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BCKDK of BCAA Catabolism Cross-talking With the MAPK Pathway Promotes Tumorigenesis of Colorectal Cancer.
- Source :
-
EBioMedicine [EBioMedicine] 2017 Jun; Vol. 20, pp. 50-60. Date of Electronic Publication: 2017 May 04. - Publication Year :
- 2017
-
Abstract
- Branched-chain amino acids catabolism plays an important role in human cancers. Colorectal cancer is the third most commonly diagnosed cancer in males and the second in females, and the new global incidence is over 1.2 million cases. The branched-chain α-keto acid dehydrogenase kinase (BCKDK) is a rate-limiting enzyme in branched-chain amino acids catabolism, which plays an important role in many serious human diseases. Here we investigated that abnormal branched-chain amino acids catabolism in colorectal cancer is a result of the disease process, with no role in disease initiation; BCKDK is widely expressed in colorectal cancer patients, and those patients that express higher levels of BCKDK have shorter survival times than those with lower levels; BCKDK promotes cell transformation or colorectal cancer ex vivo or in vivo. Mechanistically, BCKDK promotes colorectal cancer by enhancing the MAPK signaling pathway through direct MEK phosphorylation, rather than by branched-chain amino acids catabolism. And the process above could be inhibited by a BCKDK inhibitor, phenyl butyrate.<br /> (Copyright © 2017 The Authors. Published by Elsevier B.V. All rights reserved.)
- Subjects :
- Animals
Cell Line, Tumor
Cell Transformation, Neoplastic genetics
Colorectal Neoplasms mortality
Colorectal Neoplasms pathology
Disease Models, Animal
Gene Expression
Humans
MAP Kinase Kinase 1 metabolism
Male
Mice
Phosphorylation
Prognosis
Protein Kinase Inhibitors pharmacology
Protein Kinases genetics
Amino Acids, Branched-Chain metabolism
Cell Transformation, Neoplastic metabolism
Colorectal Neoplasms etiology
Colorectal Neoplasms metabolism
MAP Kinase Signaling System
Protein Kinases metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 2352-3964
- Volume :
- 20
- Database :
- MEDLINE
- Journal :
- EBioMedicine
- Publication Type :
- Academic Journal
- Accession number :
- 28501528
- Full Text :
- https://doi.org/10.1016/j.ebiom.2017.05.001