Li Wenzhi, Guo Fengfu, Gu Meng, Wang Guangjian, He Xiangfei, Zhou Juan, Peng Yubing, Wang Zhong, Wang Xiang
1. Department of Urology, Linyi People's Hospital Affiliated to Shandong University, Shandong, China ; 2. Department of Urology, Ninth People's Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China.
1. Department of Urology, Linyi People's Hospital Affiliated to Shandong University, Shandong, China.
J Cancer. 2015 Feb 27;6(5):420-9. doi: 10.7150/jca.11228. eCollection 2015.
Golgi phosphoprotein 3 (GOLPH3) is a metastasis-associated gene, however its role in cell proliferation of prostate cancer (PCa) has not yet been elucidated.
The level of expression of GOLPH3 and other genes was examined by quantitative real-time PCR (QPCR) and western blot analysis. Furthermore, we performed a comprehensive analysis of the expression of GOLPH3 in PCa using a tissue microarray (TMA) and correlated our findings with pathological parameters of PCa. RNA interference (RNAi) was used to silence the expression of GOLPH3 in PC-3 cells and to measure the effects on proliferation and cell cycle using the CCK-8 assay and flow cytometry. Western blots were also employed to assess AKT-mTOR and cell cycle-related proteins.
We showed that the expression of GOLPH3 was located at the trans-Golgi membranes in PCa cells. We found that GOLPH3 was expressed in all PCa cells and was significantly higher in two androgen-independent cell lines, DU145 and PC-3. TMA immunohistochemistry showed that GOLPH3 was positive in 64% of cancer tissue samples compared with 20% in normal and 30% in benign samples (P<0.05). In vitro, silencing GOLPH3 expression inhibited cell proliferation and arrested the cell cycle at the G2/M phase. Silencing GOLPH3 also activated P21 expression but suppressed the expression of CDK1/2 and cyclinB1 protein together with the phosphorylation of AKT and mTOR.
The expression of the GOLPH3 protein was significantly elevated in PCa. GOLPH3 can promote cell proliferation by enhancing the activity of AKT-mTOR signaling. Altogether, these findings suggest that GOLPH3 play important roles in proliferation and cell cycle regulation in PCa and might serve as promising biomarkers for PCa progression as well as potential therapeutic targets.
高尔基体磷蛋白3(GOLPH3)是一种与转移相关的基因,然而其在前列腺癌(PCa)细胞增殖中的作用尚未阐明。
通过定量实时PCR(QPCR)和蛋白质印迹分析检测GOLPH3及其他基因的表达水平。此外,我们使用组织微阵列(TMA)对PCa中GOLPH3的表达进行了全面分析,并将我们的研究结果与PCa的病理参数相关联。使用RNA干扰(RNAi)沉默PC-3细胞中GOLPH3的表达,并使用CCK-8法和流式细胞术测量对增殖和细胞周期的影响。还采用蛋白质印迹法评估AKT-mTOR和细胞周期相关蛋白。
我们发现GOLPH3的表达定位于PCa细胞的反式高尔基体膜上。我们发现GOLPH3在所有PCa细胞中均有表达,并且在两种雄激素非依赖性细胞系DU145和PC-3中显著更高。TMA免疫组织化学显示,64%的癌组织样本中GOLPH3呈阳性,而正常样本中为20%,良性样本中为30%(P<0.05)。在体外,沉默GOLPH3表达可抑制细胞增殖并使细胞周期停滞在G2/M期。沉默GOLPH3还激活了P21的表达,但抑制了CDK1/2和细胞周期蛋白B1蛋白的表达以及AKT和mTOR的磷酸化。
GOLPH3蛋白的表达在PCa中显著升高。GOLPH3可通过增强AKT-mTOR信号传导的活性来促进细胞增殖。总之,这些发现表明GOLPH3在PCa的增殖和细胞周期调控中起重要作用,并且可能作为PCa进展的有前景的生物标志物以及潜在的治疗靶点。