4.5 Article

Tumor Cell-Derived Periostin Regulates Cytokines That Maintain Breast Cancer Stem Cells

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MOLECULAR CANCER RESEARCH
卷 14, 期 1, 页码 103-113

出版社

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/1541-7786.MCR-15-0079

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资金

  1. Susan G. Komen for the Cure [KG081435]
  2. NIH/NCI [CA165707, CA138509]
  3. Department of Defense, Breast Cancer Research Program [W81XWH-11-1-006]
  4. Research Promotion Foundation, Cyprus [DIDAKTOR/0609/24]
  5. Boston University Genome Science Institute
  6. Boston University Flow Cytometry Core Facility
  7. Boston University Clinical and Translational Science Institute (CTSA) [UL1TR000157]

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Basal-like breast cancer (BLBC) is an aggressive subtype of breast cancer which is often enriched with cancer stem cells (CSC), but the underlying molecular basis for this connection remains elusive. We hypothesized that BLBC cells are able to establish a niche permissive to the maintenance of CSCs and found that tumor cell-derived periostin (POSTN), a component of the extracellular matrix, as well as a corresponding cognate receptor, integrin alpha(v)beta(3), are highly expressed in a subset of BLBC cell lines as well as in CSC-enriched populations. Furthermore, we demonstrated that an intact periostin-integrin beta 3 signaling axis is required for the maintenance of breast CSCs. POSTN activates the ERK signaling pathway and regulates NF-kappa B-mediated transcription of key cytokines, namely IL6 and IL8, which in turn control downstream activation of STAT3. In summary, these findings suggest that BLBC cells have an innate ability to establish a microenvironmental niche supportive of CSCs. (C) 2015 AACR.

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