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PMID: 3864531 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Characterization of autostimulatory and transforming growth factors from human melanoma cells.

Cancer research ·Vol. 45 ·No. 12 Pt 1 ·1985-12-00 ·Pages 6390-4

Richmond A, Lawson DH, Nixon DW, Chawla RK

Abstract

Serum-free growth of the human malignant melanoma cell line Hs0294 is associated with production of transforming growth factor-alpha and an autostimulatory melanoma mitogen (melanoma growth-stimulatory activity, MGSA). The transforming activity is characterized by stimulation of anchorage-independent growth of normal rat kidney fibroblasts and competition with 125I-epidermal growth factor for binding to normal rat kidney cells. The second activity, MGSA, stimulates the anchorage-dependent growth of human melanoma cells in serum-free culture medium. When acetic acid extracts of Hs0294 conditioned medium are subjected to Bio-Gel P-30 chromatography followed by reverse-phase high-pressure liquid chromatography, the majority of the transforming growth factor-alpha elutes at 30 +/- 4% acetonitrile, while the major peak of MGSA elutes at 35 +/- 3% acetonitrile. These data indicate that the anchorage-dependent serum-free growth of the Hs0294 human melanoma cell line is apparently dependent upon the autostimulatory melanoma mitogen, MGSA, which is separable from the 125I-epidermal growth factor competing activity produced by these cells.

MeSH Terms
Chromatography, Gel Chromatography, High Pressure Liquid Growth Substances/isolation & purification Humans Melanoma/analysis,pathology Peptides/isolation & purification Transforming Growth Factors
Chemicals
Growth Substances Peptides Transforming Growth Factors
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Richmond A
Lawson D H
Nixon D W
Chawla R K
Article Info
Journal
Cancer research
Abbr.
Cancer Res
ISSN
0008-5472
Published
1985-12-00
Pages
6390-4
Language
English
Region
United States
NLM ID
2984705R
Subset
IM
Grants
NCI NIH HHS · 1R23CA34590 · United States
NCRR NIH HHS · RR00039 · United States
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