[Effect of down-regulation of histone deacetylase 2 protein expression on cell proliferation and cell cycle in cervical carcinoma]

Zhonghua Bing Li Xue Za Zhi. 2012 Jul;41(7):466-9. doi: 10.3760/cma.j.issn.0529-5807.2012.07.008.
[Article in Chinese]

Abstract

Objective: To study the effect of down-regulation of histone deacetylase 2 (HDAC2) expression on cell proliferation and cell cycle in cervical carcinoma cell lines HeLa.

Methods: HDAC2 siRNA and control siRNA were transfected to HeLa cells. CCK-8 and flow cytometry were used to analyze the changes of cell proliferation and cell cycle, respectively. Western blot was employed to detect the changes of cell proliferation and cell cycle-related proteins.

Results: HDAC2 siRNA significantly down-regulated the expression of HDAC2 protein in HeLa cells, resulting in marked inhibition of cell proliferation. In addition, the percentage of cells in G(0)/G(1) phase in HDAC2 siRNA group (63.3% ± 2.0%) was significantly higher than that in untreated group (29.3% ± 1.7%) or control siRNA group (29.4% ± 1.7%), F = 354.181, P = 0.000. Furthermore, Western blot demonstrated that down-regulation of HDAC2 expression decreased the expression of cyclin D1, cyclin E and CDK2 proteins but increased the expression of p21 protein.

Conclusions: Down-regulation of HDAC2 expression mediates proliferation inhibition and cell cycle arrest. It is associated with decrease in cyclin D1, cyclin E and CDK2 protein expression and increase in p21 protein expression.

Publication types

  • English Abstract
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Cycle*
  • Cell Proliferation*
  • Cyclin D1 / metabolism
  • Cyclin E / metabolism
  • Cyclin-Dependent Kinase 2 / metabolism
  • Down-Regulation
  • HeLa Cells
  • Histone Deacetylase 2 / genetics
  • Histone Deacetylase 2 / metabolism*
  • Humans
  • Oncogene Proteins / metabolism
  • Proto-Oncogene Proteins p21(ras) / metabolism
  • RNA, Small Interfering / genetics
  • Transfection

Substances

  • CCND1 protein, human
  • CCNE1 protein, human
  • Cyclin E
  • Oncogene Proteins
  • RNA, Small Interfering
  • Cyclin D1
  • CDK2 protein, human
  • Cyclin-Dependent Kinase 2
  • HDAC2 protein, human
  • Histone Deacetylase 2
  • Proto-Oncogene Proteins p21(ras)