The epidermal growth factor receptor couples transforming growth factor-alpha, heparin-binding epidermal growth factor-like factor, and amphiregulin to Neu, ErbB-3, and ErbB-4

被引:152
作者
Riese, DJ
Kim, ED
Elenius, K
Buckley, S
Klagsbrun, M
Plowman, GD
Stern, DF
机构
[1] YALE UNIV,SCH MED,DEPT PATHOL,NEW HAVEN,CT 06520
[2] CHILDRENS HOSP,DEPT SURG RES,BOSTON,MA 02115
[3] HARVARD UNIV,SCH MED,BOSTON,MA 02115
[4] BRISTOL MYERS SQUIBB PHARMACEUT RES INST,SEATTLE,WA 98121
[5] SUGEN INC,REDWOOD CITY,CA 94063
关键词
D O I
10.1074/jbc.271.33.20047
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
The epidermal growth factor (EGF) family hormones amphiregulin (AR), transforming growth factor-alpha (TGF-alpha), and heparin-binding EGF-like growth factor (HB-EGF) are thought to play significant roles in the genesis or progression of a number of human malignancies. However, the ability of these ligands to activate all four erbB family receptors has not been evaluated. Therefore, we have assessed the stimulation of erbB family receptor tyrosine phosphorylation by these hormones in a panel of mouse Ba/F3 cell lines expressing the four erbB family receptors, singly and in pairwise combinations. We also measured the stimulation of interleukin-3-independent survival or proliferation in this panel of Ba/F3 cell lines to compare the patterns of erbB family receptor coupling to physiologic responses induced by these peptides. EGF, TGF-alpha, AR, and HB-EGF all stimulated qualitatively similar patterns of erbB family receptor tyrosine phosphorylation and coupling to physiologic responses. Therefore, EGF, TGF-alpha, AR, and HB-EGF are functionally identical in this model system and behave differently from the EGF family hormones beta-cellulin and neuregulins.
引用
收藏
页码:20047 / 20052
页数:6
相关论文
共 46 条
[1]   TUMOR PROMOTER AND EPIDERMAL GROWTH-FACTOR STIMULATE PHOSPHORYLATION OF THE C-ERBB-2-GENE PRODUCT IN MKN-7 HUMAN ADENOCARCINOMA CELLS [J].
AKIYAMA, T ;
SAITO, T ;
OGAWARA, H ;
TOYOSHIMA, K ;
YAMAMOTO, T .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (03) :1019-1026
[2]  
ALIMANDI M, 1995, ONCOGENE, V10, P1813
[3]   THE STRUCTURAL BASIS FOR THE SPECIFICITY OF EPIDERMAL GROWTH-FACTOR AND HEREGULIN BINDING [J].
BARBACCI, EG ;
GUARINO, BC ;
STROH, JG ;
SINGLETON, DH ;
ROSNACK, KJ ;
MOYER, JD ;
ANDREWS, GC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (16) :9585-9589
[4]  
BEERLI RR, 1995, MOL CELL BIOL, V15, P6496
[5]   HEREGULIN STIMULATES MITOGENESIS AND PHOSPHATIDYLINOSITOL 3-KINASE IN MOUSE FIBROBLASTS TRANSFECTED WITH ERBB2/NEU AND ERBB3 [J].
CARRAWAY, KL ;
SOLTOFF, SP ;
DIAMONTI, AJ ;
CANTLEY, LC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (13) :7111-7116
[6]  
CARRAWAY KL, 1994, J BIOL CHEM, V269, P14303
[7]   THE EPIDERMAL GROWTH-FACTOR RECEPTOR AND THE PRODUCT OF THE NEU PROTOONCOGENE ARE MEMBERS OF A RECEPTOR TYROSINE PHOSPHORYLATION CASCADE [J].
CONNELLY, PA ;
STERN, DF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (16) :6054-6057
[8]   THE CARBOXY-TERMINAL DOMAINS OF ERBB-2 AND EPIDERMAL GROWTH-FACTOR RECEPTOR EXERT DIFFERENT REGULATORY EFFECTS ON INTRINSIC RECEPTOR TYROSINE KINASE FUNCTION AND TRANSFORMING ACTIVITY [J].
DIFIORE, PP ;
SEGATTO, O ;
LONARDO, F ;
FAZIOLI, F ;
PIERCE, JH ;
AARONSON, SA .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (06) :2749-2756
[9]   EGF RECEPTOR AND ERBB-2 TYROSINE KINASE DOMAINS CONFER CELL SPECIFICITY FOR MITOGENIC SIGNALING [J].
DIFIORE, PP ;
SEGATTO, O ;
TAYLOR, WG ;
AARONSON, SA ;
PIERCE, JH .
SCIENCE, 1990, 248 (4951) :79-83
[10]   HETERODIMERIZATION AND FUNCTIONAL INTERACTION BETWEEN EGF RECEPTOR FAMILY MEMBERS - A NEW SIGNALING PARADIGM WITH IMPLICATIONS FOR BREAST-CANCER RESEARCH [J].
EARP, HS ;
DAWSON, TL ;
LI, X ;
YU, H .
BREAST CANCER RESEARCH AND TREATMENT, 1995, 35 (01) :115-132