Effect of cyclin G2 on proliferative ability of SGC-7901 cell

World J Gastroenterol. 2004 May 1;10(9):1357-60. doi: 10.3748/wjg.v10.i9.1357.

Abstract

Aim: To study the effect of cyclin G2 on proliferation of gastric adenocarcinoma cell line-SGC-7901 cell in vitro.

Methods: By use of cation lipofectamine transfection reagent, the pIRES-G2 and pIRESneo plasmids were transferred into SGC-7901cell line. Anticlones were selected by G418. Positive clones were observed and counted using Giemsa staining. Cell proliferative ability was assayed by MTT.

Results: (1) The clone number of pIRES-G2 group decreased, clone volume reduced. The number of cell clones in pIRESneo group was 87+/-3, that of pIRES-G2 group was 53+/-4, occupying 60.1% of pIRESneo group, there was significant difference obviously (P<0.01, t=15.45). (2) The average absorbance of clone cell obtained by stable transfection of pIRES-G2 at 570 nm was 1.6966+/-0.2125, the average absorbance of clone cell obtained by stable transfection of pIRESneo at 570 nm was 2.1182+/-0.3675, there was significant difference between them (P<0.01, t=3.412).

Conclusion: Cyclin G2 can inhibit SGC-7901cell proliferative ability obviously, it may be a negative regulator in cell cycle regulation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / metabolism
  • Cell Cycle / physiology
  • Cell Division / physiology*
  • Cell Line, Tumor
  • Cyclin G2
  • Cyclins / genetics
  • Cyclins / metabolism*
  • Humans
  • Stomach Neoplasms / metabolism
  • Transfection

Substances

  • CCNG2 protein, human
  • Cyclin G2
  • Cyclins