TY - JOUR
T1 - Pancreatic cancer cells require an EGF receptor-mediated autocrine pathway for proliferation in serum-free conditions
AU - Murphy, L. O.
AU - Cluck, M. W.
AU - Lovas, S.
AU - Ötvös, F.
AU - Murphy, R. F.
AU - Schally, A. V.
AU - Permert, J.
AU - Larsson, J.
AU - Knezetic, J. A.
AU - Adrian, T. E.
N1 - Funding Information:
The authors are grateful for the kind gifts of amphiregulin neutralizing monoclonal antibody 16.21.28 from Dr Bruce Cohen, Bristol Myers Squibb (Seattle, WA) and the IGF-I receptor monoclonal antibody a IR3 from Dr Steve Jacobs (Burroughs Wellcome Co., Research Triangle Park, NC). These studies were funded by grants from the Nebraska State Cancer and Smoking Related Disease Program (LB595), the Swedish Cancer Foundation (3450-B95-03xcc and 2870-B96-06xac) and the Carpenter Chair in Biochemistry, Creighton University.
PY - 2001/4/6
Y1 - 2001/4/6
N2 - In-vitro and in-vivo studies have shown that autocrine growth factors and receptors are frequently expressed in human malignancies, Few of these studies, however, provide evidence that the identified autocrine pathway is functional, In this study, a functional autocrine growth pathway in pancreatic cancer has been identified using an in-vitro cell culture System. When pancreatic cancer cells were grown without change of medium, proliferation was greater than when either medium was replaced frequently (HPAF, CAPAN-2, PANC-1 or SW1990) or cells were grown in the presence of the EGF receltor tyrosine kinase inhibitor AG1478 or the MEK inhibitor PD098059 (HPAF or CAPAN-2). Activity of extracellurar-regulated kinases (ERK) 1 and 2 and c-jun and c-fos mRNA levels were significantly elevated in CAPAN-2 cells cultured continuously in serum-free medium, Collectively, the observations indicate that the EGF receptor and the ERK MAP kinase pathway mediate autocrine signals. In contrast to previous reports, the GRP and IGF-I receltors were shown not to be required for autocrine effects on pancreatic cancer cell proliferation, Autocrine stimulation of the EGF receltor can contribute to sustained mitogenic activity and proliferation of pancreatic cancer cells.
AB - In-vitro and in-vivo studies have shown that autocrine growth factors and receptors are frequently expressed in human malignancies, Few of these studies, however, provide evidence that the identified autocrine pathway is functional, In this study, a functional autocrine growth pathway in pancreatic cancer has been identified using an in-vitro cell culture System. When pancreatic cancer cells were grown without change of medium, proliferation was greater than when either medium was replaced frequently (HPAF, CAPAN-2, PANC-1 or SW1990) or cells were grown in the presence of the EGF receltor tyrosine kinase inhibitor AG1478 or the MEK inhibitor PD098059 (HPAF or CAPAN-2). Activity of extracellurar-regulated kinases (ERK) 1 and 2 and c-jun and c-fos mRNA levels were significantly elevated in CAPAN-2 cells cultured continuously in serum-free medium, Collectively, the observations indicate that the EGF receptor and the ERK MAP kinase pathway mediate autocrine signals. In contrast to previous reports, the GRP and IGF-I receltors were shown not to be required for autocrine effects on pancreatic cancer cell proliferation, Autocrine stimulation of the EGF receltor can contribute to sustained mitogenic activity and proliferation of pancreatic cancer cells.
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U2 - 10.1054/bjoc.2001.1698
DO - 10.1054/bjoc.2001.1698
M3 - Article
C2 - 11286473
AN - SCOPUS:17744386907
VL - 84
SP - 926
EP - 935
JO - British Journal of Cancer
JF - British Journal of Cancer
SN - 0007-0920
IS - 7
ER -