G, Caruso MG, Trevisan M: Nutrition, metabolism and colorectal cancer. Genes Nutr. 2008, 3: 15-17. 10.1007/s12263-008-0080-7.PubMed CentralView ArticlePubMedGoogle Scholar
- Platek M, Krogh V, Micheli A, Browne R, Meneghini E, Sieri S, Schunemann HJ, Pala V, Barba M, Wilding GE, Berrino F, Muti P: Serum fructosamine and subsequent breast cancer risk: A nested case-control study in the ORDET prospective cohort study. Cancer Epidemiol Biomarkers Prev. 2005, 14 (1): 271-274.PubMedGoogle Scholar
- Pasanisi P, Venturelli E, Morelli D, Fontana L: Serum insulin - like growth factor-1 and platelet - derived growth factor as biomarkers of breast cancer prognosis. Cancer Epidemiol Biomarkers Prev. 2008, 17 (7): 1719-1722. 10.1158/1055-9965.EPI-07-0654.View ArticlePubMedGoogle Scholar
- DeBerardinis RJ, Lum JJ, Hatzivassilliou G, Thompson CB: The biology of cancer, metabolic reprogramming fuels, cell growth and proliferation. Cell Metabolism. 2008, 7: 11-20. 10.1016/j.cmet.2007.10.002.View ArticlePubMedGoogle Scholar
- DeBerardinis RJ, Sayed N, Ditsworth D, Thompson CB: Brick by brick: metabolism and tumor cell growth. Current Opinion in Genetics and Development. 2008, 18: 54-61. 10.1016/j.gde.2008.02.003.PubMed CentralView ArticlePubMedGoogle Scholar
- Coy JF, Dressler D, Wilde J, Schubert P: Mutations in the transketolase-link gene TKTL1: Clinical implications for neurode generative diseases, diabetes and cancer. Clinical Laboratory. 2005, 5: 257-273.Google Scholar
- Kayser G, Kassem A, Sienel W, Uentrop LS, Mattern D, Aumann K, Stickeler E, Werner M, Passlick B, Hausen AZ: Lactate - dehydrogenase 5 is overexpressed in non-small cell lung cancer and correlates with the expression of the transketolase - like protein 1. Diagnostic Pathology. 2010, 5: 22-31. 10.1186/1746-1596-5-22.PubMed CentralView ArticlePubMedGoogle Scholar
- Wu XZ, Ma F, Wang XL: Serological diagnostic factors for liver metastasis in patients with colorectal cancer. World J Gastroenterology. 2010, 16 (32): 4084-4088. 10.3748/wjg.v16.i32.4084.View ArticleGoogle Scholar
- Shonk CE, Majima H, Koven BJ, Boxer GE: Enzyme patterns in human tissues IV: comparison of glycolytic enzymes in surgical biopsies and autopsy specimens. Cancer Res. 1966, 26: 607-PubMedGoogle Scholar
- Rama Rao AVSS: A text Book f Biochemistry. 2002, L.K. and S Publishers, 438-Google Scholar
- Reddy SB, Charle MJ, Raju GJN, Vijayan V, Reddy BS, Kumar MR, Sundareswar B: Trace elemental analysis of carcinoma kidney and stomach by PIXE method. Nucl Instr and Meth. 2003, B 207: 345-View ArticleGoogle Scholar
- Rautray TR, Vijayan V, Sudarshan M, Panigrahi S: Analysis of blood and tissue in gallbladder cancer. Nuclear Instruments and Methods in Physics Research B. 2009, 267: 2878-2883. 10.1016/j.nimb.2009.06.084.View ArticleGoogle Scholar
- Lai HS, Lee JC, Lee PH, Wang ST, Chen WJ: Plasma free amino acid profile in cancer patients. Seminars in Cancer Biology. 2005, 15: 267-276. 10.1016/j.semcancer.2005.04.003.View ArticlePubMedGoogle Scholar
- Heber D, Tchekmedyian NS: Cancer cachexia and anorexia. Nutritional oncology. Edited by: Heber D, Blackburn GL, Go VLW. 1999, California, Academic Press, 537-546.Google Scholar
- Rossi Fanelli F, Cangiano C, Muscaritoli M, Conversano L, Torelli GF, Cascino A: Tumor - induced changes in host metabolism: a possible marker of neoplastic disease. Nutrition. 1995, 11: 595-600.PubMedGoogle Scholar
- Sauer LA, Dauchy RT: Pathways of energy metabolism in cancer. Nutrition and cancer prevention. Edited by: Watson RR, Mufti SI. 1996, Florida: CRC Press, 128-136.Google Scholar
- Kojima T, Yoshikawa K, Saga S, Yamada T, Kure S, Matsui T, Uemura T, Fujimitsu Y, Sakakibara M, Kodera Y, Kojima H: Detection of elevated proteins in peritoneal dissemination of gastric cancer by analyzing mass spectra data of serum proteins. Journal of Surgical Research. 2009, 155: 13-17. 10.1016/j.jss.2008.07.024.View ArticlePubMedGoogle Scholar
- Alexandrakis MG, Moschandrea J, Kyriakoy DS, Alexandraki R, Kouroumalis E: Use of a variety of biological parameters in distinguishing cirrhotic from malignant ascites. J Biol Markers. 2001, 16: 45-49.Google Scholar
- Haitel A, Posch B, El-Baz M, Mokhtar AA, Susani M, Ghoneim MA, Marberger M: Bilharzial related, organ confined, muscle invasive bladder cancer prognostic value of apoptoisis marker, proliferation markers, P 53, E-Cadherin, epidermal growth factor receptor and Cerb B-2. J Urol. 2001, 165: 1481-10.1016/S0022-5347(05)66332-X.View ArticlePubMedGoogle Scholar
- Ali SA, Saba El-Rigal N, Ahmed SA, Khaled HM: Biochemical alterations in serum of bladder cancer patients with and without schistosomiasis. J Genetic Eng and Biotechnol. 2005, 3 (1): 59-71.Google Scholar
- Salah LA, Kheireldin AA, Mansour MM, Hussein F: Levels of some serum enzymes in patients with schistosomiasis. Am J Trop Med Hyg. 1976, 79: 270-277.Google Scholar
- Ahmed SA: Serum alkaline phosphatase activity during pregnancy and post-partum period in bilharzial Egyptian patients. Egypt J Pharm Sc. 1994, 35: 605-611.Google Scholar
- Ozacan A, Mengil A: Effect of oral ethanol treatment on the gamma- GT, ALT and AST enzyme activities in the serum, liver and kidneys and on some total cholesterol and lipid levels in rats. Tur Veterinelik - Ve - Hayvan - Cilik - Dergisi. 1998, 22: 181-187.Google Scholar
- Ozares R, Tahan V, Aydin S, Uzun H, Kaya S, Senturk H: N-acetyl-cysteine attenuates alcohol - induced oxidative stress in rats. World J Gastroentrol. 2003, 9: 791-798.Google Scholar
- Vecer J, Kvapil M, Sprongl L, Kubátová H, Hoch J, Jech Z, Charvát J: Tissue amino acids in patients with colorectal carcinoma. Vnitr Lek. 1998, 44 (4): 192-4.PubMedGoogle Scholar
- Scioscia KA, Snyderman CH, Wagner R: Altered serum amino acid profile in head and neck cancer. Nutr Cancer. 1998, 30: 144-7. 10.1080/01635589809514654.View ArticlePubMedGoogle Scholar
- VanderJagt DJ, Kanellis GJ, Isichei C, Pastuszyn A, Glew RH: Serum and urinary Amino acid levels in sickle cell disease. J Trop Pediatrics. 1997, 43: 220-225. 10.1093/tropej/43.4.220.View ArticleGoogle Scholar
- Proenza AM, Oliver J, Palou A, Roca P: Breast and lung cancer are associated with a decrease in blood cell amino acid content. J Nutr Biochem. 2003, 14: 133-138. 10.1016/S0955-2863(02)00225-5.View ArticlePubMedGoogle Scholar
- Souza ALS, Roffe E, Pinho V, Souza DG, Silva AF, Russo RC, Guabiraba R, Pereira CAJ, Carvalho FM, Barsante MM, Oliveira RC, Fraga LAO, Correa DN, Teixeira MN: Potential role of the chemokine macrophage inflammatory protein 1 α in human and experimental schistosomiais. Infection and Immunity. 2005, 73: 2515-2523. 10.1128/IAI.73.4.2515-2523.2005.PubMed CentralView ArticlePubMedGoogle Scholar
- Marck EV: The Therapeutic effect of the neuropeptide hormone somatostatin on Schistosoma mansoni caused liver fibrosis. BMC Infectious Diseases. 2005, 5: 45-10.1186/1471-2334-5-45.PubMed CentralView ArticlePubMedGoogle Scholar
- Metwally NS: Potency of Allium sativun and Allium cepa oils against Schistosoma mansoni infection in mice. Egypt J Hospital Med. 2006, 23: 319-332.Google Scholar
- Potter JJ, Tankesley LR, Mezey E: Infuence of leptin in the development of hepatic fibrosis produced in mice by Schistosoma mansoni infection and by chronic carbon tetrachloride administration. J Hepatol. 2003, 38: 281-288.View ArticlePubMedGoogle Scholar
- Pellegrino MG, Bluth MH, Smith Norowitz T: HIV type 1-specific IgE in serum of long - term surviving children inhibitis HIV type 1 production in vitro. AIDS Res Hum Retroviruses. 2002, 18: 363-372. 10.1089/088922202753519142.View ArticlePubMedGoogle Scholar
- Iskander R, Das PK, Aalberse RC: IgG4 antibodies in Egyptian patients with schistosomiais. Int Arch Allergy Appl Immunol. 1981, 66: 200-207. 10.1159/000232819.View ArticlePubMedGoogle Scholar
- Hallgren R, Arrendal H, Hiesche K, Lundquist G, Nou E, Zotterstrom O: Elevated serum immunoglobulin E in bronchial carcinoma: its relation to the histology and prognosis of the cancer. J Allergy Clin Immunol. 1981, 67: 398-406. 10.1016/0091-6749(81)90086-5.View ArticlePubMedGoogle Scholar
- Ottesen EA, Poinexter RW, Hussain R: Detection, quantitation and specificity of antiparasite IgE antibodies in human schistomiasis mansoni. Am J Trop Med Hyg. 1981, 30: 1228-1237.PubMedGoogle Scholar
- Pidcock NB, Cooper EH, El-Aaser AA, El-Sebai I: Immunoglobulin A, G and E levels in Egyptians with cancer: influence of schistosomiasis. Int J Cancer. 1984, 33: 771-775. 10.1002/ijc.2910330610.View ArticlePubMedGoogle Scholar
- Jayapal M, Tay HK, Reghunathan R, Zhi L, Chow KK, Rauff M, Melendez AJ: Genome - wide gene expression profiling of human mast cells stimulated by IgE or FCw RI-aggregation reveals a complex network of genes involved in inflammatory responses. BMC Genomics. 2006, 7: 201-227. 10.1186/1471-2164-7-201.View ArticleGoogle Scholar
- Gruber BL: Mast cells in the pathogenesis of fibrosis. Curr Rheumatol Rep. 2003, 5: 147-153. 10.1007/s11926-003-0043-3.View ArticlePubMedGoogle Scholar
- Shen DZ: A target role for mast cell in the prevention and therapy of hepatic fibrosis. Medical Hypotheses. 2008, 70: 760-764. 10.1016/j.mehy.2007.07.042.View ArticlePubMedGoogle Scholar
- Rubinstein E, Sokal JR, Reisman RE, Arbesman C: Relationship of serum total IgE and cell mediated immunity in patients with Hodgkin's disease. Int Arch Allergy Appl Immunol. 1977, 55: 439-443. 10.1159/000231955.View ArticlePubMedGoogle Scholar
- Eckschlager T, Prusa R, Hladi Rova M, Radvanska J, Slaby K, Radvansky J: Lymphocyte subpopulations and immunoglobulin levels in Hodgkin's disease survivors. Neoplasma. 2004, 51: 261-264.PubMedGoogle Scholar
- Fu SL, Pierre J, Smith-Norowitz TA, Hagler M, Bowne W, Pincus MR, Mueller CM, Zenilman ME, Bluth MH: Immunoglobulin E antibodies from pancreatic cancer patients mediate antibody - dependent cell - mediated cytotoxicity against pancreatic cancer cells. Clinical and Experimental Immunology. 2008, 153: 401-409. 10.1111/j.1365-2249.2008.03726.x.PubMed CentralView ArticlePubMedGoogle Scholar
- Chang JS, Buffler PA, Metayer C, Chokkalingam AP, Patokol J, Kronish D, Wiemeles JL: Maternal immunoglobulin E and childhood leukemia. Cancer. Epidemiol Biomarkers Prev. 2009, 18 (8): 2221-2227. 10.1158/1055-9965.EPI-09-0212.View ArticleGoogle Scholar
- Wahl LM, Kleinman HK: Tumor - associated macrophages as targets for cancer therapy. J NaH Cancer Inst. 1998, 90: 1583-1584. 10.1093/jnci/90.21.1583.View ArticleGoogle Scholar
- Palapatt GS, Sutcliffe S, Bastian PJ, Platz EA, Dc Marzo AM, Lsaacs WB, Nelson WG: Prostate carcinogenesis and inflammation: emerging insights. Carcinogenesis. 2005, 26: 1170-1181.View ArticleGoogle Scholar
- Araldi EM, Dellaica , Sogno I, Lorusso G, Garbisa S, Albini A: Natural and synthetic agents targeting inflammation and angiogenesis for chemoprevention of prostate cancer. Curr Cancer Drug Targets. 2008, 8: 146-155. 10.2174/156800908783769382.View ArticlePubMedGoogle Scholar
- Haseeb MA, Shirazian DJ, Preis J: Elevated serum levels of TNF-alpha, Stnf-RII in murine schistosomiasis correlate with schistosome oviposition and circumoval granuloma formation. Cytokine. 2001, 15: 266-269. 10.1006/cyto.2001.0925.View ArticlePubMedGoogle Scholar
- Torben W, Hailu A: Serum cytokines of the 20 k rad-irradiated Schistosoma mansoni cercariae vaccinated, primary and superinfected Cercopethicus aethiops. Exp Parasitol. 2007, 115: 121-126. 10.1016/j.exppara.2006.07.004.View ArticlePubMedGoogle Scholar
- Poli G: Pathogenesis of liver fibrosis: role of oxidative stress. Mol Aspects Med. 2000, 21: 49-98. 10.1016/S0098-2997(00)00004-2.View ArticlePubMedGoogle Scholar
- Booth M, Vennervald BJ, Butterworth AE, Kariuki C, Amaganga C, Kimani G, Mwatha JK, Oteda A, Ouma JH, Dunne DW: Exposure to malaria affects the regression of hepatospleenomegaly after treatment for Schistosoma mansoni infection in Kenyan. BMC Medicine. 2004, 2: 36-45. 10.1186/1741-7015-2-36.PubMed CentralView ArticlePubMedGoogle Scholar
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