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Taxol resistant mutants of Chinese hamster ovary cells: Genetic biochemical, and cross‐resistance studies
Author(s) -
Gupta Radhey S.
Publication year - 1983
Publication title -
journal of cellular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 174
eISSN - 1097-4652
pISSN - 0021-9541
DOI - 10.1002/jcp.1041140122
Subject(s) - colcemid , chinese hamster ovary cell , mutant , biology , puromycin , podophyllotoxin , vinblastine , microtubule , microbiology and biotechnology , cell culture , biochemistry , genetics , chemistry , protein biosynthesis , gene , chemotherapy , stereochemistry
The effects of the microtubule inhibitor taxol on the growth and viability of Chinese hamster ovary (CHO) cells have been examined. Stable mutants which are between seven to 11‐fold more resistant to taxol have been selected in a single step from ethyl methanesulfonate‐mutagenized CHO cells. The two taxol‐resistant mutants (Tax R ‐1 and Tax R ‐2) which have been studied in detail exhibit novel and strikingly different cross‐resistance/collateral sensitivity patterns to various microtubule inhibitors. For example, the Tax R ‐1 mutant exhibits increased resistance to vinblastine, but in comparison to the parental cells, it shows enhanced sensitivity toward colchicine, colcemid, stegnacine, and griseofulvin. However, the sensitivity of this mutant toward other unrelated compounds, e.g., puromycin, daunomycin, etc., remained largely unaltered. The specific pattern of cross‐resistance/collateral‐sensitivity of this mutant toward various microtubule inhibitors suggests that the genetic lesion in this mutant may be affecting a microtubule‐related component. The Tax R ‐2 mutant, in contrast, is highly resistant to various microtubule inhibitors including colchicine, colcemid, stegnacine, maytan‐sine, vinblastine, and podophyllotoxin. This mutant also exhibits greatly increased cross‐resistance to daunomycin, puromycin, ethidium bromide, and VM‐26 (compounds which do not inhibit microtubule assembly), and shows reduced cellular uptake of 3 H‐daunomycin indicating that the genetic lesion in this mutant nonspecifically affects the membrane permeability of various drugs. The cell hybrids formed between Tax R ‐1 (or Tax R ‐2 mutant(s)) and a taxol‐sensitive cell line exhibit intermediate levels of resistance to the drug, indicating that the Tax R phenotypes of both these mutants behave codominantly under these conditions.