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Molecular and Cellular Biology, September 2009, p. 4766-4777, Vol. 29, No. 17
0270-7306/09/$08.00+0 doi:10.1128/MCB.00087-09
Copyright © 2009, American Society for Microbiology. All Rights Reserved.
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Sylvester Comprehensive Cancer Center, Department of Medicine, and Department of Obstetrics and Gynecology, University of Miami School of Medicine, Miami, Florida 33136,1 Ovarian Cancer, Human Genetics, and Tumor Cell Biology Programs, Fox Chase Cancer Center, Philadelphia, Pennsylvania 191112
Received 19 January 2009/ Returned for modification 23 February 2009/ Accepted 25 June 2009
A prominent hallmark of most human cancer is aneuploidy, which is a result of the chromosomal instability of cancer cells and is thought to contribute to the initiation and progression of most carcinomas. The developmentally regulated GATA6 transcription factor is commonly lost in ovarian cancer, and the loss of its expression is closely associated with neoplastic transformation of the ovarian surface epithelium. In the present study, we found that reduction of GATA6 expression with small interfering RNA (siRNA) in human ovarian surface epithelial cells resulted in deformation of the nuclear envelope, failure of cytokinesis, and formation of polyploid and aneuploid cells. We further discovered that loss of the nuclear envelope protein emerin may mediate the consequences of GATA6 suppression. The nuclear phenotypes were reproduced by direct suppression of emerin with siRNA. Thus, we conclude that diminished expression of GATA6 leads to a compromised nuclear envelope that is causal for polyploidy and aneuploidy in ovarian tumorigenesis. The loss of emerin may be the basis of nuclear morphological deformation and subsequently the cause of aneuploidy in ovarian cancer cells.
Published ahead of print on 6 July 2009.
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