Cell Reports
Volume 7, Issue 3, 8 May 2014, Pages 747-761
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Article
Regulated Splicing of the α6 Integrin Cytoplasmic Domain Determines the Fate of Breast Cancer Stem Cells

https://doi.org/10.1016/j.celrep.2014.03.059Get rights and content
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Highlights

  • The α6Aβ1 integrin splice variant promotes self-renewal and tumor initiation

  • The α6Aβ1 variant is unable to promote CSC function

  • Autocrine VEGF signaling regulates splicing of the α6 mRNA to generate α6B

  • VEGF regulates BMI-1 to repress expression of the splicing protein ESRP1

Summary

Although the α6β1 integrin has been implicated in the function of breast and other cancer stem cells (CSCs), little is known about its regulation and relationship to mechanisms involved in the genesis of CSCs. We report that a CD44high/CD24low population, enriched for CSCs, is comprised of distinct epithelial and mesenchymal populations that differ in expression of the two α6 cytoplasmic domain splice variants: α6A and α6B. α6Bβ1 expression defines the mesenchymal population and is necessary for CSC function, a function that cannot be executed by α6A integrins. The generation of α6Bβ1 is tightly controlled and occurs as a consequence of an autocrine vascular endothelial growth factor (VEGF) signaling that culminates in the transcriptional repression of a key RNA-splicing factor. These data alter our understanding of how α6β1 contributes to breast cancer, and they resolve ambiguities regarding the use of total α6 (CD49f) expression as a biomarker for CSCs.

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This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).