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Loss of microRNA-27b-mediated gene repression promotes the generation of breast cancer stem cells
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Molecular and Genetic Medicine

ISSN: 1747-0862

Open Access

Loss of microRNA-27b-mediated gene repression promotes the generation of breast cancer stem cells


International Conference and Exhibition on Molecular Medicine and Diagnostics

August 24-26, 2015 London, UK

Ryou-u Takahashi, Hiroaki Miyazaki and Takahiro Ochiya

Scientific Tracks Abstracts: J Mol Genet Med

Abstract :

Accumulating lines of evidence suggest that the key property that distinguishes cancer stem cells (CSCs) from non-CSCs is the
ability to create their abnormal niche that remains in a dormant and tolerant state under stressful exposures such as conventional
chemotherapy and radiotherapy. However, the molecular mechanisms for the generation of CSC niche remain elusive. In this study,
we show that microRNA-27b (miR-27b) plays important roles in the generation of breast CSCs (BCSCs).The down-regulation of
miR-27b was essential for the generation of BCSCs that show the self-renewal, drug tolerant and high tumorigenic activities. Further
analysis revealed that miR-27b overexpression inhibited the drug-resistance and tumor seeding ability of breast cancer cells via
suppressing the non-CSC to CSC transition under stressful exposures. Therefore, these findings elucidate a new molecular mechanism
for the generation of BCSCs and suggest that modulating miR-27b with conventional anticancer treatments might be a promising
approach to overcome BCSCs.

Biography :

Ryou-u Takahashi is a Staff Scientist of Division of Molecular and Cellular Medicine at the National Cancer Center Research Institute, Tokyo. After he got a PhD in 2008 in
Tokyo Institute of Technology, he went on to do a Post-doc at the National Cancer Center Research Institute. He focuses the development of novel animal models, methods
and strategies to study the molecular mechanisms for the acquisition of CSC properties; especially the current focus is siRNA- and miRNA-based therapy against CSCs.

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Citations: 3919

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