## Abstract Insulin‐like growth factor binding protein‐3 (IGFBP‐3) has been proposed to mediate the growth inhibitory effects of transforming growth factor (TGF)‐β in breast and prostate cancer cells. Both TGF‐β and exogenous IGFBP‐3 inhibit DNA synthesis in Mv1 mink lung epithelial cells (CCL64).
Isolation and characterization of mink lung epithelial cell mutants resistant to transforming growth factor β
✍ Scribed by Michael Chinkers
- Publisher
- John Wiley and Sons
- Year
- 1987
- Tongue
- English
- Weight
- 604 KB
- Volume
- 130
- Category
- Article
- ISSN
- 0021-9541
No coin nor oath required. For personal study only.
✦ Synopsis
Mink lung epithelial cells resistant to growth inhibition by transforming growth factor P (TGF-P) have been isolated by chemical mutagenesis and growth in the presence of platelet extracts enriched in TGF-P. Several resistant clones were isolated, at least one of which stably retained its resistance to TGF-P when grown in the absence of the factor. The cells of this clone were similar to the parent cells in morphology and growth properties. However, unlike the parent cells, the resistant cells did not show any of the following responses to TGF-P: (1) inhibition of DNA synthesis and proliferation; (2) morphological changes involving increased cell spreading; or (3) stimulation of synthesis of a 48-kilodalton secreted protein. The resistant cells do, however, retain a functional TGF-P receptor. The TGF-P resistant cell lines may be useful in genetic studies designed to identify the biochemical events required for inhibition of epithelial cell growth by this factor.
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