| Literature DB >> 28855213 |
Javier Figueroa1, Lynette M Phillips1, Tal Shahar1, Anwar Hossain1, Joy Gumin1, Hoon Kim2, Andrew J Bean3, George A Calin4, Juan Fueyo5, Edgar T Walters6, Raghu Kalluri7, Roel G Verhaak2, Frederick F Lang8.
Abstract
Tumor-stromal communications impact tumorigenesis in ways that are incompletely understood. Here, we show that glioma-associated human mesenchymal stem cells (GA-hMSC), a newly identified stromal component of glioblastoma, release exosomes that increase the proliferation and clonogenicity of tumor-initiating glioma stem-like cells (GSC). This event leads to a significantly greater tumor burden and decreased host survival compared with untreated GSCs in orthotopic xenografts. Analysis of the exosomal content identified miR-1587 as a mediator of the exosomal effects on GSCs, in part via downregulation of the tumor-suppressive nuclear receptor corepressor NCOR1. Our results illuminate the tumor-supporting role for GA-hMSCs by identifying GA-hMSC-derived exosomes in the intercellular transfer of specific miRNA that enhance the aggressiveness of glioblastoma. Cancer Res; 77(21); 5808-19. ©2017 AACR. ©2017 American Association for Cancer Research.Entities:
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Year: 2017 PMID: 28855213 PMCID: PMC5668150 DOI: 10.1158/0008-5472.CAN-16-2524
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701