Stem Cell Models for Breast and Colon Cancer: Experimental Approach for Drug Discovery

Int J Mol Sci. 2022 Aug 17;23(16):9223. doi: 10.3390/ijms23169223.

Abstract

The progression of the early stages of female breast and colon cancer to metastatic disease represents a major cause of mortality in women. Multi-drug chemotherapy and/or pathway selective targeted therapy are notable for their off-target effects and are associated with spontaneous and/or acquired chemotherapy resistance and the emergence of premalignant chemo-resistant cancer-initiating stem cells. The stem cell populations are responsible for the evolution of therapy-resistant metastatic disease. These limitations emphasize an unmet need to develop reliable drug-resistant cancer stem cell models as novel experimental approaches for therapeutic alternatives in drug discovery platforms. Drug-resistant stem cell models for breast and colon cancer subtypes exhibit progressive growth in the presence of cytotoxic chemo-endocrine therapeutics. The resistant cells exhibit upregulated expressions of stem cell-selective cellular and molecular markers. Dietary phytochemicals, nutritional herbs and their constituent bioactive compounds have documented growth inhibitory efficacy for cancer stem cells. The mechanistic leads for the stem cell-targeted efficacy of naturally occurring agents validates the present experimental approaches for new drug discovery as therapeutic alternatives for therapy-resistant breast and colon cancer. The present review provides a systematic discussion of published evidence on (i) conventional/targeted therapy for breast and colon cancer, (ii) cellular and molecular characterization of stem cell models and (iii) validation of the stem cell models as an experimental approach for novel drug discovery of therapeutic alternatives for therapy-resistant cancers.

Keywords: breast and colon cancer; cancer stem cells; therapeutic alternatives.

Publication types

  • Review

MeSH terms

  • Breast / metabolism
  • Breast Neoplasms* / metabolism
  • Cell Line, Tumor
  • Colonic Neoplasms* / pathology
  • Drug Discovery
  • Drug Resistance, Neoplasm
  • Female
  • Humans
  • Neoplastic Stem Cells / metabolism

Grants and funding

This review received no extra-mural funding.