Two lines of normal human skin fibroblasts and five derivative lines transformed in culture to neoplastic cells by chemical carcinogens were compared with respect to chromatid breakage produced by exposure to low-intensi-
Light-induced chromatid damage in human skin fibroblasts in culture in relation to their neoplastic potential
✍ Scribed by Ram Parshad; Raymond Gantt; Katherine K. Sanford; Gary M. Jones; Richard F. Camalier
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- French
- Weight
- 597 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
✦ Synopsis
Skin fibroblasts from ataxia telangiectasia and xeroderma pigmentosum (XP) donors and from the XP sib (possible heterozygote), all genetically predisposed to a high risk of cancer, show an increased susceptibility to light-induced chromatid breaks after culture in vitro. Light-induced chromatid breaks were shown previously to result from generation of hydrogen peroxide (H20,) during light exposure. The level of susceptibility attained is significantly higher than that observed in 13 lines of fibroblasts from normal skin of donors ranging in age from 3 days t o 92 years or from fetal skin tested at various population doubling levels. Two lines of normal skin fibroblasts transformed by chemical carcinogens to neoplastic cells also show a significant increase in susceptibility as compared with their untransformed controls.
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## Abstract A metallothionein‐like protein (MTP) is synthesized in normal diploid human skin fibroblasts cultured in Zn‐ or Cu‐supplemented medium. Synthesis of MTP is not detected in cells cultured without metal supplementation of complete tissue‐culture medium. Cultured fibroblasts from patients