Literature DB >> 23906303

The predictive value of semaphorins 3 expression in biopsies for biochemical recurrence of patients with low- and intermediate-risk prostate cancer.

K Li, M K Chen, L Y Li, M H Lu, Ch K Shao, Z L Su, D He, J Pang, X Gao.   

Abstract

The class-3 semaphorins (Sema3A-F, Sema3s) are initially identified to play an important role in axonal guidance and cell migration. Our previous studies showed that Sema3s are also involved in the lymph node metastasis of prostate cancer, and are likely to modulate the behavior of prostate cancer with a pro-tumoral or an anti-tumoral effect, depending on their subtypes. However, no study has critically investigated the value of Sema3s expression in preoperative biopsy samples for the prediction of biochemical recurrence (BCR) after radical prostatectomy. In this study, we evaluated Sema3s expression by immunohistochemistry on 198 prostate biopsies with low- and intermediate-risk localized prostate cancer. The median follow-up was 42 months (range, 6-60) for all patients. Our results showed that Sema3A (OR: 0.19, P<0.001), Sema3B (OR: 0.38, P=0.003), Sema3E (OR: 0.39, P=0.007), and Sema3C (OR: 2.31, P=0.014) staining were independent predictors of BCR on multivariable analysis. Sema3A, 3B, 3C and 3E expression demonstrated potential values in predicting BCR upon survival analysis (P=0.001, P=0.003, P=0.029, P=0.037, respectively, Log-rank test). Our findings suggested that Sema3A, 3B, 3C, and 3E immunostaining in prostate biopsies, as supplements to clinicopathological parameters, could be used for predicting BCR in low- and intermediate-risk prostate cancer patients after radical prostatectomy. Specially, concurrent Sema3C-positive and Sema3A-negative, 3B-negative, 3E-negative staining is associated with an adverse prognosis. Further prospective studies in larger patient populations are needed to validate the current observations.

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Year:  2013        PMID: 23906303     DOI: 10.4149/neo_2013_087

Source DB:  PubMed          Journal:  Neoplasma        ISSN: 0028-2685            Impact factor:   2.575


  10 in total

1.  TET1-mediated different transcriptional regulation in prostate cancer.

Authors:  Jianhua Feng; Qiang Wang; Guangwei Li; Xiangjian Zeng; Shihang Kuang; Xiaohua Li; Youwei Yue
Journal:  Int J Clin Exp Med       Date:  2015-01-15

2.  Tumor Suppressor Function of the SEMA3B Gene in Human Lung and Renal Cancers.

Authors:  Vitaly I Loginov; Alexey A Dmitriev; Vera N Senchenko; Irina V Pronina; Dmitry S Khodyrev; Anna V Kudryavtseva; George S Krasnov; Ganna V Gerashchenko; Larisa I Chashchina; Tatiana P Kazubskaya; Tatiana T Kondratieva; Michael I Lerman; Debora Angeloni; Eleonora A Braga; Vladimir I Kashuba
Journal:  PLoS One       Date:  2015-05-11       Impact factor: 3.240

3.  Androgen receptor transcriptionally regulates semaphorin 3C in a GATA2-dependent manner.

Authors:  Kevin J Tam; Kush Dalal; Michael Hsing; Chi Wing Cheng; Shahram Khosravi; Parvin Yenki; Charan Tse; James W Peacock; Aishwariya Sharma; Yan Ting Chiang; Yuzhuo Wang; Artem Cherkasov; Paul S Rennie; Martin E Gleave; Christopher J Ong
Journal:  Oncotarget       Date:  2017-02-07

4.  The X-linked tumor suppressor TSPX downregulates cancer-drivers/oncogenes in prostate cancer in a C-terminal acidic domain dependent manner.

Authors:  Tatsuo Kido; Yunmin Li; Yuichiro Tanaka; Rajvir Dahiya; Yun-Fai Chris Lau
Journal:  Oncotarget       Date:  2019-02-19

Review 5.  The emerging role of class-3 semaphorins and their neuropilin receptors in oncology.

Authors:  Patrick Nasarre; Robert M Gemmill; Harry A Drabkin
Journal:  Onco Targets Ther       Date:  2014-09-24       Impact factor: 4.147

6.  The evaluative value of Sema3C and MFN2 co-expression detected by immunohistochemistry for prognosis in hepatocellular carcinoma patients after hepatectomy.

Authors:  Xu Feng; Kelei Zhu; Jinghua Liu; Jiang Chen; Jiacheng Tang; Yuelong Liang; Renan Jin; Xiao Liang; Xiujun Cai
Journal:  Onco Targets Ther       Date:  2016-05-30       Impact factor: 4.147

7.  Semaphorin 3 C drives epithelial-to-mesenchymal transition, invasiveness, and stem-like characteristics in prostate cells.

Authors:  Kevin J Tam; Daniel H F Hui; Wilson W Lee; Mingshu Dong; Tabitha Tombe; Ivy Z F Jiao; Shahram Khosravi; Ario Takeuchi; James W Peacock; Larissa Ivanova; Igor Moskalev; Martin E Gleave; Ralph Buttyan; Michael E Cox; Christopher J Ong
Journal:  Sci Rep       Date:  2017-09-13       Impact factor: 4.379

8.  SEMA3C drives cancer growth by transactivating multiple receptor tyrosine kinases via Plexin B1.

Authors:  James W Peacock; Ario Takeuchi; Norihiro Hayashi; Liangliang Liu; Kevin J Tam; Nader Al Nakouzi; Nastaran Khazamipour; Tabitha Tombe; Takashi Dejima; Kevin Ck Lee; Masaki Shiota; Daksh Thaper; Wilson Cw Lee; Daniel Hf Hui; Hidetoshi Kuruma; Larissa Ivanova; Parvin Yenki; Ivy Zf Jiao; Shahram Khosravi; Alice L-F Mui; Ladan Fazli; Amina Zoubeidi; Mads Daugaard; Martin E Gleave; Christopher J Ong
Journal:  EMBO Mol Med       Date:  2018-02       Impact factor: 12.137

Review 9.  Semaphorin 3C and Its Receptors in Cancer and Cancer Stem-Like Cells.

Authors:  Jing Hao; Jennifer S Yu
Journal:  Biomedicines       Date:  2018-04-08

10.  PlexinB1 Promotes Nuclear Translocation of the Glucocorticoid Receptor.

Authors:  Magali Williamson; Ritu Garg; Claire M Wells
Journal:  Cells       Date:  2019-12-18       Impact factor: 6.600

  10 in total

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