Cancer Treatment Reviews
Volume 36, Issue 6 , Pages 485-491, October 2010

Molecular biology of breast cancer stem cells: Potential clinical applications

  • Nam P. Nguyen

      Affiliations

    • Department of Radiation Oncology, University of Arizona, N. Campbell Ave, Tucson, AZ 85724-5081, USA
    • Corresponding Author InformationCorresponding author. Tel.: +1 520 694 7236; fax: +1 520 626 2032.
  • ,
  • Fabio S. Almeida

      Affiliations

    • Division of Nuclear Medicine, AZ, USA
  • ,
  • Alex Chi

      Affiliations

    • Department of Radiation Oncology, University of Arizona, N. Campbell Ave, Tucson, AZ 85724-5081, USA
  • ,
  • Ly M. Nguyen

      Affiliations

    • The School of Public Health, University of Michigan, Ann Arbor, MI, USA
  • ,
  • Deirdre Cohen

      Affiliations

    • Department of Radiation Oncology, University of Arizona, N. Campbell Ave, Tucson, AZ 85724-5081, USA
  • ,
  • Ulf Karlsson

      Affiliations

    • Department of Radiation Oncology, Marshfield Clinic, Marshfield, WI, USA
  • ,
  • Vincent Vinh-Hung

      Affiliations

    • Department of Radiation Oncology, University of Geneva, Geneva, Switzerland

Received 22 November 2009; received in revised form 7 February 2010; accepted 13 February 2010. published online 15 March 2010.

Summary 

Breast cancer stem cells (CSC) have been postulated recently as responsible for failure of breast cancer treatment. The purpose of this study is to review breast CSCs molecular biology with respect to their mechanism of resistance to conventional therapy, and to develop treatment strategies that may improve survival of breast cancer patients. A literature search has identified in vitro and in vivo studies of breast CSCs. Breast CSCs overexpress breast cancer resistance protein (BCRP) which allows cancer cells to transport actively chemotherapy agents out of the cells. Radioresistance is modulated through activation of Wnt signaling pathway and overexpression of genes coding for glutathione. Lapatinib can selectively target HER-2 positive breast CSCs and improves disease-free survival in these patients. Metformin may target basal type breast CSCs. Parthenolide and oncolytic viruses are promising targeting agents for breast CSCs. Future clinical trials for breast cancer should include anti-cancer stem cells targeting agents in addition to conventional chemotherapy. Hypofractionation radiotherapy may be indicated for residual disease post chemotherapy.

Keywords: Breast cancer stem cells, Chemoresistance, Radioresistance

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PII: S0305-7372(10)00037-X

doi:10.1016/j.ctrv.2010.02.016

Cancer Treatment Reviews
Volume 36, Issue 6 , Pages 485-491, October 2010