Chen Jian, Lu Huijun, Yan Dongwang, Cui Feifei, Wang Xiaoliang, Yu Fudong, Xue Yingming, Feng Xiaodong, Wang Jingtao, Wang Xiao, Jiang Tao, Zhang Meng, Zhao Senlin, Yu Yang, Tang Huamei, Peng Zhihai
Department of General Surgery, Shanghai First People's Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, People's Republic of China.
Department of Pathology, Shanghai First People's Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, People's Republic of China.
Oncotarget. 2015 Jan 1;6(1):355-67. doi: 10.18632/oncotarget.2803.
p21-Activated kinase 6 (PAK6) has been implicated in radiotherapy and docetaxel resistance. We have further evaluated PAK6 as a predictor of 5-fluorouracil (5-FU) treatment response in colon cancer. Here we report that in colon cancer PAK6 promotes tumor progression and chemoresistance both in vitro and in vivo. In the clinical analysis, PAK6 was overexpressed in 104 of 147 (70.75%) stage II and III patients who received 5-FU based chemotherapy after surgery. Multivariate Cox regression analysis indicated that PAK6 was an independent prognostic factor for overall survival (P < 0.001) and disease-free survival (P < 0.001). Colon cancer cell lines showed increased PAK6 expression upon 5-FU treatment. In PAK6-knockdown cells treated with 5-FU, cell viability and phosphorylation of BAD decreased, and the number of apoptotic cells, levels of cleaved caspase 3 and PARP increased compared to control cells. The opposite was observed in PAK6 overexpressing cells. Short hairpin RNA knockdown of PAK6 blocked cells in G2-M phase. Furthermore, Animal experiments results in vivo are consistent with outcomes in vitro. This study demonstrates that PAK6 is an independent prognostic factor for adjuvant 5-FU-based chemotherapy in patients with stage II and stage III colon cancer.
p21激活激酶6(PAK6)与放疗和多西他赛耐药有关。我们进一步评估了PAK6作为结肠癌中5-氟尿嘧啶(5-FU)治疗反应预测指标的作用。在此我们报告,在结肠癌中,PAK6在体外和体内均促进肿瘤进展和化疗耐药。在临床分析中,147例接受术后基于5-FU化疗的II期和III期患者中有104例(70.75%)PAK6过表达。多变量Cox回归分析表明,PAK6是总生存期(P < 0.001)和无病生存期(P < 0.001)的独立预后因素。5-FU处理后,结肠癌细胞系PAK6表达增加。与对照细胞相比,用5-FU处理的PAK6敲低细胞中,细胞活力和BAD磷酸化降低,凋亡细胞数量、裂解的caspase 3和PARP水平增加。在PAK6过表达细胞中观察到相反的情况。PAK6的短发夹RNA敲低使细胞阻滞在G2-M期。此外,体内动物实验结果与体外结果一致。本研究表明,PAK6是II期和III期结肠癌患者辅助性基于5-FU化疗的独立预后因素。