Cisplatin-resistant derivatives of murine L1210 leukemia cells are not susceptible to growth-inhibiting and apoptosis-inducing actions of transforming growth factor-beta1. |
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Authors: | R S Stoika Yakymovych" target="_blank">I A Yakymovych MYaYakymovych V F Chekhun |
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Institution: | Division of Regulatory Cell Systems, Institute of Biochemistry, National Academy of Sciences of Ukraine, Lviv. stoika@biochem.lviv.ua |
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Abstract: | Murine L1210 leukemia cells possessing an increased resistance to cisplatin were found to be refractory to transforming growth factor (TGF)-beta1-induced growth inhibition, while the parental L1210 cells were strongly inhibited by this cytokine. Growth inhibition was estimated on the basis of 3H]thymidine incorporation, cell counting and colony-forming assay. Cisplatin-resistant L1210 cells were also shown to be much more resistant than the parental cells to both cisplatin- and TGF-beta1-induced apoptosis. These results suggest the existence of cross-resistance to cisplatin and TGF-beta1 in the studied leukemia cells. |
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