Cancer Lett 2011 Dec;312 (1): 55-61. [IF:4.864]
Disruption of xCT inhibits cell growth via the ROS/autophagy pathway in hepatocellular carcinoma.
Guo W , Zhao Y , Zhang Z , Tan N , Zhao F , Ge C , Liang L , Jia D , Chen T , Yao M , Li J , He X .
Shanghai Medical College, Fudan University, Shanghai 200032, China. guoweijie1986@hotmail.com
上海医学院，复旦大学
Abstract
xCT, the functional subunit of the system x(c)(-) which plays an important role in maintaining intracellular glutathione (GSH) levels, is expressed in various malignant tumors. Here, we demonstrated that xCT expression is often elevated in HCC and is associated with poor prognosis in HCC patients; moreover, disruption of xCT suppressed HCC cell growth both in vitro and in vivo. xCT dysfunction has also been shown to increase intracellular reactive oxygen species (ROS) levels, thus in turn led to autophagic cell death of HCC cells. Taken together, these findings suggest that xCT may be a promising therapeutic target for human HCC.
