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논문 기본 정보

자료유형
학술저널
저자정보
Song, Min-Ae (Functional Genomics Lab) Park, Jung-Hoon (Functional Genomics Lab) Ahn, Hee-Jeong (Department of Pathology, Bundang CHA Hospital, Pochon CHA University College of Medicine) Ko, Jung-Jae (CHA Research Institute, Bundang Campus, Pochon CHA University College of Medicine) Lee, Su-Man (Functional Genomics Lab)
저널정보
한국유전체학회 Genomics & informatics Genomics & informatics 제3권 제4호
발행연도
2005.1
수록면
154 - 158 (5page)

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Germ-line mutations of the BRCA1 gene confer an increased risk for breast and ovarian cancers. BRCA1 in female cells is directly related with the maintenance of the inactive X chromosome (Xi). The effect by the loss of the BRCA1 function on the X chromosome gene expression remains unclear in cancer cells. We attempted to investigate the expression pattern of the X-linked genes by performing BRCA1 knockdown via RNA interference in the MCF7 breast cancer cell line. The transcriptional and translational levels of BRCA1 were decreased over 95% in the MCF7 cells after BRCA1 knockdown. The expression patterns of one hundred ninety X-linked genes were profiled by the X chromosome-specific cDNA arrays. A total of seven percent of the X-linked genes (14/190) were aberrantly expressed by over 2-fold in the MCF7-BRCA1 knockdown cells, which contained two up-regulated genes (2/190, 1 %) and 12 down-regulated genes (12/190, 6.3%). It is interesting that 72% of the aberrantly expressed X-linked genes were located on the Xq (10/14,) region. Our data suggests that BRCA1 may not be important to maintain X chromosome inactivation in cancer because the BRCA1 knockdown did increase the expression of the only one percent of X-linked genes in the human breast cancer cells.

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