4.6 Article

MicroRNA-143 (miR-143) Regulates Cancer Glycolysis via Targeting Hexokinase 2 Gene

Journal

JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 287, Issue 27, Pages 23227-23235

Publisher

AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.M112.373084

Keywords

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Funding

  1. National Basic Research Program of China [2010CB912102, 2012CB910800]
  2. National Natural Science Foundation of China [30971461, 81101583]
  3. Science and Technology Commission of Shanghai Municipality [09JC1416300]
  4. Postdoctoral Research Program of Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences [2011KIP504]
  5. China Postdoctoral Science Foundation [20100480639]
  6. Sanofi-Aventis-Shanghai Institutes for Biological Sciences scholarship program

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High glycolysis, well known as Warburg effect, is frequently observed in a variety of cancers. Whether the deregulation of miRNAs contributes to the Warburg effect remains largely unknown. Because miRNA regulates gene expression at both mRNA and protein levels, we constructed a gene functional association network, which allows us to detect the gene activity instead of gene expression, to integratively analyze the microarray data for gene expression and miRNA expression profiling and identify glycolysis-related gene-miRNA pairs deregulated in cancer. Hexokinase 2 (HK2), coding for the first rate-limiting enzyme of glycolysis, is among the top list of genes predicted and potentially regulated by multiple miRNAs including miR-143. Interestingly, miR-143 expression was inversely associated with HK2 protein level but not mRNA level in human lung cancer samples. miR-143, down-regulated by mammalian target of rapamycin activation, reduces glucose metabolism and inhibits cancer cell proliferation and tumor formation through targeting HK2. Collectively, we have not only established a novel methodology for gene-miRNA pair prediction but also identified miR-143 as an essential regulator of cancer glycolysis via targeting HK2.

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