4.6 Article

Metformin induces differentiation in acute promyelocytic leukemia by activating the MEK/ERK signaling pathway

Journal

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbrc.2012.05.001

Keywords

Metformin; Acute promyelocytic leukemia (APL); Apoptosis; Differentiation; Signaling pathway

Funding

  1. National Natural Science Foundation of China [81070427]
  2. National Science and Technology Major Project [2011ZX09302-007-04]
  3. Special Scientific Fund for Public Welfare Health Industry [201202017]
  4. Tianjin Applied Fundamental Research Planning Key Project [10JCZDJC 19600]

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Recent studies have shown that metformin, a widely used antidiabetic agent, may reduce the risk of cancer development. In this study, we investigated the antitumoral effect of metformin on both acute myeloid leukemia (AML) and acute promyelocytic leukemia (APL) cells. Metformin induced apoptosis with partial differentiation in an APL cell line, NB4, but only displayed a proapoptotic effect on several non-M3 AML cell lines. Further analysis revealed that a strong synergistic effect existed between metformin and all-trans retinoic acid (ATRA) during APL cell maturation and that metformin induced the hyper-phosphorylation of extracellular signal-regulated kinase (ERK) in APL cells. U0126, a specific MEK/ERK activation inhibitor, abrogated metformin-induced differentiation. Finally, we found that metformin induced the degradation of the oncoproteins PML-RAR alpha and c-Myc and activated caspase-3. In conclusion, these results suggest that metformin treatment may contribute to the enhancement of ATRA-induced differentiation in APL, which may deepen the understanding of APL maturation and thus provide insight for new therapy strategies. (c) 2012 Elsevier Inc. All rights reserved.

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