期刊
JOURNAL OF BIOCHEMISTRY
卷 152, 期 5, 页码 383-385出版社
OXFORD UNIV PRESS
DOI: 10.1093/jb/mvs106
关键词
Akt; cancer stem cell; CML; MMP-9; TGF-beta
Recent data have shown that transforming growth factor-beta (TGF-beta) plays bi-directional roles in the maintenance of cancer stem cells in a cell-type and context-dependent manner. Zhu et al. (TGF-beta 1-induced PI3K/Akt/NF-kappa B/MMP9 signalling pathway is activated in Philadelphia chromosome-positive chronic myeloid leukaemia hemangioblasts. J. Biochem. 2011;149:405-414) studied the functions of TGF-beta in hemangioblasts from patients with chronic myeloid leukemia (CML), which displayed properties of leukemia-initiating cells. They have shown that the BCR/ABL oncoprotein induced the production of TGF-beta in the CML hemangioblasts, and that TGF-beta activated the phosphoinositide 3-kinase-Akt-NF-kappa B pathway in these cells. Activation of this pathway enhanced the production of matrix metalloproteinase-9 leading to increased synthesis of soluble Kit ligand and intercellular adhesion molecule-1. TGF-beta is known to maintain the CML-initiating cells through the Akt-FoxO pathway. Together, these findings suggest that TGF-beta may exhibit multiple functions in progression of CML through acting on leukemia-initiating cells.
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