ABERRANT SUBCELLULAR-LOCALIZATION OF BRCA1 IN BREAST-CANCER

被引:294
作者
CHEN, YM
CHEN, CF
RILEY, DJ
ALLRED, DC
CHEN, PL
VONHOFF, D
OSBORNE, CK
LEE, WH
机构
[1] UNIV TEXAS, HLTH SCI CTR, CTR MOLEC MED, INST BIOTECHNOL, SAN ANTONIO, TX 78245 USA
[2] UNIV TEXAS, HLTH SCI CTR, DEPT PATHOL, SAN ANTONIO, TX 78284 USA
[3] UNIV TEXAS, HLTH SCI CTR, DEPT MED, DIV MED ONCOL, SAN ANTONIO, TX 78284 USA
关键词
D O I
10.1126/science.270.5237.789
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The BRCA1 gene product was identified as a 220-kilodalton nuclear phosphoprotein in normal cells, including breast ductal epithelial cells, and in 18 of 20 tumor cell lines derived from tissues other than breast and ovary. In 16 of 17 breast and ovarian cancer lines and 17 of 17 samples of cells obtained from malignant effusions, however, BRCA1 localized mainly in cytoplasm. Absence of BRCA1 or aberrant subcellular location was also observed to a variable extent in histological sections of many breast cancer biopsies. These findings suggest that BRCA1 abnormalities may be involved in the pathogenesis of many breast cancers, sporadic as well as familial.
引用
收藏
页码:789 / 791
页数:3
相关论文
共 29 条
[1]   NUCLEAR LOCATION OF THE PUTATIVE TRANSFORMING PROTEIN OF AVIAN MYELOCYTOMATOSIS VIRUS [J].
ABRAMS, HD ;
ROHRSCHNEIDER, LR ;
EISENMAN, RN .
CELL, 1982, 29 (02) :427-439
[2]   CLONING OF HUMAN MINERALOCORTICOID RECEPTOR COMPLEMENTARY-DNA - STRUCTURAL AND FUNCTIONAL KINSHIP WITH THE GLUCOCORTICOID RECEPTOR [J].
ARRIZA, JL ;
WEINBERGER, C ;
CERELLI, G ;
GLASER, TM ;
HANDELIN, BL ;
HOUSMAN, DE ;
EVANS, RM .
SCIENCE, 1987, 237 (4812) :268-275
[3]   PUTATIVE NUCLEAR-LOCALIZATION SIGNALS (NLS) IN PROTEIN TRANSCRIPTION FACTORS [J].
BOULIKAS, T .
JOURNAL OF CELLULAR BIOCHEMISTRY, 1994, 55 (01) :32-58
[4]   BRCA1 - MORE THAN A HEREDITARY BREAST-CANCER GENE [J].
BOYD, J .
NATURE GENETICS, 1995, 9 (04) :335-336
[5]  
CAILLEAU R, 1978, IN VITRO CELL DEV B, V14, P911
[6]   MUTATIONS IN THE BRCA1 GENE IN FAMILIES WITH EARLY-ONSET BREAST AND OVARIAN-CANCER [J].
CASTILLA, LH ;
COUCH, FJ ;
ERDOS, MR ;
HOSKINS, KF ;
CALZONE, K ;
GARBER, JE ;
BOYD, J ;
LUBIN, MB ;
DESHANO, ML ;
BRODY, LC ;
COLLINS, FS ;
WEBER, BL .
NATURE GENETICS, 1994, 8 (04) :387-391
[7]   PHOSPHORYLATION OF THE RETINOBLASTOMA GENE-PRODUCT IS MODULATED DURING THE CELL-CYCLE AND CELLULAR-DIFFERENTIATION [J].
CHEN, PL ;
SCULLY, P ;
SHEW, JY ;
WANG, JYJ ;
LEE, WH .
CELL, 1989, 58 (06) :1193-1198
[8]  
Chen Y., UNPUB
[9]   HOT-SPOT P53 MUTANTS INTERACT SPECIFICALLY WITH 2 CELLULAR PROTEINS DURING PROGRESSION OF THE CELL-CYCLE [J].
CHEN, YM ;
CHEN, PL ;
LEE, WH .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (10) :6764-6772
[10]  
CLAUS EB, 1991, AM J HUM GENET, V48, P232