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Article

Overexpression of ID1 promotes tumor progression in penile squamous cell carcinoma

  • Authors:
    • Xiheng Hu
    • Mingfeng Chen
    • Yangle Li
    • Yin Wang
    • Sailan Wen
    • Fu Jun
  • View Affiliations / Copyright

    Affiliations: Department of Urology, Xiangya Hospital, Central South University, Changsha, Human 410008, P.R. China, Department of Pathology, Xiangya Hospital, Central South University, Changsha, Human 410008, P.R. China, Department of Oncology, Xiangya Hospital, Central South University, Changsha, Human 410008, P.R. China
  • Pages: 1091-1100
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    Published online on: December 6, 2018
       https://doi.org/10.3892/or.2018.6912
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Abstract

Penile squamous cell carcinoma (PSCC) occurs more frequently in developing countries, and is commonly diagnosed at an advanced stage with an unfavorable prognosis. At present, few biomarkers for PSCC have been identified and used in clinical practice. Aberrant expression of inhibitor of DNA binding 1 (ID1) has been suggested as a potential regulator of tumor progression in various types cancer. Herein, we evaluated ID1 expression in PSCC and analyzed its association with the clinicopathological parameters of PSCC. Our findings indicated that ID1 overexpression is associated with histological subtype and lymph node metastasis. Kaplan‑Meier survival analysis showed that the overexpression of ID1 is associated with unfavorable cancer‑specific survival. In Cox proportional hazard models, ID1 overexpression was found to be an independent predictor of cancer‑specific survival. Furthermore, we investigated the function of ID1 in PSCC using a PSCC cell line Penl1. Silencing of ID1 expression retarded cell growth, inhibited clonogenesis, and attenuated cell migration and invasion in Penl1 cells. ID1 may regulate key oncogenic and metastasis‑related molecules, as depletion of ID1 expression affected the levels of p‑AKT, p16, PTEN and cleaved caspase‑3, and reduced MMP2/9 secretion in Penl1 cells. Nevertheless, the mRNA expression of p16 and PTEN increased following ID1 knockdown, suggesting that ID1 may repress p16 and PTEN expression in Penl1 cells. Therefore, overexpression of ID1 could serve as a potential prognostic biomarker for the clinical management of PSCC. Strategies targeting ID1‑regulated signaling pathways may have therapeutic benefit in PSCC.
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Copy and paste a formatted citation
Spandidos Publications style
Hu X, Chen M, Li Y, Wang Y, Wen S and Jun F: Overexpression of ID1 promotes tumor progression in penile squamous cell carcinoma. Oncol Rep 41: 1091-1100, 2019.
APA
Hu, X., Chen, M., Li, Y., Wang, Y., Wen, S., & Jun, F. (2019). Overexpression of ID1 promotes tumor progression in penile squamous cell carcinoma. Oncology Reports, 41, 1091-1100. https://doi.org/10.3892/or.2018.6912
MLA
Hu, X., Chen, M., Li, Y., Wang, Y., Wen, S., Jun, F."Overexpression of ID1 promotes tumor progression in penile squamous cell carcinoma". Oncology Reports 41.2 (2019): 1091-1100.
Chicago
Hu, X., Chen, M., Li, Y., Wang, Y., Wen, S., Jun, F."Overexpression of ID1 promotes tumor progression in penile squamous cell carcinoma". Oncology Reports 41, no. 2 (2019): 1091-1100. https://doi.org/10.3892/or.2018.6912
Copy and paste a formatted citation
x
Spandidos Publications style
Hu X, Chen M, Li Y, Wang Y, Wen S and Jun F: Overexpression of ID1 promotes tumor progression in penile squamous cell carcinoma. Oncol Rep 41: 1091-1100, 2019.
APA
Hu, X., Chen, M., Li, Y., Wang, Y., Wen, S., & Jun, F. (2019). Overexpression of ID1 promotes tumor progression in penile squamous cell carcinoma. Oncology Reports, 41, 1091-1100. https://doi.org/10.3892/or.2018.6912
MLA
Hu, X., Chen, M., Li, Y., Wang, Y., Wen, S., Jun, F."Overexpression of ID1 promotes tumor progression in penile squamous cell carcinoma". Oncology Reports 41.2 (2019): 1091-1100.
Chicago
Hu, X., Chen, M., Li, Y., Wang, Y., Wen, S., Jun, F."Overexpression of ID1 promotes tumor progression in penile squamous cell carcinoma". Oncology Reports 41, no. 2 (2019): 1091-1100. https://doi.org/10.3892/or.2018.6912
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