ROBO1 protein expression is independently associated with biochemical recurrence in prostate cancer patients who underwent radical prostatectomy in Asian patients

前列腺切除术 前列腺癌 生化复发 医学 比例危险模型 危险系数 生存分析 免疫组织化学 基因敲除 癌症 肿瘤科 前列腺 癌症研究 泌尿科 内科学 病理 生物 细胞培养 遗传学 置信区间
作者
Sang Hoon Kim,Taejung Kim,Dong-Ho Shin,Kyung Jae Hur,Sung-Hoo Hong,Ji Youl Lee,U-Syn Ha
出处
期刊:Gland surgery [AME Publishing Company]
被引量:1
标识
DOI:10.21037/gs-21-406
摘要

The purpose of this study is to investigate the correlation between ROBO1 expression and prostate cancer aggressiveness.ROBO1 expression was evaluated in normal prostate epithelial cells (PrEC) and different prostate cancer cell lines by Western blot analysis. The migration and invasion of native and ROBO1 knockdown cells were evaluated using migration chambers and a Matrigel-coated membrane, respectively. Samples from 145 patients who underwent radical prostatectomy between June 2000 and June 2008, were retrieved from the paraffin files for tissue microarray (TMA) with immunohistochemical analysis. Biochemical recurrence (BCR)-free survival curves were estimated using the Kaplan-Meier and Cox regression methods in two groups of patients classified according to the degree of ROBO1 expression (low or high expression).ROBO1 is highly expressed in the prostate cancer cell lines. All ROBO1 knockdown cells (PC3, 22Rv1 and DU 145) showed markedly decreased migration and invasiveness compared to native cells. In 145 patients with radical prostatectomy, the Kaplan-Meier curves and log-rank test for BCR-free survival stratified by ROBO1 expression in organ-confined (pT2) or not (pT3), showed significant differences in 10-year survival between the ROBO1 high and low expression groups (87.2% versus 52.6% in pT2; P=0.047, 51.0% versus 36.9% in pT3; P=0.033). The multivariable-adjusted model showed a markedly increased hazard ratio (HR) in patients with high ROBO1 expression compared to the patients with low ROBO1expression in every model.ROBO1 may play an important role in the migration and invasion of prostate cancer cells, and was independently associated with BCR.

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