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

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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
机构
[1] The University of Texas MD Anderson Cancer Center,Department of Molecular and Cellular Oncology
[2] Graduate School of Biomedical Sciences,Department of Leukemia
[3] The University of Texas at Houston,Department of Diagnostic Radiology
[4] The University of Texas MD Anderson Cancer Center,Department of Imaging Physics
[5] The University of Texas MD Anderson Cancer Center,Department of Pathology
[6] The University of Texas MD Anderson Cancer Center,Department of Endocrinology Neoplasia and Hormonal Disorders
[7] The University of Texas MD Anderson Cancer Center,Department of Breast Medical Oncology
[8] Methodist Hospital Research Institute,Department of Emergency Medicine
[9] The University of Texas MD Anderson Cancer Center,undefined
[10] The University of Texas MD Anderson Cancer Center,undefined
[11] The University of Texas MD Anderson Cancer Center,undefined
[12] Present address: Department of Endocrine Neoplasia and Hormonal Disorders,undefined
[13] The University of Texas MD Anderson Cancer Center,undefined
[14] Houston,undefined
[15] Texas 77030,undefined
[16] USA.,undefined
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摘要
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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