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Cisplatin-resistant derivatives of murine L1210 leukemia cells are not susceptible to growth-inhibiting and apoptosis-inducing actions of transforming growth factor-beta1.

作者信息

Stoika R S, Yakymovych I A, Chekhun V F

机构信息

Division of Regulatory Cell Systems, Institute of Biochemistry, National Academy of Sciences of Ukraine, Lviv.

出版信息

Anticancer Drugs. 1999 Jun;10(5):457-63. doi: 10.1097/00001813-199906000-00005.

DOI:10.1097/00001813-199906000-00005
PMID:10477165
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.

摘要

相似文献

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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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[Cisplatin resistance in a murine leukemia cell line associated with defect of apoptosis].[与凋亡缺陷相关的小鼠白血病细胞系中的顺铂耐药性]
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