STAT3 is constitutively activated and supports cell survival in association with survivin expression in gastric cancer cells

被引:0
|
作者
Naoki Kanda
Hiroshi Seno
Yoshitaka Konda
Hiroyuki Marusawa
Masashi Kanai
Toshio Nakajima
Tomoko Kawashima
Apichart Nanakin
Tateo Sawabu
Yoshito Uenoyama
Akira Sekikawa
Mayumi Kawada
Katsumasa Suzuki
Takahisa Kayahara
Hirokazu Fukui
Mitsutaka Sawada
Tsutomu Chiba
机构
[1] Kyoto University Graduate School of Medicine,Department of Gastroenterology and Hepatology
[2] Shogoin-Kawara-cho 54,undefined
[3] Sakyo-ku,undefined
来源
Oncogene | 2004年 / 23卷
关键词
STAT3; survivin; cancer; stomach;
D O I
暂无
中图分类号
学科分类号
摘要
Signal transduction and activator of transcription 3(STAT3) signaling is constitutively activated in various tumors, and is involved in cell survival and proliferation during oncogenesis. There are few reports, however, on the role of STAT3 signaling in gastric cancer. The aim of the present study was to clarify the role of STAT3 signaling in apoptosis and cellular proliferation in gastric cancer. Here we reported that STAT3 was constitutively activated in various human gastric cancer cells and its inhibition by ectopic dominant-negative STAT3 or Janus kinase inhibitor, tyrphostin AG490, induced apoptosis. Furthermore, STAT3 inhibition markedly decreased survivin expression, and forced expression of survivin rescued AGS cells from apoptosis induced by STAT3 inhibition. Although some reports demonstrated that the PI3K/Akt pathway regulates survivin expression, inhibition of the PI3K/Akt pathway did not affect survivin expression in AGS and MKN1 cells. Finally, activated form of STAT3, Tyr-705 phospho-stat3, was found in the nucleus of cancer cells in 11 of 40 (27.5%) human gastric cancer specimens. These findings suggest that constitutively activated STAT3 signaling supports gastric cancer cell survival in association with survivin expression.
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页码:4921 / 4929
页数:8
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