Cancer progression by reprogrammed BCAA metabolism in myeloid leukaemia
Ayuna Hattori,
Makoto Tsunoda,
Takaaki Konuma,
Masayuki Kobayashi,
Tamas Nagy,
John Glushka,
Fariba Tayyari,
Daniel McSkimming,
Natarajan Kannan,
Arinobu Tojo,
Arthur S. Edison and
Takahiro Ito ()
Additional contact information
Ayuna Hattori: Franklin College of Arts and Sciences, The University of Georgia
Makoto Tsunoda: Graduate School of Pharmaceutical Sciences, The University of Tokyo
Takaaki Konuma: The Institute of Medical Science, The University of Tokyo
Masayuki Kobayashi: The Institute of Medical Science, The University of Tokyo
Tamas Nagy: College of Veterinary Medicine, The University of Georgia
John Glushka: Complex Carbohydrate Research Center, The University of Georgia
Fariba Tayyari: Franklin College of Arts and Sciences, The University of Georgia
Daniel McSkimming: Franklin College of Arts and Sciences, The University of Georgia
Natarajan Kannan: Franklin College of Arts and Sciences, The University of Georgia
Arinobu Tojo: The Institute of Medical Science, The University of Tokyo
Arthur S. Edison: Franklin College of Arts and Sciences, The University of Georgia
Takahiro Ito: Franklin College of Arts and Sciences, The University of Georgia
Nature, 2017, vol. 545, issue 7655, 500-504
Abstract:
BCAT1, a cytosolic aminotransferase for branched-chain amino acids (BCAAs), is aberrantly activated and functionally required for disease progression in chronic myeloid leukaemia.
Date: 2017
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DOI: 10.1038/nature22314
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