| Literature DB >> 22624717 |
Myron S Ignatius1, Eleanor Chen2, Natalie M Elpek3, Adam Z Fuller1, Inês M Tenente4, Ryan Clagg1, Sali Liu1, Jessica S Blackburn1, Corinne M Linardic5, Andrew E Rosenberg6, Petur G Nielsen6, Thorsten R Mempel3, David M Langenau7.
Abstract
Embryonal rhabdomyosarcoma (ERMS) is an aggressive pediatric sarcoma of muscle. Here, we show that ERMS-propagating potential is confined to myf5+ cells and can be visualized in live, fluorescent transgenic zebrafish. During early tumor growth, myf5+ ERMS cells reside adjacent normal muscle fibers. By late-stage ERMS, myf5+ cells are reorganized into distinct regions separated from differentiated tumor cells. Time-lapse imaging of late-stage ERMS revealed that myf5+ cells populate newly formed tumor only after seeding by highly migratory myogenin+ ERMS cells. Moreover, myogenin+ ERMS cells can enter the vasculature, whereas myf5+ ERMS-propagating cells do not. Our data suggest that non-tumor-propagating cells likely have important supportive roles in cancer progression and facilitate metastasis.Entities:
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Year: 2012 PMID: 22624717 PMCID: PMC3381357 DOI: 10.1016/j.ccr.2012.03.043
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743