<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Jiang M</submitter><funding>Outstanding Young and Middle-aged Backbone Talents Project from Jilin Province Department of Finance</funding><funding>Natural Science Foundation Project from Jilin Provincial Department of Science and Technology</funding><funding>Bethune Planned Research project from Jilin University</funding><funding>Natural Science Foundation Project from Department of Science &amp;amp; Technology of Liaoning Province</funding><pagination>3473</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9655729</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(21)</volume><pubmed_abstract>M1 phenotype macrophages have anticancer characteristics, whereas M2 phenotype macrophages promote tumor growth and metastasis. A higher M1/M2 ratio, therefore, has a beneficial effect on the tumor immune microenvironment, thereby inhibiting tumor growth. The natural alkaloid curcumin is found to have anticancer properties. However, the mechanism remains unclear. In this study, a cell co-culture system and M2 macrophage model were used to evaluate the effects of curcumin on tumor-associated macrophage (TAM) phenotypes. Our results demonstrate that curcumin reprogrammed the M2 macrophages by reducing the level of anti-inflammatory cytokines (TGF-β, Arg-1, and IL-10) and an M2 surface marker (CD206) induced by Cal27 cells or IL-4, as well as upregulating proinflammatory cytokines (TNF-α, iNO</pubmed_abstract><journal>Cells</journal><pubmed_title>Curcumin Reprograms TAMs from a Protumor Phenotype towards an Antitumor Phenotype via Inhibiting MAO-A/STAT6 Pathway.</pubmed_title><pmcid>PMC9655729</pmcid><funding_grant_id>20200201329JC</funding_grant_id><funding_grant_id>2021-MS-175</funding_grant_id><funding_grant_id>JCSZ2019378-14</funding_grant_id><funding_grant_id>2018B27</funding_grant_id><pubmed_authors>Huang W</pubmed_authors><pubmed_authors>Qi Y</pubmed_authors><pubmed_authors>Lin Y</pubmed_authors><pubmed_authors>Li B</pubmed_authors><pubmed_authors>Jiang M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Curcumin Reprograms TAMs from a Protumor Phenotype towards an Antitumor Phenotype via Inhibiting MAO-A/STAT6 Pathway.</name><description>M1 phenotype macrophages have anticancer characteristics, whereas M2 phenotype macrophages promote tumor growth and metastasis. A higher M1/M2 ratio, therefore, has a beneficial effect on the tumor immune microenvironment, thereby inhibiting tumor growth. The natural alkaloid curcumin is found to have anticancer properties. However, the mechanism remains unclear. In this study, a cell co-culture system and M2 macrophage model were used to evaluate the effects of curcumin on tumor-associated macrophage (TAM) phenotypes. Our results demonstrate that curcumin reprogrammed the M2 macrophages by reducing the level of anti-inflammatory cytokines (TGF-β, Arg-1, and IL-10) and an M2 surface marker (CD206) induced by Cal27 cells or IL-4, as well as upregulating proinflammatory cytokines (TNF-α, iNO</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-19T06:38:18.738Z</modification><creation>2025-04-19T06:38:18.738Z</creation></dates><accession>S-EPMC9655729</accession><cross_references><pubmed>36359867</pubmed><doi>10.3390/cells11213473</doi></cross_references></HashMap>