Elevated expression of eIT4E and FGF-2 isoforms during vascularization of breast carcinomas

被引:111
作者
Nathan, CA
Carter, P
Liu, L
Li, BD
Abreo, F
Tudor, A
Zimmer, SG
DeBenedetti, A
机构
[1] LOUISIANA STATE UNIV, MED CTR, DEPT BIOCHEM, SHREVEPORT, LA 71105 USA
[2] LOUISIANA STATE UNIV, MED CTR, DEPT OTOLARYNGOL, SHREVEPORT, LA USA
[3] LOUISIANA STATE UNIV, MED CTR, DEPT SURG, SHREVEPORT, LA 71130 USA
[4] LOUISIANA STATE UNIV, MED CTR, DEPT PATHOL, SHREVEPORT, LA 71130 USA
[5] UNIV KENTUCKY, MED CTR, LUCILLE P MARKEY CANC CTR, LEXINGTON, KY 40536 USA
关键词
eIF4E oncogene; FGF-2; isoforms; tumor vascularization; translation initiation; breast cancer progression; immunohistology;
D O I
10.1038/sj.onc.1201272
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
The translation initiation factor eIF4E is a novel protooncogene found over expressed in most breast carcinomas (Kerekatte et al., 1995), but the pathology where this elevation is initially manifested and its possible role in cancer progression are unknown, We report that eIF4E is markedly increased in vascularized malignant ductules of invasive carcinomas, whereas necrotic and avascular ductal carcinomas lit situ display significantly lower levels, eIF4E facilitates the synthesis of FGF-2, a powerful tumor angiogenic factor, Conversely, reducing eIF4E with antisense RNA in MDA-435 cells suppresses their tumorigenic and angiogenic properties, consistent with loss of FGF-2 synthesis, These findings suggest a causal role for eIF4E in tumor vascularization.
引用
收藏
页码:1087 / 1094
页数:8
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