Tyrosine Phosphorylation Inhibits PKM2 to Promote the Warburg Effect and Tumor Growth

Author:

Hitosugi Taro1,Kang Sumin1,Vander Heiden Matthew G.2,Chung Tae-Wook1,Elf Shannon1,Lythgoe Katherine1,Dong Shaozhong1,Lonial Sagar1,Wang Xu1,Chen Georgia Z.1,Xie Jianxin3,Gu Ting-Lei3,Polakiewicz Roberto D.3,Roesel Johannes L.4,Boggon Titus J.5,Khuri Fadlo R.1,Gilliland D. Gary6,Cantley Lewis C.2,Kaufman Jonathan1,Chen Jing1

Affiliation:

1. Winship Cancer Institute, Emory University School of Medicine, Atlanta, GA 30322, USA.

2. Dana-Farber Cancer Institute, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA 02115, USA.

3. Cell Signaling Technology, Inc. (CST), Danvers, MA 01923, USA.

4. Novartis Pharma AG, CH-4002 Basel, Switzerland.

5. Department of Pharmacology, Yale University School of Medicine, New Haven, CT 06520, USA.

6. Howard Hughes Medical Institute, Brigham and Women’s Hospital and Harvard Medical School, Boston, MA 02115, USA.

Abstract

Tyrosine phosphorylation of pyruvate kinase M2 gives tumor cells a metabolic advantage.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Cell Biology,Molecular Biology,Biochemistry

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