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in Chemically Transformed Hamster Oral Keratinocytes1
Department of Oral Medicine and Oral Pathology, Harvard School of Dental Medicine, Boston, Massachusetts 02115
The cheek pouch of the Syrian hamster is an excellent tissue for the experimental induction of oral cancer by carcinogenic chemicals. Lysate prepared from a cell line (HCPC-1) derived from one of these hamster oral tumors greatly increased the growth of these oral tumor cells in vitro. We now show that the mitogenic substance, transforming growth factor
(TGF-
), is present in all of the chemically transformed hamster oral tumors examined (in vitro and in vivo). In no adult normal tissue of the Syrian hamster can we detect expression of TGF-
. TGF-
could be partly or wholly responsible for the mitogenic activity detected in the lysate of the chemically transformed hamster oral keratinocytes. Both normal and chemically transformed hamster oral keratinocytes express the receptor to epidermal growth factor. The consistent detection of TGF-
and epidermal growth factor receptor mRNAs in these hamster oral tumor cells suggests that an autocrine growth mechanism might be operative. This hamster cheek pouch oral cancer model can be used for the molecular analysis of how TGF-
and epidermal growth factor receptor might be involved in the malignant transformation of epithelial tissues.
1 Supported by Grant 0128 from the Smokeless Tobacco Research Council, Inc., and a Cancer Research Scholar Award from the American Cancer Society, Massachusetts Division.
2 To whom requests for reprints should be addressed.
Received 12/ 3/87. Revised 2/29/88. Accepted 3/ 7/88.
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