<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>22(2)</volume><submitter>Weng TY</submitter><pubmed_abstract>Induction of thrombospondin 1 (TSP-1) is generally assumed to suppress tumor growth through inhibiting angiogenesis; however, it is less clear how TSP-1 in dendritic cells (DCs) influences tumor progression. We investigated tumor growth and immune mechanism by downregulation of TSP-1 in dendritic cells. Administration of TSP-1 small hairpin RNA (shRNA) through the skin produced anticancer therapeutic effects. Tumor-infiltrating CD4(+) and CD8(+) T cells were increased after the administration of TSP-1 shRNA. The expression of interleukin-12 and interferon-γ in the lymph nodes was enhanced by injection of TSP-1 shRNA. Lymphocytes from the mice injected with TSP-1 shRNA selectively killed the tumor cells, and the cytotoxicity of lymphocytes was abolished by depletion of CD8(+) T cells. Injec</pubmed_abstract><journal>Molecular therapy : the journal of the American Society of Gene Therapy</journal><pagination>292-302</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3918914</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A novel cancer therapeutic using thrombospondin 1 in dendritic cells.</pubmed_title><pmcid>PMC3918914</pmcid><pubmed_authors>Chang JY</pubmed_authors><pubmed_authors>Huang SS</pubmed_authors><pubmed_authors>Wang CY</pubmed_authors><pubmed_authors>Lin CM</pubmed_authors><pubmed_authors>Lai MD</pubmed_authors><pubmed_authors>Yen MC</pubmed_authors><pubmed_authors>Lin CC</pubmed_authors><pubmed_authors>Chen WC</pubmed_authors><pubmed_authors>Weng TY</pubmed_authors><pubmed_authors>Chen YL</pubmed_authors></additional><is_claimable>false</is_claimable><name>A novel cancer therapeutic using thrombospondin 1 in dendritic cells.</name><description>Induction of thrombospondin 1 (TSP-1) is generally assumed to suppress tumor growth through inhibiting angiogenesis; however, it is less clear how TSP-1 in dendritic cells (DCs) influences tumor progression. We investigated tumor growth and immune mechanism by downregulation of TSP-1 in dendritic cells. Administration of TSP-1 small hairpin RNA (shRNA) through the skin produced anticancer therapeutic effects. Tumor-infiltrating CD4(+) and CD8(+) T cells were increased after the administration of TSP-1 shRNA. The expression of interleukin-12 and interferon-γ in the lymph nodes was enhanced by injection of TSP-1 shRNA. Lymphocytes from the mice injected with TSP-1 shRNA selectively killed the tumor cells, and the cytotoxicity of lymphocytes was abolished by depletion of CD8(+) T cells. Injec</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Feb</publication><modification>2026-04-29T22:36:41.379Z</modification><creation>2019-03-27T01:21:30Z</creation></dates><accession>S-EPMC3918914</accession><cross_references><pubmed>24127010</pubmed><doi>10.1038/mt.2013.236</doi></cross_references></HashMap>