BNIP3 expression is linked with hypoxia-regulated protein expression and with poor prognosis in non-small cell lung cancer\

被引:111
作者
Giatromanolaki, A
Koukourakis, MI
Sowter, HM
Sivridis, E
Gibson, S
Gatter, KC
Harris, AL
机构
[1] Democritus Univ Thrace, Dept Pathol, Alexandroupolis, Greece
[2] Democritus Univ Thrace, Dept Radiotherapy Oncol, Alexandroupolis, Greece
[3] John Radcliffe Hosp, Canc Res UK, Mol Oncol Labs, Inst Mol Med, Oxford OX3 9DU, England
[4] John Radcliffe Hosp, Dept Pathol, Nuffield Dept Clin Lab Sci, Oxford OX3 9DU, England
[5] Univ Manitoba, Manitoba Inst Cell Biol, Dept Biochem & Med Genet, Winnipeg, MB, Canada
关键词
D O I
10.1158/1078-0432.CCR-04-0076
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BNIP3 is a proapoptotic protein regulated by hypoxia-inducible factor 1. We analyzed BNIP3 expression in 105 tumor samples from early operable, non-small lung cancer and the relationship of expression to hypoxia-inducible factor 1(x, other hypoxia-regulated pathways, and prognosis. There was strong cytoplasmic expression in > 10 % of cells in 40 of 105 cases. BNIP3 expression was associated significantly with high hypoxia-inducible factor 1(x (P = 0.003), carbonic anhydrase 9 (P = 0.04), and was inversely associated with bcl-2 expression (P = 0.009). High BNIP3 expression was a major independent factor for overall survival. Thus, high expression of a hypoxia regulated proapoptotic pathway was associated with a selection of an aggressive phenotype in vivo.
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收藏
页码:5566 / 5571
页数:6
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