<HashMap><database>biostudies-literature</database><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>39</viewCount><searchCount>0</searchCount></scores><additional><omics_type>Unknown</omics_type><volume>19(1)</volume><submitter>Xue T</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>This study aimed to explore the prognostic significance of tumor-associated macrophage (TAM) infiltration in colorectal cancer (CRC) patients.&lt;h4>Methods&lt;/h4>Tissue microarray and immunohistochemistry were used to detect the infiltration of CD163+ TAMs in 209 CRC samples, and the Kaplan-Meier method was used for survival analysis. Cox proportional hazards analysis was used for univariate analysis and multivariate analysis of clinically relevant confounders.&lt;h4>Results&lt;/h4>The samples were divided into low-level (n = 105) and high-level infiltration groups (n = 104) by the median number of CD163+ TAMs detected. The overall survival (OS) and disease-free survival (DFS) of CRC patients in the low-level CD163+ TAM infiltration group were longer than those in the high-level CD163+ TAM infiltration group (P &lt; 0.001). Infiltration of CD163+ TAMs in CRC tissues was a negative prognostic factor for CRC patients. Risks of death and disease recurrence for CRC patients in the low-level CD163+ TAM infiltration group were lower than those in the high-level CD163+ TAM infiltration group (HR&lt;sub>OS&lt;/sub> = 0.183, 95% CI 0.052-0.647, P = 0.008; HR&lt;sub>DFS&lt;/sub> = 0.191, 95% CI 0.078-0.470, P = 0.000).&lt;h4>Conclusions&lt;/h4>The infiltration of CD163+ TAMs in CRC tissue is an independent adverse factor for the prognosis of CRC patients. High-level infiltration of CD163+ TAMs is associated with shorter OS and DFS.</pubmed_abstract><journal>World journal of surgical oncology</journal><pagination>186</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8229299</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Prognostic significance of CD163+ tumor-associated macrophages in colorectal cancer.</pubmed_title><pmcid>PMC8229299</pmcid><pubmed_authors>Xue T</pubmed_authors><pubmed_authors>Yan K</pubmed_authors><pubmed_authors>Chen Z</pubmed_authors><pubmed_authors>Cai Y</pubmed_authors><pubmed_authors>Chen X</pubmed_authors><pubmed_authors>Wu W</pubmed_authors><pubmed_authors>Sun J</pubmed_authors><view_count>39</view_count></additional><is_claimable>false</is_claimable><name>Prognostic significance of CD163+ tumor-associated macrophages in colorectal cancer.</name><description>&lt;h4>Background&lt;/h4>This study aimed to explore the prognostic significance of tumor-associated macrophage (TAM) infiltration in colorectal cancer (CRC) patients.&lt;h4>Methods&lt;/h4>Tissue microarray and immunohistochemistry were used to detect the infiltration of CD163+ TAMs in 209 CRC samples, and the Kaplan-Meier method was used for survival analysis. Cox proportional hazards analysis was used for univariate analysis and multivariate analysis of clinically relevant confounders.&lt;h4>Results&lt;/h4>The samples were divided into low-level (n = 105) and high-level infiltration groups (n = 104) by the median number of CD163+ TAMs detected. The overall survival (OS) and disease-free survival (DFS) of CRC patients in the low-level CD163+ TAM infiltration group were longer than those in the high-level CD163+ TAM infiltration group (P &lt; 0.001). Infiltration of CD163+ TAMs in CRC tissues was a negative prognostic factor for CRC patients. Risks of death and disease recurrence for CRC patients in the low-level CD163+ TAM infiltration group were lower than those in the high-level CD163+ TAM infiltration group (HR&lt;sub>OS&lt;/sub> = 0.183, 95% CI 0.052-0.647, P = 0.008; HR&lt;sub>DFS&lt;/sub> = 0.191, 95% CI 0.078-0.470, P = 0.000).&lt;h4>Conclusions&lt;/h4>The infiltration of CD163+ TAMs in CRC tissue is an independent adverse factor for the prognosis of CRC patients. High-level infiltration of CD163+ TAMs is associated with shorter OS and DFS.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Jun</publication><modification>2024-12-03T22:41:40.43Z</modification><creation>2022-02-10T17:17:35.8Z</creation></dates><accession>S-EPMC8229299</accession><cross_references><pubmed>34167561</pubmed><doi>10.1186/s12957-021-02299-y</doi></cross_references></HashMap>