Cloning and characterization of a novel gene that is regulated by estrogen and is associated with mammary gland carcinogenesis

被引:10
作者
Marcantonio, D
Chalifour, LE
Alaoui-Jamali, MA
Alpert, L
Huynh, HT
机构
[1] McGill Univ, Lady Davis Inst Med Res, Sir Mortimer B Davis Jewish Gen Hosp, Dept Med, Montreal, PQ H3T 1E2, Canada
[2] McGill Univ, Dept Pharmacol & Therapeut, Montreal, PQ H3T 1E2, Canada
[3] McGill Univ, Dept Pathol & Oncol, Montreal, PQ H3T 1E2, Canada
关键词
D O I
10.1210/en.142.6.2409
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Estrogens play a role in mammary gland function and are implicated in mammary carcinogenesis. We report the cloning of a novel gene [steroid-sensitive gene 1 (SSG1)] that is regulated by E, in the rat uterus and mammary gland. The full-length SSG1 complementary DNA has an open reading frame of 1158 nucleotides encoding a putative protein of 385 amino acids. A SSG1-specific antibody recognizes a 40-kDa protein localized to myoepithelial cells of normal mammary tissue and to endothelial cells of 7,12-dimethylbenz(a)antracene-induced mammary tumors. Treatment of rats with E-2 at 1.2 or 2.4 mug/kg.day for 21 days increases SSG1 protein levels in mammary tissue by 16-fold compared with controls. Removal of E-2 after a 14-day treatment decreases SSG1 protein levels 6-fold and 3-fold at 120 and 144 h, respectively. Treatment of rats with the estrogen antagonists tamoxifen or ICI 182,780 did not affect SSG1 protein levels compared with controls. SSG1 protein levels in 7,12-dimethylbenz(a)antracene-induced rat mammary tumors were 23-fold greater than SSG1 levels in resting mammary tissue, and 8-fold higher than protein levels expressed in lactating mammary glands. We propose that SSG1 plays a role in estrogen functions, and its overexpression is correlated with mammary carcinogenesis.
引用
收藏
页码:2409 / 2418
页数:10
相关论文
共 41 条
[1]
CHARACTERIZATION OF THE PROXIMAL ESTROGEN-RESPONSIVE ELEMENT OF HUMAN CATHEPSIN-D GENE [J].
AUGEREAU, P ;
MIRALLES, F ;
CAVAILLES, V ;
GAUDELET, C ;
PARKER, M ;
ROCHEFORT, H .
MOLECULAR ENDOCRINOLOGY, 1994, 8 (06) :693-703
[2]
Over expression of vascular endothelial growth factor and its receptor during the development of estrogen-induced rat pituitary tumors may mediate estrogen-initiated tumor angiogenesis [J].
Banerjee, SK ;
Sarkar, DK ;
Weston, AP ;
De, A ;
Campbell, DR .
CARCINOGENESIS, 1997, 18 (06) :1155-1161
[3]
EXPRESSION OF TRANSFORMING GROWTH FACTOR-ALPHA AND ITS MESSENGER RIBONUCLEIC-ACID IN HUMAN-BREAST CANCER - ITS REGULATION BY ESTROGEN AND ITS POSSIBLE FUNCTIONAL-SIGNIFICANCE [J].
BATES, SE ;
DAVIDSON, NE ;
VALVERIUS, EM ;
FRETER, CE ;
DICKSON, RB ;
TAM, JP ;
KUDLOW, JE ;
LIPPMAN, ME ;
SALOMON, DS .
MOLECULAR ENDOCRINOLOGY, 1988, 2 (06) :543-555
[4]
DAUVOIS S, 1993, J CELL SCI, V106, P1377
[5]
FAUCHER C, 1993, J BIOL CHEM, V268, P15168
[6]
Folkman J, 1976, Int Rev Exp Pathol, V16, P207
[7]
FUKUSHO K, 1985, B NATL RES I AQUACUL, V7, P29
[8]
Gazzaley AH, 1996, J NEUROSCI, V16, P6830
[9]
Estrogen receptor β:: Re-evaluation of estrogen and antiestrogen signaling [J].
Giguère, V ;
Tremblay, A ;
Tremblay, GB .
STEROIDS, 1998, 63 (5-6) :335-339
[10]
TUMOR-GROWTH AND NEOVASCULARIZATION - EXPERIMENTAL MODEL USING RABBIT CORNEA [J].
GIMBRONE, MA ;
COTRAN, RS ;
LEAPMAN, SB ;
FOLKMAN, J .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1974, 52 (02) :413-427