Toggle Main Menu Toggle Search

Open Access padlockePrints

Cancer Stem Cells and Side Population Cells in Breast Cancer and Metastasis

Lookup NU author(s): Dr Kelly Britton, Emeritus Professor John Kirby, Professor Thomas Lennard, Dr Annette Meeson


Full text for this publication is not currently held within this repository. Alternative links are provided below where available.


Abstract: In breast cancer it is never the primary tumour that is fatal; instead it is the development of metastatic disease which is the major cause of cancer related mortality. There is accumulating evidence that suggests that Cancer Stem Cells (CSC) may play a role in breast cancer development and progression. Breast cancer stem cell populations, including side population cells (SP), have been shown to be primitive stem cell-like populations, being long-lived, self-renewing and highly proliferative. SP cells are identified using dual wavelength flow cytometry combined with Hoechst 33342 dye efflux, this ability is due to expression of one or more members of the ABC transporter family. They have increased resistance to chemotherapeutic agents and apoptotic stimuli and have increased migratory potential above that of the bulk tumour cells making them strong candidates for the metastatic spread of breast cancer. Treatment of nearly all cancers usually involves one first-line agent known to be a substrate of an ABC transporter thereby increasing the risk of developing drug resistant tumours. At present there is no marker available to identify SP cells using immunohistochemistry on breast cancer patient samples. If SP cells do play a role in breast cancer progression/Metastatic Breast Cancer (MBC), combining chemotherapy with ABC inhibitors may be able to destroy both the cells making up the bulk tumour and the cancer stem cell population thus preventing the risk of drug resistant disease, recurrence or metastasis.

Publication metadata

Author(s): Britton KM, Kirby JA, Lennard TWJ, Meeson AP

Publication type: Review

Publication status: Published

Journal: Cancers

Year: 2011

Volume: 3

Issue: 2

Pages: 2106-2130

Print publication date: 19/04/2011

ISSN (print): 2072-6694


DOI: 10.3390/cancers3022106