Multinuclear giant cell formation is enhanced by down-regulation of Wnt signaling in gastric cancer cell line, AGS

  • Kim, SM; 
  • Kim, R; 
  • Ryu, JH; 
  • Jho, EH; 
  • Song, KJ; 
  • ... Kee, SH; 
  • 외 1명
Citations

WEB OF SCIENCE

15
Citations

SCOPUS

16

초록

AGS cells, which were derived from malignant gastric adenocarcinoma tissue, lack E-cadherin-mediated cell adhesion but have a high level of nuclear beta-catenin, which suggests altered Wnt signal. In addition, approximately 5% of AGS cells form multinuclear giant cells in the routine culture conditions, while taxol treatment causes most AGS cells to become giant cells. The observation of reduced nuclear beta-catenin levels in giant cells induced by taxol treatment prompted us to investigate the relationship between Wnt signaling and giant cell formation. After overnight serum starvation, the shape of AGS cells became flattened, and this morphological change was accompanied by decrease in Myc expression and an increase in the giant cell population. Lithium chloride treatment, which inhibits GSK3 beta activity, reversed these serum starvation effects, which suggests an inverse relationship between Wnt signaling and giant cell formation. Furthermore, the down-regulation of Wnt signaling caused by the over-expression of ICAT, E-cadherin, and Axin enhanced giant cell fort-nation. Therefore, down-regulation of Wnt signaling may be related to giant cell formation, which is considered to be a survival mechanism against induced cell death. (c) 2005 Elsevier Inc. All rights reserved.

키워드

AGS cells; Wnt signaling; giant cell formation; beta-catenin; E-cadherin; ICAT; ADENOMATOUS-POLYPOSIS-COLI; MITOTIC CHECKPOINT GENES; BETA-CATENIN; SUPPRESSOR GENE; EXPRESSION; MUTATIONS; ADHESION; P53; PROGRESSION; PROTEIN
제목
Multinuclear giant cell formation is enhanced by down-regulation of Wnt signaling in gastric cancer cell line, AGS
저자
Kim, SM; Kim, R; Ryu, JH; Jho, EH; Song, KJ; Jang, SI; Kee, SH
DOI
10.1016/j.yexcr.2005.04.002
발행일
2005-08-01
유형
Article
저널명
Experimental Cell Research
권
308
호
1
페이지
18 ~ 28