ENHANCED EXPRESSION OF AN INSULIN GROWTH FACTOR-LIKE BINDING-PROTEIN (MAC25) IN SENESCENT HUMAN MAMMARY EPITHELIAL-CELLS AND INDUCED EXPRESSION WITH RETINOIC ACID

被引:190
作者
SWISSHELM, K [1 ]
RYAN, K [1 ]
TSUCHIYA, K [1 ]
SAGER, R [1 ]
机构
[1] DANA FARBER CANC INST,DIV CANC GENET,BOSTON,MA 02115
关键词
BREAST CANCER; RETINOIDS; INSULIN GROWTH FACTOR-BINDING PROTEIN; SENESCENCE; DIFFERENTIAL DISPLAY;
D O I
10.1073/pnas.92.10.4472
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
mac25, the subject of this report, was selected by the differential display of mRNA method in a search for genes overexpressed in senescent human mammary epithelial cells. mac25 had previously been cloned as a discrete gene, preferentially expressed in normal, leptomeningial cells compared with meningioma tumors. mac25 is another member of the insulin growth factor-binding protein (IGFBP) family. Insulin-like growth factors are potent mitogens for mammary epithelial cells, and the IGFBPs have been shown to modulate this mitogenic activity. We report here that mac25, unlike most IGFBPs, is down-regulated at the transcription level in mammary carcinoma cell lines, suggesting a tumor-suppressor role. The gene was mapped to chromosome 4q12. We found that mac25 accumulates in senescent cells and is up-regulated in normal, growing mammary epithelial cells by all-trans-retinoic acid or the synthetic retinoid fenretinide. These findings suggest that mac25 may be a downstream effector of retinoid chemoprevention in breast epithelial cells and that its tumor-suppressive role may involve a senescence pathway.
引用
收藏
页码:4472 / 4476
页数:5
相关论文
共 41 条
[1]   INSULIN-LIKE GROWTH FACTOR-I (IGF-I) AND RETINOIC ACID MODULATION OF IGF-BINDING PROTEINS (IGFBPS) - IGFBP-2, IGFBP-3, AND IGFBP-4 GENE-EXPRESSION AND PROTEIN SECRETION IN A BREAST-CANCER CELL-LINE [J].
ADAMO, ML ;
SHAO, ZM ;
LANAU, F ;
CHEN, JC ;
CLEMMONS, DR ;
ROBERTS, CT ;
LEROITH, D ;
FONTANA, JA .
ENDOCRINOLOGY, 1992, 131 (04) :1858-1866
[2]   BASIC LOCAL ALIGNMENT SEARCH TOOL [J].
ALTSCHUL, SF ;
GISH, W ;
MILLER, W ;
MYERS, EW ;
LIPMAN, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410
[3]   INTERFERENCE OF THE IGF SYSTEM AS A STRATEGY TO INHIBIT BREAST-CANCER GROWTH [J].
ARTEAGA, CL .
BREAST CANCER RESEARCH AND TREATMENT, 1992, 22 (01) :101-106
[4]   DISTINCTIVE TRAITS OF NORMAL AND TUMOR-DERIVED HUMAN MAMMARY EPITHELIAL-CELLS EXPRESSED IN A MEDIUM THAT SUPPORTS LONG-TERM GROWTH OF BOTH CELL-TYPES [J].
BAND, V ;
SAGER, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (04) :1249-1253
[5]   LOSS OF P53 PROTEIN IN HUMAN PAPILLOMAVIRUS TYPE-16 E6-IMMORTALIZED HUMAN MAMMARY EPITHELIAL-CELLS [J].
BAND, V ;
DECAPRIO, JA ;
DELMOLINO, L ;
KULESA, V ;
SAGER, R .
JOURNAL OF VIROLOGY, 1991, 65 (12) :6671-6676
[6]   HUMAN RELAXINS - CHEMISTRY AND BIOLOGY [J].
BRYANTGREENWOOD, GD ;
SCHWABE, C .
ENDOCRINE REVIEWS, 1994, 15 (01) :5-26
[7]   INSULIN-LIKE GROWTH FACTOR-BINDING PROTEIN ENHANCEMENT OF INSULIN-LIKE GROWTH FACTOR-I (IGF-I)-MEDIATED DNA-SYNTHESIS AND IGF-I BINDING IN A HUMAN BREAST-CARCINOMA CELL-LINE [J].
CHEN, JC ;
SHAO, ZM ;
SHEIKH, MS ;
HUSSAIN, A ;
LEROITH, D ;
ROBERTS, CT ;
FONTANA, JA .
JOURNAL OF CELLULAR PHYSIOLOGY, 1994, 158 (01) :69-78
[8]  
CLEMMONS DR, 1993, ANN NY ACAD SCI, V692, P10
[9]  
DROP SLS, 1992, GROWTH REGULAT, V2, P69
[10]  
EDELHOFF S, 1994, ONCOGENE, V9, P665