<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Choi J</submitter><funding>NIBIB NIH HHS</funding><funding>NCATS NIH HHS</funding><funding>NCI NIH HHS</funding><pubmed_abstract>Autophagy is known to suppress tumor initiation by removing genotoxic stresses in normal cells. Conversely, autophagy is also known to support tumor progression by alleviating metabolic stresses in neoplastic cells. Centered on this pro-tumor role of autophagy, there have been many clinical trials to treat cancers through systemic blocking of autophagy. Such systemic inhibition affects both tumor cells and non-tumor cells, and the consequence of blocked autophagy in non-tumor cells in the context of tumor microenvironment is relatively understudied. Here, we examined the effect of autophagy-deficient myeloid cells on the progression of autophagy-competent tumors. We found that blocking autophagy only in myeloid cells modulated tumor progression markedly but such effects were context depend</pubmed_abstract><journal>bioRxiv : the preprint server for biology</journal><pagination>2024.07.12.603292</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11275940</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Context-dependent roles for autophagy in myeloid cells in tumor progression.</pubmed_title><pmcid>PMC11275940</pmcid><funding_grant_id>DP2 CA225208</funding_grant_id><funding_grant_id>R01 CA232419</funding_grant_id><funding_grant_id>UL1 TR000430</funding_grant_id><funding_grant_id>K99 EB022636</funding_grant_id><funding_grant_id>R01 CA199663</funding_grant_id><funding_grant_id>R00 EB022636</funding_grant_id><funding_grant_id>P30 CA014599</funding_grant_id><pubmed_authors>Macleod KF</pubmed_authors><pubmed_authors>Park G</pubmed_authors><pubmed_authors>Becker L</pubmed_authors><pubmed_authors>Hwang S</pubmed_authors><pubmed_authors>Lee SS</pubmed_authors><pubmed_authors>Dominici E</pubmed_authors><pubmed_authors>Choi J</pubmed_authors><pubmed_authors>Kron SJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Context-dependent roles for autophagy in myeloid cells in tumor progression.</name><description>Autophagy is known to suppress tumor initiation by removing genotoxic stresses in normal cells. Conversely, autophagy is also known to support tumor progression by alleviating metabolic stresses in neoplastic cells. Centered on this pro-tumor role of autophagy, there have been many clinical trials to treat cancers through systemic blocking of autophagy. Such systemic inhibition affects both tumor cells and non-tumor cells, and the consequence of blocked autophagy in non-tumor cells in the context of tumor microenvironment is relatively understudied. Here, we examined the effect of autophagy-deficient myeloid cells on the progression of autophagy-competent tumors. We found that blocking autophagy only in myeloid cells modulated tumor progression markedly but such effects were context depend</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jul</publication><modification>2026-04-14T03:11:46.99Z</modification><creation>2025-04-06T14:23:11.817Z</creation></dates><accession>S-EPMC11275940</accession><cross_references><pubmed>39071306</pubmed><doi>10.1101/2024.07.12.603292</doi></cross_references></HashMap>