Tumor Suppressor Role and Clinical Significance of the FEV Gene in Prostate Cancer

Author:

Liang Yu-Xiang12ORCID,Liang Ying-Ke12ORCID,Zou Zhi-Hao12ORCID,Zhuo Yang-Jia12ORCID,Ye Jian-Heng12ORCID,Zhu Xue-Jin12ORCID,Cai Zhou-Da12ORCID,Lin Zhuo-Yuan3ORCID,Mo Ru-Jun4ORCID,Wu Shu-Lin5,Zhang Yan-Qiong6ORCID,Zhong Wei-De12578ORCID

Affiliation:

1. Department of Urology, Guangdong Key Laboratory of Clinical Molecular Medicine and Diagnostics, Guangzhou First People’s Hospital, School of Medicine, South China University of Technology, Guangzhou 510180, China

2. Department of Urology, Guangdong Key Laboratory of Clinical Molecular Medicine and Diagnostics, Guangzhou First People’s Hospital, Guangzhou Medical University, Guangzhou 510180, China

3. Department of Urology, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou Medical University, Guangzhou 510260, China

4. Department of Urology, Affiliated Dongguan Hospital, Southern Medicine University, Dongguan 523059, China

5. Departments of Urology and Pathology, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA

6. Institute of Chinese Materia Medical, China Academy of Chinese Medical Sciences, Beijing 100700, China

7. Department of Urology, Huadu District People's Hospital, Southern Medical University, Guangzhou 510800, China

8. School of Medicine, Jinan University, Guangzhou, Guangdong 510632, China

Abstract

Background. In our previous research, we developed a 32-gene risk index model that may be utilized as a robust prognostic method for predicting prostate cancer (PCa) recurrence after surgery. Among the 32 genes, the Fifth Ewing Variant (FEV) gene was one of the top downregulated genes in relapsed PCa. However, current understanding of the FEV gene and its involvement in PCa is limited. Methods. FEV mRNA expression was analyzed and correlated to clinical outcomes in PCa patients who underwent prostatectomy at the Massachusetts General Hospital. Specimens from tissue microarray (TMA) including 102 prostate cancer patients were analysis for the expression of FEV. Meanwhile, FEV expression profiles were also assessed in PCa cell lines and in BPH-1 prostate epithelial cells using western blotting and quantitative reverse transcription-PCR (qRT-PCR). Furthermore, we transfected LNCaP and PC-3 cells with either an empty vector or full-length FEV gene and performed in vitro cell functional assays. The part FEV plays in tumor xenograft growth was also assessed in vivo. Results. Of the 191 patients included in this study base on the DASL dataset, 77 (40.3%) and 24 (13.6%), respectively, developed prostate-specific antigen (PSA) relapse and metastasis postradical prostatectomy. Significant FEV downregulation was observed in PCa patients showing PSA failure and metastasis. The protein expression of FEV was significantly negatively correlated with the Gleason score and pathological stage in prostate cancer tissues. Similarly, FEV expression significantly decreased in all PCa cell lines relative to BPH-1 (all P < 0.05 ). Functional assays revealed that FEV expression markedly inhibited PCa cell growth, migration, and invasion, which in turn significantly repressed the growth of tumor xenografts in vivo. Conclusion. The results of this study suggest an association between downregulated FEV expression and PSA relapse in PCa patients. In addition, FEV may act as a tumor suppressor in PCa.

Funder

Guangdong Basic and Applied Basic Research Foundation

Publisher

Hindawi Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics,Molecular Biology,General Medicine

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