Kim Raymond H, Peters Malte, Jang YingJu, Shi Wei, Pintilie Melania, Fletcher Graham C, DeLuca Carmela, Liepa Jennifer, Zhou Lily, Snow Bryan, Binari Richard C, Manoukian Armen S, Bray Mark R, Liu Fei-Fei, Tsao Ming-Sound, Mak Tak W
Advanced Medical Discovery Institute, The Campbell Family Institute for Breast Cancer Research, Ontario Cancer Institute, Toronto, Canada M5G 2C1.
Cancer Cell. 2005 Mar;7(3):263-73. doi: 10.1016/j.ccr.2005.02.010.
The phosphatidylinositol 3' kinase (PI3'K) pathway, which regulates cell survival, is antagonized by the PTEN tumor suppressor. The regulation of PTEN is unclear. A genetic screen of Drosophila gain-of-function mutants identified DJ-1 as a suppressor of PTEN function. In mammalian cells, DJ-1 underexpression results in decreased phosphorylation of PKB/Akt, while DJ-1 overexpression leads to hyperphosphorylation of PKB/Akt and increased cell survival. In primary breast cancer samples, DJ-1 expression correlates negatively with PTEN immunoreactivity and positively with PKB/Akt hyperphosphorylation. In 19/23 primary non-small cell lung carcinoma samples, DJ-1 expression was increased compared to paired nonneoplastic lung tissue, and correlated positively with relapse incidence. DJ-1 is thus a key negative regulator of PTEN that may be a useful prognostic marker for cancer.
磷脂酰肌醇3'激酶(PI3'K)信号通路可调节细胞存活,该通路受到PTEN肿瘤抑制因子的拮抗作用。PTEN的调控机制尚不清楚。对果蝇功能获得性突变体进行的基因筛选确定DJ-1为PTEN功能的抑制因子。在哺乳动物细胞中,DJ-1表达不足导致蛋白激酶B(PKB)/Akt磷酸化水平降低,而DJ-1过表达则导致PKB/Akt过度磷酸化并增加细胞存活。在原发性乳腺癌样本中,DJ-1表达与PTEN免疫反应性呈负相关,与PKB/Akt过度磷酸化呈正相关。在23份原发性非小细胞肺癌样本中的19份中,与配对的非肿瘤性肺组织相比,DJ-1表达增加,且与复发率呈正相关。因此,DJ-1是PTEN的关键负调控因子,可能是一种有用的癌症预后标志物。