Cripto: roles in mammary cell growth, survival, differentiation and transformation

被引:42
作者
Niemeyer, CC
Persico, MG
Adamson, ED
机构
[1] Burnham Inst, La Jolla Canc Res Ctr, La Jolla, CA 92037 USA
[2] Int Inst Genet & Biophys, I-80125 Naples, Italy
关键词
retroviruses; overexpression; antisense; milk proteins; apoptosis; anchorage independent growth; tumorigenicity;
D O I
10.1038/sj.cdd.4400368
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cripto-1 (Cr-1) protein, encoded by the teratocarcinoma-derived growth factor gene (TDGF-1), is highly correlated with transformation in breast cancer. Eighty-two percent of breast carcinomas express Cr-1 whereas it is undetected in normal human breast tissue. We confirmed and extended findings that Cr-1 protein is expressed during the pregnancy and lactating stages of normal murine mammary glands but is barely detectable in glands from virgin animals and is undetectable in involuted glands. Cr-1 was found to be expressed in CID 9 cells, a line of mammary epithelial cells derived from 14.5 day pregnant mice and we have used these cells to investigate the roles of this gene. Exogenous mouse Cr-1 expression from a retroviral vector caused CID 9 cells to grow at an increased rate and to increased cell densities compared to parental and control cells. CID 9 cells overexpressing Cr-1 did not differentiate efficiently. Infection of CID 9 cells with a Cr-1 antisense vector caused these cells to change in morphology, to grow slowly, to undergo apoptosis at a higher rate and to achieve lower saturation densities but the cells were still capable of differentiating. We concluded that Cr-1 is an autocrine growth factor for normal breast cells, that when over expressed stimulates excessive cell proliferation at the expense of differentiation. In transplantation studies, Cr-1 over-expression stimulated the growth and survival of mammary cells, but did not stimulate tumorigenesis in vivo.
引用
收藏
页码:440 / 449
页数:10
相关论文
共 37 条
[1]  
AGUILARCORDOVA E, 1991, ONCOGENE, V6, P1601
[2]   Expression of teratocarcinoma-derived growth factor-1 (TDGF-1) in testis germ cell tumors and its effects on growth and differentiation of embryonal carcinoma cell line NTERA2/D1 [J].
Baldassarre, G ;
Romano, A ;
Armenante, F ;
Rambaldi, M ;
Paoletti, I ;
Sandomenico, C ;
Pepe, S ;
Staibano, S ;
Salvatore, G ;
DeRosa, G ;
Persico, MG ;
Viglietto, G .
ONCOGENE, 1997, 15 (08) :927-936
[3]   RECENT ADVANCES IN RETROVIRUS VECTOR TECHNOLOGY [J].
BORISLAWRIE, KA ;
TEMIN, HM .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1993, 3 (01) :102-109
[4]   INDUCTION OF MOUSE MAMMARY-TUMORS IN A TRANSPLANTATION SYSTEM BY THE SEQUENTIAL INTRODUCTION OF THE MYC AND RAS ONCOGENES [J].
BRADBURY, JM ;
SYKES, H ;
EDWARDS, PAW .
INTERNATIONAL JOURNAL OF CANCER, 1991, 48 (06) :908-915
[5]  
BRANDT R, 1994, J BIOL CHEM, V269, P17320
[6]  
CIARDIELLO F, 1991, CANCER RES, V51, P1051
[7]   MOLECULAR CHARACTERIZATION OF A GENE OF THE EGF FAMILY EXPRESSED IN UNDIFFERENTIATED HUMAN NTERA2 TERATOCARCINOMA CELLS [J].
CICCODICOLA, A ;
DONO, R ;
OBICI, S ;
SIMEONE, A ;
ZOLLO, M ;
PERSICO, MG .
EMBO JOURNAL, 1989, 8 (07) :1987-1991
[8]   INHIBITION OF MOUSE MAMMARY DUCTAL MORPHOGENESIS AND DOWN-REGULATION OF THE EGF RECEPTOR BY EPIDERMAL GROWTH-FACTOR [J].
COLEMAN, S ;
DANIEL, CW .
DEVELOPMENTAL BIOLOGY, 1990, 137 (02) :425-433
[9]   EPITHELIAL MOUSE MAMMARY CELL-LINE EXHIBITING NORMAL MORPHOGENESIS INVIVO AND FUNCTIONAL-DIFFERENTIATION INVITRO [J].
DANIELSON, KG ;
OBORN, CJ ;
DURBAN, EM ;
BUTEL, JS ;
MEDINA, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (12) :3756-3760
[10]  
Desprez Pierre-Yves, 1993, Molecular and Cellular Differentiation, V1, P99