| Literature DB >> 23498847 |
Mario Leonardo Squadrito1, Martin Etzrodt, Michele De Palma, Mikael J Pittet.
Abstract
Deregulation of microRNAs (miRNAs) can drive oncogenesis, tumor progression, and metastasis by acting cell-autonomously in cancer cells. However, solid tumors are also infiltrated by large amounts of non-neoplastic stromal cells, including macrophages, which express several active miRNAs. Tumor-associated macrophages (TAMs) enhance angiogenic, immunosuppressive, invasive, and metastatic programming of neoplastic tissue and reduce host survival. Here, we review the role of miRNAs (including miR-155, miR-146, and miR-511) in the control of macrophage production and activation, and examine whether reprogramming miRNA activity in TAMs and/or their precursors might be effective for controlling tumor progression.Entities:
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Year: 2013 PMID: 23498847 PMCID: PMC3700601 DOI: 10.1016/j.it.2013.02.003
Source DB: PubMed Journal: Trends Immunol ISSN: 1471-4906 Impact factor: 16.687