Literature DB >> 2230359

Two subclasses of EGF receptors in the human pancreatic cancer cell lines CAPAN-1 and MIA PaCa-2.

P Oustry1, A Estival, L Pradayrol, N Vaysse, F Clémente.   

Abstract

The existence of different classes of EGF receptors in human pancreatic cancer cells has yet not been determined. EGF binding to two cancer cell lines (CAPAN-1 and MIA PaCa-2) was studied. Two classes of EGF binding sites were characterized. The first class of EGF binding sites demonstrated a high affinity and low capacity for EGF, with a Kd of 0.25 +/- 0.11 nM, close to the concentration of EGF suggested to be present in human pancreatic juice. The second class of EGF binding sites had a lower affinity and a higher capacity for EGF, with Kd of 1.78 +/- 0.61 nM. The total number of EGF binding sites was about 40,000/cell. Treatment of the cells with a phorbol ester, TPA, caused a complete loss of the high affinity binding sites and also caused a decrease in the concentration of the lower affinity binding sites present on the cells. Interestingly, with the increasing age of the cells, the concentration of both the high and low affinity EGF binding sites was significantly decreased. In the presence or absence of fetal calf serum, EGF, at concentrations higher than 1.10(-10)M, exerted a dose-dependent mitogenic effect on the growth of the pancreatic cancer cells in culture. These data demonstrate the existence of two classes of binding sites for EGF on some human pancreatic cancer cells and a possible role of EGF in the growth of pancreatic tumors.

Entities:  

Mesh:

Substances:

Year:  1990        PMID: 2230359     DOI: 10.1007/bf02933046

Source DB:  PubMed          Journal:  Int J Pancreatol        ISSN: 0169-4197


  18 in total

1.  A study of the conditions and mechanism of the diphenylamine reaction for the colorimetric estimation of deoxyribonucleic acid.

Authors:  K BURTON
Journal:  Biochem J       Date:  1956-02       Impact factor: 3.857

2.  Different responses to EGF in two human carcinoma cell lines, A431 and UCVA-1, possessing high numbers of EGF receptors.

Authors:  S Gamou; Y S Kim; N Shimizu
Journal:  Mol Cell Endocrinol       Date:  1984-09       Impact factor: 4.102

3.  Further purification of epidermal growth factor by high-performance liquid chromatography.

Authors:  L M Matrisian; B R Larsen; J S Finch; B E Magun
Journal:  Anal Biochem       Date:  1982-09-15       Impact factor: 3.365

4.  Enhanced expression of epidermal growth factor receptor correlates with alterations of chromosome 7 in human pancreatic cancer.

Authors:  M Korc; P Meltzer; J Trent
Journal:  Proc Natl Acad Sci U S A       Date:  1986-07       Impact factor: 11.205

5.  Expression of epidermal growth factor receptor in human cultured cells and tissues: relationship to cell lineage and stage of differentiation.

Authors:  F X Real; W J Rettig; P G Chesa; M R Melamed; L J Old; J Mendelsohn
Journal:  Cancer Res       Date:  1986-09       Impact factor: 12.701

Review 6.  Epidermal growth factor and its receptor.

Authors:  G N Gill; P J Bertics; J B Santon
Journal:  Mol Cell Endocrinol       Date:  1987-06       Impact factor: 4.102

7.  Immunoreactive human epidermal growth factor in human pancreatic juice.

Authors:  Y Hirata; M Uchihashi; M Nakajima; T Fujita; S Matsukura
Journal:  J Clin Endocrinol Metab       Date:  1982-06       Impact factor: 5.958

8.  Epidermal growth factor binding and biologic effects on mouse pancreatic acini.

Authors:  C D Logsdon; J A Williams
Journal:  Gastroenterology       Date:  1983-08       Impact factor: 22.682

9.  Effects of epidermal growth factor, insulin and insulin-like growth factor I on rat pancreatic acinar cells cultured in serum-free medium.

Authors:  P M Brannon; K Hirschi; M Korc
Journal:  Pancreas       Date:  1988       Impact factor: 3.327

10.  Trophic action of epidermal growth factor on the pancreas and gastroduodenal mucosa in rats.

Authors:  A Dembiński; H Gregory; S J Konturek; M Polański
Journal:  J Physiol       Date:  1982-04       Impact factor: 5.182

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.