| Literature DB >> 18328420 |
Marco Seandel1, Jason Butler, David Lyden, Shahin Rafii.
Abstract
Small numbers of proangiogenic bone marrow-derived cells (BMDCs) can play pivotal roles in tumor progression. In this issue of Cancer Cell, two papers, utilizing different tumor angiogenesis models, both find that activated MMP-9 delivered by BMDCs modulates neovessel remodeling, thereby promoting tumor growth. The changes in microvascular anatomy induced by MMP-9-expressing BMDCs are strikingly different between the preirradiated tumor vascular bed model employed by Ahn and Brown and the invasive glioblastoma model utilized by Du et al., likely mirroring the complexity of the real tumor microenvironment and the intricacy of roles of different BMDC populations in mediating tumor neoangiogenesis.Entities:
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Year: 2008 PMID: 18328420 PMCID: PMC2951026 DOI: 10.1016/j.ccr.2008.02.016
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743