Skip to main content

Table 9 Dysregulation of CDK3 in clinical samples

From: A review on the role of cyclin dependent kinases in cancers

Tumor type

Samples

Expression

(Tumor vs. Normal)

Kaplan–Meier analysis (impact of regulators dysregulation)

Multivariate Cox regression analysis

Association of dysregulation of regulators with clinicopathologic characteristics

References

Breast cancer

37 cases of lymph node metastatic BC tissues, and 28 cases of lymph node non-metastatic BC tissues

194 cases of BC tissues and 59 cases of normal tissues

Up-regulation of CDK3 in primary tumor tissues

_

_

_

[181]

30 PTANCT

Up-regulation of HuR and CDK3

_

_

chemoresistance

[187]

37 PTANCT

Up-regulation of CDK3 and down of miR-125a-3p

_

_

_

[183]

Colorectal cancer

87 cases of PCC, 49 cases of MCC, and 52 cases of normal colon tissues

Up-regulation of CDK3 in MCC than PCC and in PCC than normal

_

_

TNM grade

[185]

50 PTANCT

Up-regulation of circRNA_141539 (which regulated CDK3)

Shorter PFS

High levels of circRNA_141539 and low differentiation and stage III were found to be poor survival prognostic factors

TNM stage, T stage, and N stage, and negatively with histological grade

[186]

Hepatocellular carcinoma

GEO database (GSE22058: 96 PTANCT)

8 PTANCT

Down-regulation of miR-214/199a/199a* (which regulated CDK3)

Shorter OS

miR-214 expression was found to be an independent prognostic factor

_

[189]

Lung cancer

31 PTANCT

Up-regulation of HuR (which regulated CDK3)

_

_

_

[191]

Nasopharyngeal carcinoma

94 NPC tissues and 40 inflamed nasopharyngeal tissues

Up-regulation of CDK3 in NPC

_

_

infiltration, lymph node metastasis, tumor node metastasis, and TNM clinical staging

[192]

Skin cancer

65 tumor tissues and 9 normal tissues

Up-regulation of NFAT3

_

_

CDK3 levels were positively associated with both NFAT3 and phosphorylated NFAT3-Ser259

[193]

  1. PCC primary colon cancer, MCC metastatic colon cancer, TNM tumor node metastasis, PTANC pairs of tumor samples and adjacent non-cancerous samples, NPC Nasopharyngeal carcinoma, PFS progression-free survival