- Primary research
- Open Access
Expression and subcellular localization of Discoidin Domain Receptor 1 (DDR1) define prostate cancer aggressiveness
Cancer Cell International volume 21, Article number: 507 (2021)
The Discoidin Domain Receptor 1 (DDR1) is one of the two members of a unique family of receptor tyrosine kinase receptors that signal in response to collagen, which has been implicated in cancer progression. Here, we examined the expression of DDR1 in prostate cancer (PCa), and assessed its potential value as a prognostic marker, as a function of grade, stage and other clinicopathologic parameters.
We investigated the association between the expression level and subcellular localization of DDR1 protein and PCa aggressiveness by immunohistochemistry, using tissue microarrays (TMAs) encompassing 200 cases of PCa with various Gleason scores (GS) and pathologic stages with matched normal tissue, and a highly specific monoclonal antibody.
DDR1 was found to be localized in the membrane, cytoplasm, and nuclear compartments of both normal and cancerous prostate epithelial cells. Analyses of DDR1 expression in low GS (≤ 7[3 + 4]) vs high GS (≥ 7[4 + 3]) tissues showed no differences in nuclear or cytoplasmic DDR1in either cancerous or adjacent normal tissue cores. However, relative to normal-matched tissue, the percentage of cases with higher membranous DDR1 expression was significantly lower in high vs. low GS cancers. Although nuclear localization of DDR1 was consistently detected in our tissue samples and also in cultured human PCa and normal prostate-derived cell lines, its presence in that site could not be associated with disease aggressiveness. No associations between DDR1 expression and overall survival or biochemical recurrence were found in this cohort of patients.
The data obtained through multivariate logistic regression model analysis suggest that the level of membranous DDR1 expression status may represent a potential biomarker of utility for better determination of PCa aggressiveness.
The Discoidin Domain Receptors (DDRs) belong to the family of receptor tyrosine kinases (RTKs) that signal in response to collagen, the major component of extracellular matrices. Whereas the majority of the ligands for RTKs are soluble diffusible proteins, the DDRs are the only receptors that recognize collagens as ligands [1, 2]. Upon binding to collagen, DDRs undergo phosphorylation in their intracellular domains [3, 4], which activate downstream effectors to initiate signaling pathways that control cell fate and behavior. Thus, DDRs are major mediators of cell–matrix interactions.
The DDR family is comprised of two members, DDR1 and DDR2, which are encoded by two distinct genes located in different chromosomes . While there is only one DDR2 form, the DDR1 subfamily of receptors is comprised of five isoforms generated by alternative splicing from which three are fully functional kinases (DDR1a, DDR1b, and DDR1c), and two are truncated receptors (DDR1d and DDR1e) lacking enzymatic activity. At present, the cellular distribution and functional roles of each DDR1 isoform in different tissues remain unclear. DDR1 is usually expressed by epithelium whereas DDR2 is mostly expressed by mesenchymal cells. However, this distinction is not clearly maintained during pathological conditions [1, 5]. Structurally, both DDRs are type I transmembrane proteins and have a characteristic N-terminal extracellular domain that is homologous to the Dictyostelium discoideum N-acetylgalactosamine-binding lectin Discoidin-I, referred to as Discoidin domain (DS), which mediates binding to collagens. The DS domain is followed by a DS-like domain, an extracellular juxtamembrane region, a transmembrane region, and an intracellular cytoplasmic region that contains the kinase domain at the C-terminus [2, 6]. DDRs undergo receptor activation by both non-fibrillar and fibrillar collagens as their ligands, DDR1 recognizing both types of collagens, whereas DDR2 mostly fibrillar collagens. DDR1 is uniquely activated by collagen IV, and thus DDR1 can mediate the interactions of epithelial cells with the basement membrane. Another feature that sets the DDRs apart from other RTKs is their delayed and long-lasting phosphorylation upon binding to their ligands [2, 7].
An increasing number of studies suggest a pivotal role of DDRs in cancer progression [5, 8,9,10]. Levels of DDRs are usually elevated in a variety of cancer types, which have been associated with malignant progression and poor patient survival [5, 8, 10,11,12,13,14]. Consistently, findings in experimental models of cancer have shown that DDRs play a key role in tumorigenesis and metastatic ability [15,16,17,18,19,20,21,22,23]. Therefore, DDRs are considered promising therapeutic targets in various cancer types, and several small molecules kinase inhibitors of DDRs have been developed [24,25,26].
Prostate cancer (PCa) is the most commonly diagnosed non-skin malignant neoplasia in males in the United States . Despite the management of the disease when still confined to the gland with local therapies such as radical prostatectomy (RP), endocrine, and radiation therapy (RT), not all patients can be definitively cured. In fact, 20–40% of patients treated with RP [28, 29] and 30–50% of those treated with RT  experience rising serum prostate-specific antigen (PSA) levels—a condition known as biochemical recurrence (BCR)—within 10 years. Although progression to metastases occurs in some patients after BCR, the latter is not considered a surrogate for metastatic disease or PCa-specific mortality [31, 32]. Conversely, Gleason score (GS) remains one of the strongest pathologic indicators of PCa aggressiveness, with a GS of 6 or below indicating a lower risk of PCa-specific mortality and a GS of 8 or above indicating a higher risk . However, prognosis prediction in patients with GS 7 prostate tumors, designed as “intermediate risk PCas”, is challenging due to a marked heterogeneity of clinical outcomes that may result from an actual difference in aggressiveness between Gleason 3 + 4 = 7 and 4 + 3 = 7 tumors [34,35,36], now referred to as Grades Group 2 and 3, respectively [37, 38]. Therefore, the identification of novel molecular markers that may improve risk stratification and lead to novel therapies for certain PCa patients is critically needed. A few studies examined the expression of DDR1  and DDR2  in PCa tissues. DDR1 protein was found to be expressed in PCa clinical specimens and correlated with androgen-independence, but not associated with GS score or PSA levels . High DDR2 expression in advanced PCa was found to strongly correlate with PSA, GS, and lymph node metastasis . In the present study, we utilized a highly specific and validated monoclonal antibody to human DDR1 that was specifically developed for immunohistochemistry (IHC) analyses [41, 42]. Using this antibody, we evaluated the expression of DDR1 in various subcellular fractions (membrane, cytoplasm, and nucleus) in a cohort of PCa samples with tumor and adjacent normal epithelium that, to our knowledge, is the largest set of PCa specimens studied for this RTK up to date. Specifically, we assessed the association between DDR1 expression and subcellular localization and PCa aggressiveness, and its potential value as a prognostic marker, as a function of grade, stage and other clinicopathologic parameters.
Materials and methods
Prostate tissue specimens
The Grade/Stage tissue microarray (TMA) slides containing de-identified human PCa specimens were obtained from the Prostate Cancer Biorepository Network (PCBN), a public bioresource for PCa investigators funded by the Department of Defense resulting from a collaboration between Johns Hopkins University and New York University School of Medicine (Provider Investigator: Dr. Bruce Trock, Johns Hopkins University, Baltimore, MD). Five TMAs referred to as TMA 18, 19, 22, 24, and 34 containing 1,600 cores obtained from radical prostatectomies performed in PCa patients were analyzed in our study. The TMAs comprise a total of 200 cases of PCa with various GS and pathology stages represented in quadruplicate cores, and matching non-cancerous prostate tissues referred to as “normal” (also 4 cores per case). All subjects were annotated based on age, race, treatments received after radical prostatectomy, biopsy GS, serum PSA levels at diagnosis, clinical stage (T) as defined by the American Joint Committee on Cancer (Table 1), and occurrence of BCR (increase of postoperative serum PSA level to 0.2 ng/ml) (Additional file 1: Table S1). None of the patients received preoperative therapy (chemo-, radio- or hormonal therapy).
TMA sections were deparaffinized with xylene and rehydrated with decreasing percentages of ethanol (100% to 70%). Unmasking of antigenic epitopes was performed with Antigen Retrieval Citrus Plus Solution (Cat. # HK0805K, BioGenex, Fremont, CA) in a pressure cooker placed in a microwave for two cycles of 15 min at heat levels 5 and 2. After 20 min at room temperature, the sections were washed with phosphate-buffered saline (PBS) and endogenous peroxidase quenched with 3% hydrogen peroxide in PBS for 30 min. After washing with PBS and blocking of non-specific binding sites with 2.5% normal horse serum for 20 min at room temperature, the tissues were incubated with an in-house raised rabbit monoclonal antibody (mAb) against the extracellular domain of human DDR1  referred to as Rab‑819 antibody, at a 1:100 dilution (from a stock solution of 1 mg/ml) overnight at 4 °C. Immunostaining was performed by incubation with a peroxidase micropolymers attached to anti-rabbit IgG made in horse (Cat. # MP-7401, ImmPRESS™, Vector Laboratories, Burlingame, CA) for 30 min at room temperature, followed by detection with ImmPACT™ DAB peroxidase substrate (Cat. # SK-4105, Vector Laboratories) and light nuclear counterstaining with Mayer’s hematoxylin (Cat. # HMM500, ScyTek Laboratories, Logan, UT). DDR1 immunoreactivity was evaluated and reported by two independent pathologists (SV and DS) as positive or negative staining in different subcellular localizations (i.e., plasma membrane, nucleus, and cytoplasm) in cancerous and adjacent normal (no evidence of neoplastic changes) tissues. For membrane immunostaining, only full membranous staining was considered positive, whereas no staining or staining at basal or basolateral locations were defined as negative.
The human PCa PC-3 and C4-2B cell lines were purchased from the American Type Culture Collection (ATCC). Normal human prostate epithelial cell lines, CF-91, ML-8891, CLR-2221, RWPE-1, RWPE-2, and benign prostatic hyperplasia (BPH) epithelial cell lines were kindly provided by Dr. S. Sheng [Wayne State University (WSU)], whereas human PCa LNCaP and DU145 cell lines were supplied by Dr. H-R.C. Kim (WSU). Normal prostate epithelial cell lines, CF-91, ML-8891, CLR-2221, RWPE-1, RWPE-2 were maintained in Keratinocyte Serum Free Medium (Cat. # 17005042, Thermo Fisher Scientific, Waltham, MA.) supplemented with 0.05 mg/ml bovine pituitary extract and 5 ng/ml epidermal growth factor. PC3, LNCaP and C4-2B cell lines were maintained in RPMI-1640 Medium, HEPES (Cat. # 22400121 Thermo Fisher Scientific), supplemented with 10% Fetal Bovine Serum (FBS) (Cat. # 16000044, Thermo Fisher Scientific). The DU145 cell line was cultured in DMEM Medium (Cat. # 10313039, Thermo Fisher Scientific) supplemented with 10% FBS and 1% Penicillin–Streptomycin solution. All the human cell lines used were periodically confirmed negative for mycoplasma contamination and authenticated through short tandem repeat profiling by the Research Technology Support Facility of Michigan State University.
Immunoblot analyses, collagen stimulation, and cell fractionation
For analyses of DDR1 expression in whole cell lysates, cultured prostate epithelial cells were lysed in RIPA buffer (50 mM Tris–HCl, pH 7.4, 150 mM NaCl, 1% NP-40, 0.25% sodium deoxycholate and 1 mM EDTA) supplemented with protease inhibitors Cocktail, EDTA-free (Cat. # 539134, Sigma-Aldrich, St. Louis, MO) and 10 mM sodium fluoride and 1 mM sodium orthovanadate. The cell lysates were cleared by centrifugation at 13,000g at 4 °C for 15 min, and the protein concentration was determined using the BCA kit from Pierce (Cat. # 23227, Waltham, MA). Equal amounts of protein from each lysate were resolved by reducing 7.5% SDS-PAGE. Proteins were then transferred to a nitrocellulose membrane using conventional methods. The blots were probed with anti-DDR1 polyclonal antibody Sc-532 (Santa Cruz Biotechnology, Inc. Dallas, Texas), which recognizes a DDR1 epitope at the C-terminal end of the receptor. For loading control, the same blot was reprobed with anti-β-actin antibody.
For analyses of DDR1 subcellular localization in malignant (PC-3) and non-malignant (RWPE-1) cells as a function of collagen stimulation, cells were washed twice with PBS and incubated in serum-free media, overnight. The cells were then treated with 20 µg/ml rat tail collagen type I (Cat. # 354236, Discovery Labware Inc., Corning™, Bedford, MA) for 90 min at 37 °C, washed twice with cold PBS and then gently dissociated from the plates using Cell Dissociation Buffer (Cat. # 13151014, Thermo Scientific). The cytoplasmic/membrane and nuclear fractions were isolated using the NE-PER Nuclear Cytoplasmic Extraction Reagent kit (Cat. # 78833, Thermo Scientific, Grand Island, NY, USA), according to the manufacturer’s instruction. Cytoplasmic and nuclear extraction buffers were supplemented with protease inhibitors (Roche, complete, Mini, EDTA-free) and 10 mM sodium fluoride and 1 mM sodium orthovanadate. Protein concentrations were determined using the BCA kit. For immunoblot analyses, the nuclear and cytoplasmic/membrane fractions were resolved by SDS-PAGE in two gels: 7.5% polyacrylamide for DDR1 and 4–20% polyacrylamide for glyceraldehyde 3-phosphate dehydrogenase (GAPDH) and Histone. After transfer, the first membrane was probed with an antibody recognizing phosphorylated DDR1 at Tyr513, namely DDR1 rabbit mAb E1N8F (Cat. # 14531) from Cell Signalling Technology (CST), Danvers, MA. After stripping, the membranes were re-probed with total anti-DDR1 (D1G6) rabbit mAb (Cat. # 5583, CST), which recognizes the C-terminal region of DDR1. The membrane was also reprobed for presence of transferrin receptor as a marker of membrane-anchored protein, using an anti-transferrin mouse mAb (Cat. # 612124) from BD Transduction Laboratories, San Jose, CA. The second membrane was probed with anti-Histone H1 mouse mAb (Cat. # 05-457, Sigma-Aldrich) and re-probed with anti-GAPDH mouse mAb (Cat. # MA5-15738, Thermo Fisher Scientific), as nuclear and cytoplasmic protein markers, respectively. Antigen/antibody complexes were visualized using the SuperSignal West Pico Plus and/or the SuperSignal West Femto Maximum Sensitivity Substrate from Thermo Fisher Scientific (Rockford, IL; Cat. # 34580 and 34095, respectively).
The primary objective was to evaluate the association between DDR1 IHC expression and GS, comparing between “low grade” (GS 3 + 4 or lower) and “high grade” (GS 4 + 3 or higher) tumors. For each PCa case, we summarized the quadruple core-level DDR1 data to patient-level data with overall staining percentage (OSP), a semi quantitative score defined as the percentage of positive stained cores among all quadruple cores, per tissue type (cancerous and adjacent normal), and per subcellular location (membrane, nuclear, or cytoplasm). TMA cores that had stroma, no glands, or no tissue after the staining process were considered as missing at random rather than negative staining.
Association between high/low grade GS and dichotomized DDR1 staining OSP (OSP = 0% vs OSP > 0%) was evaluated with Fisher’s exact test, per tissue type and sub-cellular location. To take into account the paired-tissue design of this TMA, we further evaluated DDR1 relative expression, which was categorized in three expression patterns: Equal expression (cancerous OSP = adjacent benign OSP), higher expression (cancerous OSP > adjacent benign OSP), and lower expression (cancerous OSP < adjacent benign OSP). The association between high/low grade GS and DDR1 relative expression patterns was then evaluated using Fisher’s exact test, per subcellular location.
The association between DDR1 and GS was further evaluated with multivariate logistic regression adjusted for tumor/node/metastasis (TNM) staging, classified as local (T0N0MX, T2N0MX, T2NXMX, and T2XN0MX) and advanced (T2XN1MX, T3AN0MX, T3AN1MX, T3ANXMX, T3BN0MX, and T3BN1MX) for each subcellular location. These evaluations were performed with DDR1’s OSP from cancer, OSP from normal, and relative DDR1 relative expression pattern (higher, equal, or lower expression), respectively.
For this cohort of TMA, we obtained de-identified baseline characteristics and clinical outcomes overall survival (OS), biochemical recurrence free survival (BCRFS), and cause-specific death. Associations between DDR1 expression and clinical outcomes such as OS and BCRFS were also performed with the Cox model. Competing risk analysis of cause-specific death was not performed as there were a very low event of death due to PCa in this cohort. All p values are 2-sided with a significance level of 0.05. The results should be regarded only as descriptive findings and multiple testing were not adjusted. All calculations were performed with statistical software R version 3.6.1.
Results and discussion
Using a TMA containing 1600 cores derived from radical prostatectomies from patients diagnosed with PCa, we examined the association between DDR1 expression through IHC and disease aggressiveness as defined by GS. The demographics and clinicopathologic features associated with the TMA cohort used for this study are shown in Table 1. Figure 1 shows representative IHC patterns detected by the Rab-819 antibody. Note the membranous (Fig. 1A) and nuclear (Fig. 1C) staining of DDR1. Because the Rab-819 antibody not only identified DDR1 at the cell membrane but also in the cytoplasm and/or the nucleus (Fig. 1B), we set to evaluate the tissue specimens for the subcellular distribution of DDR1 as a function of malignancy. For adjacent normal tissues there was no association between DDR1 expression and GS in any of the three subcellular locations examined (Fig. 2). In contrast, for cancer tissues, the fraction of cases that displayed membranous DDR1 expression was significantly lower in high GS tumors than in low GS tumors (Fig. 2A; p = 0.002). While these analyses suggest that DDR1 membranous expression decreases as tumors become more aggressive (high GS), this difference in membranous DDR1 staining between high and low GS cancerous areas did not translate into differences in nuclear or cytoplasmic DDR1 localization between low and high GS tumors (Fig. 2B, C; p = 0.71 and 0.16, respectively). Thus, the decrease in membranous DDR1 in more aggressive PCa tumors was not accompanied by a measurable change in DDR1 positivity in the other two subcellular locations, as indicated. Representative photographs of these results are shown in Fig. 3. Although DDR1 protein expression can be seen in the cell membrane of some benign glands (Fig. 3A, B), there is a trend towards enhanced membranous DDR1 expression in cancerous glands of lower GS cancers (Fig. 3C, D), which is less frequent in cancerous cells of higher GS tumors (Fig. 3E, F).
Membranous DDR1 expression in cancer vs. normal matched tissue is associated with low GS
Next, we compared membranous, cytoplasmic, and nuclear DDR1 expression in tumor tissues relative to that detected in corresponding adjacent normal tissues, in high and low GS tumors. As shown in Fig. 4A, these analyses revealed that the percentage of cases with low grade GS tumors with DDR1 immunoreactivity at the membrane was significantly higher than that observed in the high GS tumors (Fisher test, p = 0.007). In contrast, no significant differences in relative DDR1 expression at nuclear or cytoplasmic locations were found between low and high GS tumors (Fig. 4B, C). These data indicate that membranous expression of DDR1 is reduced in high GS tumors when compared to low GS tumors, and thus this subcellular location establishes an association between DDR1 and GS in PCa tumors. A previous study by Shimada et al. failed to find an association between DDR1 expression and GS in PCa . The reason for this discrepancy is likely to be due to the epitope recognized by the antibodies used for IHC. Shimada et al.  utilized an Ab to DDR1 raised against its C-terminal region (intracellular), whereas the Rab-819 antibody recognizes the extracellular domain of DDR1. The reason for the reduced immunoreactivity of DDR1 in the membrane of the high GS tumors reported here remains unknown. However, it could be due to posttranslational receptor regulation, which may include enhanced receptor endocytosis [43,44,45] and/or cleavage [46,47,48], all of which may decrease the levels of DDR1 at the cell surface and, consequently, Rab-819 Ab immunoreactivity. The differences in the levels of membranous DDR1 between low and high GS tumors may also be related to the levels of collagen IV in the basement membranes of the PCa tumors. It is well known that collagen IV is a major DDR1 ligand , and thus binding of collagen IV to DDR1 may play a role in mediating the interactions of prostate epithelial cells with their underlying basement membrane. Evidence has shown that in the course of PCa progression there is a marked loss of basement membrane and collagen IV [49, 50]. It is therefore tempting to speculate that the decreased expression of membranous DDR1 in high GS tumors represents a response to the loss of basement integrity as tumors become more aggressive.
DDR1 localizes in the nucleus of cultured prostate epithelial cells
Our IHC analyses revealed that a relatively higher DDR1 immunoreactivity was evident in the nuclei of PCa cells in high GS tumors than in those of low GS tumors (11 vs. 6%, respectively, Fig. 4B), suggesting that a subgroup of high GS tumors displays areas harboring cells with elevated nuclear DDR1 expression. Considering that DDR1 is a type I transmembrane protein, the presence of DDR1 in the nucleus is noteworthy. It is well established that several RTKs can translocate to the nucleus, where they can regulate gene expression [51, 52]. Importantly, a recent study by the Pozzi laboratory demonstrated that DDR1 can also be detected in the nucleus . Based on theirs results and our findings in the tissue specimens, we wished to examine whether DDR1 can be detected in the nuclear fraction of cultured human prostate epithelial cell lines. To this end, we first examined established prostate cell lines for expression of DDR1 in whole cell lysates under steady state conditions by immunoblot analyses. As shown in Fig. 5A, all non-malignant prostate cell lines (CF-91, MLC-8891, BPH-1, CRL-2221, RWPE-2 and RWPE-1) express DDR1 (~ 120 kDa). As for the human PCa cell lines studied herein (DU-145, PC-3, LNCaP and C4-2B), all express DDR1, except for DU145 cells. The lysates also contained a specific immunoreactive ~ 57-kDa protein representing proteolytically cleaved DDR1, which lacks the entire ectodomain and comprises a membrane-anchored C-terminal fragment (CTF) [47, 48]. Next, we examined the subcellular distribution (cytoplasmic/membrane, and nuclear) of DDR1 in untreated and collagen I-treated malignant PC-3 cells and immortalized non-malignant RWPE-1 prostate epithelial cells. As expected, total DDR1 receptor was detected in the cytoplasmic/membrane fractions, which was phosphorylated in response to collagen treatment in both cell lines (Fig. 5B, left panel). These analyses also revealed that total DDR1 could also be detected in the nuclear fraction of both PC-3 and RWPE-1 cells, with PC-3 cells showing relatively lower levels than RWPE-1 cells, under these conditions (Fig. 5B, right panel). Upon collagen stimulation, phosphorylated DDR1 was clearly detected in the nuclear fraction of both cell lines, with RWPE-1 cells showing relatively higher levels of nuclear phosphorylated DDR1. Because collagen is expected to bind and activate DDR1 at the cell surface, these results suggest that collagen-evoked receptor activation is followed by translocation of membrane-bound DDR1 to the nucleus. These results support the findings of nuclear DDR1 in our IHC studies and agree with the recent studies of Chiusa et al. . Collectively, these results add DDR1 to the list of RTK family members endowed with the ability to translocate to the nucleus [51, 52]. At present, the role of nuclear DDR1 in benign and cancerous prostate epithelial cells and its association with disease progression remain to be elucidated.
Membranous DDR1 as a predictor of aggressiveness and association with clinical outcome
The demographics and clinicopathologic features associated with the TMA cohort used for this study are shown in Table 1. We found that neither cytoplasmic nor nuclear DDR1 showed predictive value (data not shown) from our multivariate logistic regression analyses. However, while there was no significant association between DDR1 membranous expression and GS in adjacent normal tissue, consistent with the univariate analysis, DDR1 membranous expression in cancerous tissue is an independent predictor for tumor aggressiveness with statistically significant odds ratio of 0.97 (p = 0.001) (Table 2). For each 1% increase of OSP, the odds of having high GS are lowered 3%. Thus, the difference in DDR1 membranous expression in cancerous vs. adjacent benign tissue is an independent predictor of tumor aggressiveness. Because the event of OS or BCRFS were low in this cohort, only the results from the univariate Cox model analysis for OS or BCRFS are shown (Additional file 2: Table S2). Whereas traditional predictors, such as age, TNM, and Gleason scores, are significant predictors of OS and BCRFS, DDR1 expression is not.
In summary, this study evaluated the expression of DDR1 in a large cohort of PCa samples by IHC. We focused our analyses in evaluating DDR1 at various subcellular localizations that display positive immunoreactivity, which clearly identified DDR1 in the plasma membrane, the cytoplasm, and the nucleus. Thus, in this regard, this study is the first to evaluate the association between DDR1 subcellular localization and GS in PCa samples. Our data suggest that membrane, but not cytoplasmic or nuclear, localization of DDR1 better reflects the aggressiveness of PCa as defined by GS. We found that reduced positivity of DDR1 at the plasma membrane defines tumor lesions with high GS. Conversely, low GS cancers are characterized by higher levels of DDR1 at the plasma membrane. Therefore, our study highlights the notion that associations between cancer malignancy and DDR1 expression at least in PCa may need to address receptor subcellular location. Thus, based on our observations on DDR1 distribution, we surmise that membranous DDR1 is likely to play a role in the early stages of PCa development by mediating the interactions with the ECM. Consistent with the importance of DDR1-matrix interactions, our data showed that, overall, membranous DDR1 localization was a strong predictor of PCa aggressiveness. Finally, we showed that DDR1 is present in the nuclear compartment of PCa cells both in tissues and in cultured cell lines, reflecting a potential role for DDR1 in tumor cell behavior through receptor activity within the nuclear environment. More studies are warranted to define the mechanisms that regulate DDR1 traffic to the nucleus and its role in PCa progression.
Availability of data and materials
All the data used to support the findings of this study are included within the article and its supplementary information files. Please contact author for data requests.
American Type Culture Collection
Biochemical recurrence free survival
Benign prostatic hyperplasia
Discoidin Domain Receptor
Fetal bovine serum
Glyceraldehyde 3-phosphate dehydrogenase
Overall staining percentage
Prostate Cancer Biorepository Network
Receptor tyrosine kinase
Wayne State University
Leitinger B. Discoidin domain receptor functions in physiological and pathological conditions. Int Rev Cell Mol Biol. 2014;310:39–87.
Fu HL, Valiathan RR, Arkwright R, Sohail A, Mihai C, Kumarasiri M, et al. Discoidin domain receptors: unique receptor tyrosine kinases in collagen-mediated signaling. J Biol Chem. 2013;288:7430–7.
Lemeer S, Bluwstein A, Wu Z, Leberfinger J, Muller K, Kramer K, et al. Phosphotyrosine mediated protein interactions of the discoidin domain receptor 1. J Proteomics. 2012;75:3465–77.
Iwai LK, Luczynski MT, Huang PH. Discoidin domain receptors: a proteomic portrait. Cell Mol Life Sci. 2014;71:3269–79.
Borza CM, Pozzi A. Discoidin domain receptors in disease. Matrix Biol. 2014;34:185–92.
Carafoli F, Hohenester E. Collagen recognition and transmembrane signalling by discoidin domain receptors. Biochim Biophys Acta. 2013;1834:2187–94.
Leitinger B. Transmembrane collagen receptors. Annu Rev Cell Dev Biol. 2011;27:265–90.
Henriet E, Sala M, Abou Hammoud A, Tuariihionoa A, Di Martino J, Ros M, et al. Multitasking discoidin domain receptors are involved in several and specific hallmarks of cancer. Cell Adh Migr. 2018;12:363–77.
Gao Y, Zhou J, Li J. Discoidin domain receptors orchestrate cancer progression: a focus on cancer therapies. Cancer Sci. 2021;112:962–9.
Valiathan RR, Marco M, Leitinger B, Kleer CG, Fridman R. Discoidin domain receptor tyrosine kinases: new players in cancer progression. Cancer Metastasis Rev. 2012;31:295–321.
Rammal H, Saby C, Magnien K, Van-Gulick L, Garnotel R, Buache E, et al. Discoidin domain receptors: potential actors and targets in cancer. Front Pharmacol. 2016;7:55.
Payne LS, Huang PH. Discoidin domain receptor 2 signaling networks and therapy in lung cancer. J Thorac Oncol. 2014;9:900–4.
Jing H, Song J, Zheng J. Discoidin domain receptor 1: new star in cancer-targeted therapy and its complex role in breast carcinoma. Oncol Lett. 2018;15:3403–8.
Itoh Y. Discoidin domain receptors: microenvironment sensors that promote cellular migration and invasion. Cell Adh Migr. 2018;12:378–85.
Corsa CA, Brenot A, Grither WR, Van Hove S, Loza AJ, Zhang K, et al. The action of Discoidin domain receptor 2 in basal tumor cells and stromal cancer-associated fibroblasts is critical for breast cancer metastasis. Cell Rep. 2016;15:2510–23.
Ren T, Zhang W, Liu X, Zhao H, Zhang J, Zhang J, et al. Discoidin domain receptor 2 (DDR2) promotes breast cancer cell metastasis and the mechanism implicates epithelial-mesenchymal transition programme under hypoxia. J Pathol. 2014;234:526–37.
Jin H, Ham IH, Oh HJ, Bae CA, Lee DK, Kim YB, et al. Inhibition of discoidin domain receptor 1 prevents stroma-induced peritoneal metastasis in gastric carcinoma. Mol Cancer Res. 2018;16:1590–600.
Gao H, Chakraborty G, Zhang Z, Akalay I, Gadiya M, Gao Y, et al. Multi-organ site metastatic reactivation mediated by non-canonical discoidin domain receptor 1 signaling. Cell. 2016;166:47–62.
Rudra-Ganguly N, Lowe C, Mattie M, Chang MS, Satpayev D, Verlinsky A, et al. Discoidin domain receptor 1 contributes to tumorigenesis through modulation of TGFBI expression. PLoS ONE. 2014;9:e111515.
Sun X, Gupta K, Wu B, Zhang D, Yuan B, Zhang X, et al. Tumor-extrinsic discoidin domain receptor 1 promotes mammary tumor growth by regulating adipose stromal interleukin 6 production in mice. J Biol Chem. 2018;293:2841–9.
Yuge R, Kitadai Y, Takigawa H, Naito T, Oue N, Yasui W, et al. Silencing of Discoidin Domain Receptor-1 (DDR1) concurrently inhibits multiple steps of metastasis cascade in gastric cancer. Transl Oncol. 2018;11:575–84.
Ambrogio C, Gomez-Lopez G, Falcone M, Vidal A, Nadal E, Crosetto N, et al. Combined inhibition of DDR1 and Notch signaling is a therapeutic strategy for KRAS-driven lung adenocarcinoma. Nat Med. 2016;22:270–7.
Aguilera KY, Huang H, Du W, Hagopian MM, Wang Z, Hinz S, et al. Inhibition of Discoidin Domain receptor 1 reduces collagen-mediated tumorigenicity in pancreatic ductal adenocarcinoma. Mol Cancer Ther. 2017;16:2473–85.
Li Y, Lu X, Ren X, Ding K. Small molecule discoidin domain receptor kinase inhibitors and potential medical applications. J Med Chem. 2015;58:3287–301.
Liu L, Hussain M, Luo J, Duan A, Chen C, Tu Z, et al. Synthesis and biological evaluation of novel dasatinib analogues as potent DDR1 and DDR2 kinase inhibitors. Chem Biol Drug Des. 2017;89:420–7.
Murray CW, Berdini V, Buck IM, Carr ME, Cleasby A, Coyle JE, et al. Fragment-based discovery of potent and selective DDR1/2 inhibitors. ACS Med Chem Lett. 2015;6:798–803.
Siegel RL, Miller KD, Fuchs HE, Jemal A. Cancer statistics, 2021. CA Cancer J Clin. 2021;71:7–33.
Roehl KA, Han M, Ramos CG, Antenor JA, Catalona WJ. Cancer progression and survival rates following anatomical radical retropubic prostatectomy in 3,478 consecutive patients: long-term results. J Urol. 2004;172:910–4.
Freedland SJ, Humphreys EB, Mangold LA, Eisenberger M, Dorey FJ, Walsh PC, et al. Risk of prostate cancer-specific mortality following biochemical recurrence after radical prostatectomy. JAMA. 2005;294:433–9.
Kupelian PA, Mahadevan A, Reddy CA, Reuther AM, Klein EA. Use of different definitions of biochemical failure after external beam radiotherapy changes conclusions about relative treatment efficacy for localized prostate cancer. Urology. 2006;68:593–8.
Simmons MN, Stephenson AJ, Klein EA. Natural history of biochemical recurrence after radical prostatectomy: risk assessment for secondary therapy. Eur Urol. 2007;51:1175–84.
Jhaveri FM, Zippe CD, Klein EA, Kupelian PA. Biochemical failure does not predict overall survival after radical prostatectomy for localized prostate cancer: 10-year results. Urology. 1999;54:884–90.
D’Amico AV, Whittington R, Malkowicz SB, Fondurulia J, Chen MH, Tomaszewski JE, et al. The combination of preoperative prostate specific antigen and postoperative pathological findings to predict prostate specific antigen outcome in clinically localized prostate cancer. J Urol. 1998;160:2096–101.
Amin A, Partin A, Epstein JI. Gleason score 7 prostate cancer on needle biopsy: relation of primary pattern 3 or 4 to pathological stage and progression after radical prostatectomy. J Urol. 2011;186:1286–90.
Makarov DV, Sanderson H, Partin AW, Epstein JI. Gleason score 7 prostate cancer on needle biopsy: is the prognostic difference in Gleason scores 4 + 3 and 3 + 4 independent of the number of involved cores? J Urol. 2002;167:2440–2.
Chan TY, Partin AW, Walsh PC, Epstein JI. Prognostic significance of Gleason score 3+4 versus Gleason score 4+3 tumor at radical prostatectomy. Urology. 2000;56(5):823–7.
Magi-Galluzzi C, Montironi R, Epstein JI. Contemporary Gleason grading and novel Grade Groups in clinical practice. Curr Opin Urol. 2016;26:488–92.
Epstein JI, Egevad L, Amin MB, Delahunt B, Srigley JR, Humphrey PA, et al. The 2014 International Society of Urological Pathology (ISUP) consensus conference on gleason grading of prostatic carcinoma: definition of grading patterns and proposal for a new grading system. Am J Surg Pathol. 2016;40:244–52.
Shimada K, Nakamura M, Ishida E, Higuchi T, Yamamoto H, Tsujikawa K, et al. Prostate cancer antigen-1 contributes to cell survival and invasion though discoidin receptor 1 in human prostate cancer. Cancer Sci. 2008;99:39–45.
Azemikhah M, Ashtiani HA, Aghaei M, Rastegar H. Evaluation of discoidin domain receptor-2 (DDR2) expression level in normal, benign, and malignant human prostate tissues. Res Pharm Sci. 2015;10:356–63.
Moll S, Yasui Y, Abed A, Murata T, Shimada H, Maeda A, et al. Selective pharmacological inhibition of DDR1 prevents experimentally-induced glomerulonephritis in prevention and therapeutic regime. J Transl Med. 2018;16:148.
Richter H, Satz AL, Bedoucha M, Buettelmann B, Petersen AC, Harmeier A, et al. DNA-encoded library-derived DDR1 inhibitor prevents fibrosis and renal function loss in a genetic mouse model of alport syndrome. ACS Chem Biol. 2019;14:37–49.
Fu HL, Valiathan RR, Payne L, Kumarasiri M, Mahasenan KV, Mobashery S, et al. Glycosylation at Asn211 regulates the activation state of the discoidin domain receptor 1 (DDR1). J Biol Chem. 2014;289:9275–87.
Yeung DA, Shanker N, Sohail A, Weiss BA, Wang C, Wellmerling J, et al. Clustering, spatial distribution, and phosphorylation of discoidin domain receptors 1 and 2 in response to soluble collagen I. J Mol Biol. 2019;431:368–90.
Mihai C, Chotani M, Elton TS, Agarwal G. Mapping of DDR1 distribution and oligomerization on the cell surface by FRET microscopy. J Mol Biol. 2009;385:432–45.
Johnson N, Brezinova J, Stephens E, Burbridge E, Freeman M, Adrain C, et al. Quantitative proteomics screen identifies a substrate repertoire of rhomboid protease RHBDL2 in human cells and implicates it in epithelial homeostasis. Sci Rep. 2017;7:7283.
Shitomi Y, Thogersen IB, Ito N, Leitinger B, Enghild JJ, Itoh Y. ADAM10 controls collagen signaling and cell migration on collagen by shedding the ectodomain of discoidin domain receptor 1 (DDR1). Mol Biol Cell. 2015;26:659–73.
Fu HL, Sohail A, Valiathan RR, Wasinski BD, Kumarasiri M, Mahasenan KV, et al. Shedding of discoidin domain receptor 1 by membrane-type matrix metalloproteinases. J Biol Chem. 2013;288:12114–29.
Sinha AA, Gleason DF, DeLeon OF, Wilson MJ, Limas C, Reddy PK, et al. Localization of type IV collagen in the basement membranes of human prostate and lymph nodes by immunoperoxidase and immunoalkaline phosphatase. Prostate. 1991;18:93–104.
Fuchs ME, Brawer MK, Rennels MA, Nagle RB. The relationship of basement membrane to histologic grade of human prostatic carcinoma. Mod Pathol. 1989;2:105–11.
Carpenter G, Liao HJ. Receptor tyrosine kinases in the nucleus. Cold Spring Harb Perspect Biol. 2013;5:a008979.
Chen MK, Hung MC. Proteolytic cleavage, trafficking, and functions of nuclear receptor tyrosine kinases. FEBS J. 2015;282:3693–721.
Chiusa M, Hu W, Liao HJ, Su Y, Borza CM, de Caestecker MP, et al. The extracellular matrix receptor discoidin domain receptor 1 regulates collagen transcription by translocating to the nucleus. J Am Soc Nephrol. 2019;30:1605–24.
The authors particularly thank the patients, whose biospecimens were analyzed in this study.
This work was supported by the Department of Defense Prostate Cancer Research Program, DOD Award No W81XWH-15-1-0226 (to RF and RDB) and Awards No W81XWH-10-2-0056 and W81XWH-10-2-0046 Prostate Cancer Biorepository Network (PCBN).
Ethics approval and consent to participate
This study is covered under Institutional Review Board (IRB) approval of Wayne State University (IRB# 092014MP2X), and Johns Hopkins University (IRB # NA-00048544).
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The authors declare no competing interests.
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Bonfil, R.D., Chen, W., Vranic, S. et al. Expression and subcellular localization of Discoidin Domain Receptor 1 (DDR1) define prostate cancer aggressiveness. Cancer Cell Int 21, 507 (2021). https://doi.org/10.1186/s12935-021-02206-1
- Prostate cancer
- Receptor tyrosine kinases
- Prognostic markers