[Effect of microRNA-17-92 cluster on the biological characteristics of K562 cells and its mechanisms]

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2014 Feb;22(1):20-4. doi: 10.7534/j.issn.1009-2137.2014.01.005.
[Article in Chinese]

Abstract

The objective of this study was to explore the effects of microRNA-17-92 on the biological characteristics of K562 cells. The expression of miR-17-92 in K562 cells transfected with miRNA-17-92 mimic was detected by real time PCR. The effect of microRNA-17-92 on K562 cell proliferation was detected by CCK-8 method. Apoptosis of K562 cells was detected by Annexin V-PI labeling. Cell cycle distribution was determined by using flow cytometry. Western blot was performed to determine the protein levels of Crk. The results indicated that the transfection with miR-17-92 mimic increased expression of mature miR-17-92 in K562 cells. Compared with control group, cell proliferation and cell amount in S-phase of miR-17-92 mimic transfected group significantly increased, cell apoptosis decreased. The expression of signal connector protein Crk was greatly up-regulated in miR-17-92-mimic-transfected K562 cells. It is concluded that miR-17-92 can promote proliferation, inhibit apoptosis and regulate the cell cycle of K562 cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis
  • Cell Cycle
  • Cell Proliferation
  • Gene Expression Regulation, Leukemic
  • HL-60 Cells
  • Humans
  • K562 Cells
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / genetics*
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / metabolism
  • MicroRNAs / genetics*
  • RNA, Long Noncoding
  • Transfection

Substances

  • MIR17HG, human
  • MicroRNAs
  • RNA, Long Noncoding