<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>29(3)</volume><submitter>Yang Y</submitter><funding>National Natural Science Foundation of China</funding><pubmed_abstract>Pancreatic ductal adenocarcinoma (PDAC), one of the most aggressive tumors all over the world, has a generally poor prognosis, and its progression is positively correlated with the density of blood vessels. Recently, tumor-associated macrophages (TAMs) were proven to be beneficial for angiogenesis, but their mechanism of action remains unclear. Our study indicated that M2 macrophages were positively correlated with the microvessel density (MVD) of PDAC tissues, and M2 macrophage-derived exosomes (MDEs) could promote the angiogenesis of mouse aortic endothelial cells (MAECs) in vitro. At the same time, the M2 MDEs could also promote the growth of subcutaneous tumors and increase the vascular density of mice. Moreover, we also found that miR-155-5p and miR-221-5p levels in the M2 MDEs were h</pubmed_abstract><journal>Molecular therapy : the journal of the American Society of Gene Therapy</journal><pagination>1226-1238</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7934635</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>M2 Macrophage-Derived Exosomes Promote Angiogenesis and Growth of Pancreatic Ductal Adenocarcinoma by Targeting E2F2.</pubmed_title><pmcid>PMC7934635</pmcid><pubmed_authors>Huang C</pubmed_authors><pubmed_authors>Cao M</pubmed_authors><pubmed_authors>Guo Z</pubmed_authors><pubmed_authors>Zhang K</pubmed_authors><pubmed_authors>Cao J</pubmed_authors><pubmed_authors>Han X</pubmed_authors><pubmed_authors>Qiu Z</pubmed_authors><pubmed_authors>Yang Y</pubmed_authors><pubmed_authors>Teng B</pubmed_authors><pubmed_authors>Chen W</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Wu W</pubmed_authors><pubmed_authors>Cao P</pubmed_authors></additional><is_claimable>false</is_claimable><name>M2 Macrophage-Derived Exosomes Promote Angiogenesis and Growth of Pancreatic Ductal Adenocarcinoma by Targeting E2F2.</name><description>Pancreatic ductal adenocarcinoma (PDAC), one of the most aggressive tumors all over the world, has a generally poor prognosis, and its progression is positively correlated with the density of blood vessels. Recently, tumor-associated macrophages (TAMs) were proven to be beneficial for angiogenesis, but their mechanism of action remains unclear. Our study indicated that M2 macrophages were positively correlated with the microvessel density (MVD) of PDAC tissues, and M2 macrophage-derived exosomes (MDEs) could promote the angiogenesis of mouse aortic endothelial cells (MAECs) in vitro. At the same time, the M2 MDEs could also promote the growth of subcutaneous tumors and increase the vascular density of mice. Moreover, we also found that miR-155-5p and miR-221-5p levels in the M2 MDEs were h</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Mar</publication><modification>2025-04-18T20:06:09.38Z</modification><creation>2025-04-07T07:54:14.711Z</creation></dates><accession>S-EPMC7934635</accession><cross_references><pubmed>33221435</pubmed><doi>10.1016/j.ymthe.2020.11.024</doi></cross_references></HashMap>