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Mechanisms of Cables 1 gene inactivation in human ovarian cancer development.

Authors :
Sakamoto H
Friel AM
Wood AW
Guo L
Ilic A
Seiden MV
Chung DC
Lynch MP
Serikawa T
Munro E
Oliva E
Orsulic S
Kirley SD
Foster R
Zukerberg LR
Rueda BR
Source :
Cancer biology & therapy [Cancer Biol Ther] 2008 Feb; Vol. 7 (2), pp. 180-88. Date of Electronic Publication: 2007 Nov 15.
Publication Year :
2008

Abstract

Cables 1, a cyclin-dependent kinase binding protein, is primarily involved in cell cycle regulation. Loss of nuclear Cables 1 expression is observed in human colon, lung and endometrial cancers. We previously reported that loss of nuclear Cables 1 expression was also observed with high frequency in a limited sample set of human ovarian carcinomas, although the mechanisms underlying loss of nuclear Cables 1 expression remained unknown. Our present objective was to examine Cables 1 expression in ovarian cancer in greater detail, and determine the predominant mechanisms of Cables 1 loss. We assessed potential genetic and epigenetic modifications of the Cables 1 locus through analyses of mutation, polymorphisms, loss of heterozygosity and DNA methylation. We observed a marked loss of nuclear Cables 1 expression in serous and endometrioid ovarian carcinomas that correlated with decreased Cables 1 mRNA levels. Although we detected no Cables 1 mutations, there was evidence of LOH at the Cables 1 locus and epigenetic modification of the Cables 1 promoter region in a subset of ovarian carcinomas and established cancer cell lines. From a functional perspective, over-expression of Cables 1 induced apoptosis, whereas, knockdown of Cables 1 negated this effect. Together these findings suggest that multiple mechanisms underlie the loss of Cables 1 expression in ovarian cancer cells, supporting the hypothesis that Cables 1 is a tumor suppressor in human ovarian cancer.

Details

Language :
English
ISSN :
1555-8576
Volume :
7
Issue :
2
Database :
MEDLINE
Journal :
Cancer biology & therapy
Publication Type :
Academic Journal
Accession number :
18059193
Full Text :
https://doi.org/10.4161/cbt.7.2.5253