Literature DB >> 26955842

Breast cancer stem cells programs: enter the (non)-code.

Marion A Salvador, Daniel Birnbaum, Emmanuelle Charafe-Jauffret, Christophe Ginestier.   

Abstract

Breast tumors exhibit a hierarchical cellular organization driven by several subpopulations of cancer stem cells (CSCs). These breast CSC subpopulations are able to infinitely self-renew and to differentiate, giving rise to tumor heterogeneity. Accumulating evidence show that breast CSCs resist conventional therapies and i`nitiate tumor relapse. The development of anti-CSCs therapies may therefore greatly improve patient survival. A better elucidation of molecular circuitries involved in stemness would offer new relevant targets. Noncoding RNAs, especially microRNAs and long noncoding RNAs, are regulators of cell identity and are notably found deregulated in breast CSCs. This review will focus on noncoding RNAs involved in CSCs biology during breast cancer initiation, maintenance, therapeutic resistance and metastatic progression. Potential clinical applications using noncoding RNAs as biomarkers or therapies will be discussed.
© The Author 2016. Published by Oxford University Press. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Entities:  

Keywords:  RNA; breast; cancer; cancer stem cell; epigenetics; long; microRNA; noncoding

Mesh:

Substances:

Year:  2016        PMID: 26955842     DOI: 10.1093/bfgp/elw003

Source DB:  PubMed          Journal:  Brief Funct Genomics        ISSN: 2041-2649            Impact factor:   4.241


  2 in total

1.  Flick the cancer stem cells' switch to turn cancer off.

Authors:  Christophe Ginestier; Daniel Birnbaum; Emmanuelle Charafe-Jauffret
Journal:  Mol Cell Oncol       Date:  2017-04-28

Review 2.  Alterations of cell cycle genes in cancer: unmasking the role of cancer stem cells.

Authors:  Hasan Onur Caglar; Cigir Biray Avci
Journal:  Mol Biol Rep       Date:  2020-02-28       Impact factor: 2.316

  2 in total

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