The cell cycle regulator 14-3-3σ opposes and reverses cancer metabolic reprogramming

细胞周期调节因子14-3-3σ 抑制并逆转癌症代谢重编程

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作者:Liem Phan ,Ping-Chieh Chou ,Guermarie Velazquez-Torres ,Ismael Samudio ,Kenneth Parreno ,Yaling Huang ,Chieh Tseng ,Thuy Vu ,Chris Gully ,Chun-Hui Su ,Edward Wang ,Jian Chen ,Hyun-Ho Choi ,Enrique Fuentes-Mattei ,Ji-Hyun Shin ,Christine Shiang ,Brian Grabiner ,Marzenna Blonska ,Stephen Skerl ,Yiping Shao ,Dianna Cody ,Jorge Delacerda ,Charles Kingsley ,Douglas Webb ,Colin Carlock ,Zhongguo Zhou ,Yun-Chih Hsieh ,Jaehyuk Lee ,Andrew Elliott ,Marc Ramirez ,Jim Bankson ,John Hazle ,Yongxing Wang ,Lei Li ,Shaofan Weng ,Nibal Rizk ,Yu Ye Wen ,Xin Lin ,Hua Wang ,Huamin Wang ,Aijun Zhang ,Xuefeng Xia ,Yun Wu ,Mouhammed Habra ,Wei Yang ,Lajos Pusztai ,Sai-Ching Yeung ,Mong-Hong Lee

Abstract

Extensive reprogramming of cellular energy metabolism is a hallmark of cancer. Despite its importance, the molecular mechanism controlling this tumour metabolic shift remains not fully understood. Here we show that 14-3-3σ regulates cancer metabolic reprogramming and protects cells from tumorigenic transformation. 14-3-3σ opposes tumour-promoting metabolic programmes by enhancing c-Myc poly-ubiquitination and subsequent degradation. 14-3-3σ demonstrates the suppressive impact on cancer glycolysis, glutaminolysis, mitochondrial biogenesis and other major metabolic processes of tumours. Importantly, 14-3-3σ expression levels predict overall and recurrence-free survival rates, tumour glucose uptake and metabolic gene expression in breast cancer patients. Thus, these results highlight that 14-3-3σ is an important regulator of tumour metabolism, and loss of 14-3-3σ expression is critical for cancer metabolic reprogramming. We anticipate that pharmacologically elevating the function of 14-3-3σ in tumours could be a promising direction for targeted anticancer metabolism therapy development in future.

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