Human breast cancer MCF-7 cell line contains inherently drug-resistant subclones with distinct genotypic and phenotypic features

Int J Oncol. 2002 May;20(5):913-20.

Abstract

The resistance of cancer cells to multiple chemotherapeutic agents poses a major problem in the successful treatment of breast cancer. Whether drug resistance is due to changes induced in the drug-exposed tumor cells or represents the selective growth of one or more drug-resistant clones present in the initial tumor remains controversial. Here we provide evidence that the development of multidrug resistance in a human breast cancer cell line (MCF-7) is a result of propagation of an inherently resistant subclone. The drug-resistant MCF-7 (MCF-7/DOX) cells exhibited several phenotypic and genotypic features that were notably distinct from those observed in the parental drug-sensitive (MCF-7/WT) cells. The most striking change was the presence of a full-length functional caspase-3 in MCF-7/DOX cells that was missing in the parental MCF-7/WT cells due to a deletion mutation in the caspase-3 gene. A drug-resistant MCF-7 cell subline (MCF-7/WT/DOX) was established by exposing the MCF-7/WT cells directly to a high dose of doxorubicin and used for determining the phenotypic and genotypic alterations associated with drug resistance. The MCF-7/WT/DOX cells exhibited alterations identical to those of the MCF-7/DOX cells but which were strikingly distinct from the parental MCF-7/WT cell line. These results suggest that drug resistance is an inherent property of some cancer cells that are present in the initial tumor burden and exhibit distinct phenotypic/genotypic alterations.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Breast Neoplasms / drug therapy
  • Breast Neoplasms / metabolism*
  • Caspase 3
  • Caspases / biosynthesis
  • Chromosome Banding
  • Chromosomes / ultrastructure
  • Dose-Response Relationship, Drug
  • Drug Resistance, Neoplasm*
  • Enzyme Inhibitors / pharmacology
  • Genotype
  • Humans
  • Immunohistochemistry
  • Karyotyping
  • Phenotype
  • Reverse Transcriptase Polymerase Chain Reaction
  • Staurosporine / pharmacology
  • Time Factors
  • Tumor Cells, Cultured

Substances

  • Enzyme Inhibitors
  • CASP3 protein, human
  • Caspase 3
  • Caspases
  • Staurosporine