Ras-dependent induction of HIF-1a785 via the Raf/MEK/ERK pathway:: a novel mechanism of Ras-mediated tumor promotion

被引:83
作者
Lim, JH
Lee, ES
You, HJ
Lee, JW
Park, JW
Chun, YS
机构
[1] Seoul Natl Univ, Coll Med, Human Genome Res Inst, Seoul 110799, South Korea
[2] Seoul Natl Univ, Coll Med, Canc Res Inst, Seoul 110799, South Korea
[3] Chosun Univ, Coll Med, Dept Pharmacol, Kwangju 501759, South Korea
[4] Seoul Natl Univ, Coll Med, Dept Pharmacol, Seoul 110799, South Korea
关键词
HIF-1 alpha isoform; Ras signaling; phobol ester; EGF;
D O I
10.1038/sj.onc.1208003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hypoxia-inducible factor-1alpha (HIF-1alpha) plays crucial roles in tumor promotion by transactivating approximately 60 kinds of its target genes. Recently, we reported a novel splice variant HIF-1alpha(785), which is regulated primarily by phorbol ester. This variant can be stabilized under normoxic conditions because it loses an acetylation site Lys532. Its expression was found to promote xenografted tumor growth in nude mice. We here found that the Ras oncogene regulates HIF-1alpha(785) expression via the Raf/MEK/ERK pathway, and that both phorbol ester and epidermal growth factor also induced HIF-1alpha(785) via the same pathway. We also identified the nonhypoxic regulatory domain responsible for phorbol ester-induced HIF-1alpha(785) expression. These results imply that HIF-1alpha(785) may play an important role in tumor promotion mediated by the Ras oncogene, phorbol ester or tumor growth factors.
引用
收藏
页码:9427 / 9431
页数:5
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