## Abstract Rodent cell lines can develop resistance to doxorubicin and methotrexate during hypoxic stress. This has so far not been observed in human tumor cell lines. The purpose of our communication is to show that doxorubicin and methotrexate resistance can also develop in human melanoma cells
Melphalan-induced chromosome damage in sensitive and resistant human melanoma cell lines
β Scribed by P. G. Parsons; Leanne Morrison
- Publisher
- John Wiley and Sons
- Year
- 1978
- Tongue
- French
- Weight
- 492 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Twelve consecutive treatments of a human melanoma cell line (MM253) with melphalan gave a subline (MM253β12M) which was five times more resistant to melphalan with respect to survival. In contrast to mustardβresistant rodent cells, the MM253β12M line had a higher stemline number than the parent line while growth rate and cell and colony morphology were unchanged. A further melphalan treatment following attempted mutagenesis with UV did not increase resistance. In a comparison of these two lines with two melanoma lines derived from other patients and the rat XC line, resistance was correlated with lower frequency of melphalanβinduced chromosome aberrations, determined 48 h after a 4βh exposure to melphalan(3 ΞΌg/ml). In the two cell lines studied, aberrationβfree metaphase cells from treated culture had fewer chromosomes than untreated cells. DNA synthesis studied in the 4β to 72βh period after treatment was inhibited to the same extent in MM253 and MM253β12M cells at 4 ΞΌg/ml but to a greater extent in the sensitive line at 0.1β1.5 ΞΌg/ml. During the first hour of treatment at 0.1β1.5 ΞΌg/ml, DNA synthesis in MM253 appeared to be enhanced.
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