<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14(4)</volume><submitter>Cao H</submitter><pubmed_abstract>Tumor-associated macrophages (TAMs) are critical immune cells infiltrated into tumor. In present study, we evaluated the effects of Qi Ling (QL), a traditional Chinese medicine on paclitaxel resistance in prostate cancer cells and explored the underlying mechanisms. We administrated QL to rats and collected the serum from QL-treated rats (QL-serum). We established the co-culture system of TAMs/paclitaxel resistant prostate cancer cells. We treated the TAMs with QL-serum and measured the viability of paclitaxel resistant prostate cancer cells after exposing to paclitaxel. We monitored the expression of M1 and M2 markers, the expression and activation of IL-6/STAT3 signaling pathways in TAMs after QL treatment. We treated TAMs with QL-serum together with interleukin (IL)-6, measured the expr</pubmed_abstract><journal>Aging</journal><pagination>1812-1821</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8908933</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Qi Ling decreases paclitaxel resistance in the human prostate cancer by reversing tumor-associated macrophages function.</pubmed_title><pmcid>PMC8908933</pmcid><pubmed_authors>Gao R</pubmed_authors><pubmed_authors>Cao H</pubmed_authors><pubmed_authors>Wang D</pubmed_authors><pubmed_authors>Feng Y</pubmed_authors><pubmed_authors>Chen L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Qi Ling decreases paclitaxel resistance in the human prostate cancer by reversing tumor-associated macrophages function.</name><description>Tumor-associated macrophages (TAMs) are critical immune cells infiltrated into tumor. In present study, we evaluated the effects of Qi Ling (QL), a traditional Chinese medicine on paclitaxel resistance in prostate cancer cells and explored the underlying mechanisms. We administrated QL to rats and collected the serum from QL-treated rats (QL-serum). We established the co-culture system of TAMs/paclitaxel resistant prostate cancer cells. We treated the TAMs with QL-serum and measured the viability of paclitaxel resistant prostate cancer cells after exposing to paclitaxel. We monitored the expression of M1 and M2 markers, the expression and activation of IL-6/STAT3 signaling pathways in TAMs after QL treatment. We treated TAMs with QL-serum together with interleukin (IL)-6, measured the expr</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Feb</publication><modification>2025-04-26T04:49:22.766Z</modification><creation>2025-04-06T11:14:17.165Z</creation></dates><accession>S-EPMC8908933</accession><cross_references><pubmed>35193986</pubmed><doi>10.18632/aging.203904</doi></cross_references></HashMap>