mTORC2 Regulates Amino Acid Metabolism in Cancer by Phosphorylation of the Cystine-Glutamate Antiporter xCT

作者：Gu Yuchao; Albuquerque Claudio P; Braas Daniel; Zhang Wei; Villa Genaro R; Bi Junfeng; Ikegami Shiro; Masui Kenta; Gini Beatrice; Yang Huijun; Gahman Timothy C; Shiau Andrew K; Cloughesy Timothy F; Christofk Heather R; Zhou Huilin; Guan Kun Liang; Mischel Paul S^*

来源：Molecular Cell, 2017, 67(1): 128-+.

DOI：10.1016/j.molcel.2017.05.030

Mutations in cancer reprogram amino acid metabolism to drive tumor growth, but the molecular mechanisms are not well understood. Using an unbiased proteomic screen, we identified mTORC2 as a critical regulator of amino acid metabolism in cancer via phosphorylation of the cystine-glutamate antiporter xCT. mTORC2 phosphorylates serine 26 at the cytosolic N terminus of xCT, inhibiting its activity. Genetic inhibition of mTORC2, or pharmacologic inhibition of the mammalian target of rapamycin (mTOR) kinase, promotes glutamate secretion, cystine uptake, and incorporation into glutathione, linking growth factor receptor signaling with amino acid uptake and utilization. These results identify an unanticipated mechanism regulating amino acid metabolism in cancer, enabling tumor cells to adapt to changing environmental conditions.

• 出版日期2017-7-6