EPIDERMAL GROWTH-FACTOR AND TRANSFORMING GROWTH-FACTOR-ALPHA CHARACTERISTICS OF HUMAN ORAL-CARCINOMA CELL-LINES


Autoria(s): Prime, S. S.; Game, S. M.; Matthews, J. B.; Stone, A.; Donnelly, M. J.; Yeudall, W. A.; PATEL, V; Sposto, R.; Silverthorne, A.; Scully, C.
Contribuinte(s)

Universidade Estadual Paulista (UNESP)

Data(s)

20/05/2014

20/05/2014

01/01/1994

Resumo

This study examined the expression of epidermal growth factor (EGF) cell-surface receptors, the response to exogenous ligand and the autocrine production of transforming growth factor a (TGF-a) in normal and carcinoma-derived human oral keratinocytes. One of eight malignant cell lines overexpressed EGF receptors, while the remainder expressed receptor numbers similar to normal cells. Exogenous EGF stimulated incorporation of tritiated thymidine in a dose-dependent manner. In keratinocytes expressing normal numbers of EGF receptors, the cellular response to exogenous EGF correlated positively with total EGF receptor number. SCC-derived keratinocytes produced more TGF-a than normal cells. There was no statistical correlation between the autocrine production of TGF-a, EGF cell-surface receptor expression and cellular response to exogenous EGF. While the growth-stimulatory effects of exogenous TGF-cl were inhibited by the addition of a neutralising antibody, the presence of this antibody in conditioned medium failed to produce a similar decrease in growth. The results indicate that overexpression of EGF receptors is not an invariable characteristic of human oral squamous carcinoma-derived cell lines. Further, the contribution of TGF-a to the growth of normal and carcinoma-derived human oral keratinocytes in vitro may be less significant than previously documented.

Formato

8-15

Identificador

http://dx.doi.org/10.1038/bjc.1994.2

British Journal of Cancer. Basingstoke: Stockton Press, v. 69, n. 1, p. 8-15, 1994.

0007-0920

http://hdl.handle.net/11449/34469

10.1038/bjc.1994.2

WOS:A1994MQ28700002

Idioma(s)

eng

Publicador

Stockton Press

Relação

British Journal of Cancer

Direitos

closedAccess

Tipo

info:eu-repo/semantics/article