| Abstract: |
Alteration in the expression of growth factors is widely accepted as being one of several critical defects in the generation of the malignant cell. In the present study, 19 human metastatic melanoma cell lines were compared to 14 normal human foreskin melanocyte cell lines for the production of RNA transcripts specific for 11 different growth factors. Using the extremely sensitive technique of polymerase chain reaction to amplify growth factor-specific complementary DNAs, we analyzed the following: transforming growth factor (TGF) types a, fi, tiâ¡a.nd /i.,acidic (a) fibroblast growth factor (FGF), basic (b) FGF, FGF-5, keratinocyte growth factor (KGF), HST, and platelet-derived growth factor (PDGF) types A and B. There were clear distinctions among the patterns of growth factor RNA expression by normal melanocytes and malignant melanoma cells. The prototypic melanocyte pattern of expression in cluded TGF0!, TGF/Sj, and KGF. A subset of melanocyte cell lines also expressed PDGFA transcripts. In contrast, melanoma cells characteris tically expressed RNA transcripts of TGF0, TGF&, TGF&, TGFa, bFGF, KGF, and PDGFA. Subsets of melanoma cell lines also expressed aFGF, FGF-5, and PDGFB. The results presented indicated that TGF/32, TGF«,and bFGF may be particularly important in melanomagenesis and that these, as well as FGF-5, aFGF, and PDGFB, can be used as markers of transformation in this tumor type. © 1991, American Association for Cancer Research. All rights reserved. |
| Keywords: |
genetics; molecular genetics; polymerase chain reaction; metabolism; melanoma; gene expression; melanocyte; melanocytes; tumor markers, biological; genetic transcription; transcription, genetic; pathology; tumor cells, cultured; tumor marker; physiology; cell transformation, neoplastic; rna; biosynthesis; molecular sequence data; cell culture; cell transformation; nucleotide sequence; fibroblast; fibroblasts; base sequence; growth substances; growth promotor; human; article; support, u.s. gov't, p.h.s.
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