<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhang X</submitter><funding>The Key Scientific Research Project of Colleges and Universities in Henan Province of China</funding><funding>Renshu Fund Project of Hunan Provincial People’s Hospital</funding><funding>Renshu Fund Project of Hunan Provincial People's Hospital</funding><funding>National Science and Technology Major Project of China under Grant</funding><funding>The Training Program of Henan Provincial Higher Vocational School Young Backbone Teachers</funding><funding>The Science and Technology Project in Henan Province of China</funding><funding>The Joint Construction Project of Henan Medical Science and Technology Research Plan in Henan Province of China</funding><pagination>393</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9733014</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>22(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>The dysregulation of CD5L has been reported in hepatocellular carcinoma (HCC). However, its functions in HCC were controversial. In this study, we aimed to identify CD5L-associated pathways and markers and explore their values in HCC diagnosis, prognosis and treatment.&lt;h4>Methods&lt;/h4>HCC datasets with gene expression profiles and clinical data in TCGA and ICGC were downloaded. The immune/stroma cell infiltrations were estimated with xCell. CD5L-associated pathways and CD5L-associated genes (CD5L-AGs) were identified with gene expression comparisons and gene set enrichment analysis (GSEA). Cox regression, Kaplan-Meier survival analysis, and least absolute shrinkage and selection operator (LASSO) regression analysis were performed. The correlations of the key genes with im</pubmed_abstract><journal>Cancer cell international</journal><pubmed_title>CD5L-associated gene analyses highlight the dysregulations, prognostic effects, immune associations, and drug-sensitivity predicative potentials of LCAT and CDC20 in hepatocellular carcinoma.</pubmed_title><pmcid>PMC9733014</pmcid><funding_grant_id>LHGJ20190717</funding_grant_id><funding_grant_id>20B320007</funding_grant_id><funding_grant_id>222102310408</funding_grant_id><funding_grant_id>2020-20</funding_grant_id><funding_grant_id>RS201803</funding_grant_id><funding_grant_id>2018ZX10302205</funding_grant_id><pubmed_authors>Liu X</pubmed_authors><pubmed_authors>Dai L</pubmed_authors><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Zhu K</pubmed_authors><pubmed_authors>Sun T</pubmed_authors><pubmed_authors>Fan S</pubmed_authors><pubmed_authors>Li N</pubmed_authors></additional><is_claimable>false</is_claimable><name>CD5L-associated gene analyses highlight the dysregulations, prognostic effects, immune associations, and drug-sensitivity predicative potentials of LCAT and CDC20 in hepatocellular carcinoma.</name><description>&lt;h4>Background&lt;/h4>The dysregulation of CD5L has been reported in hepatocellular carcinoma (HCC). However, its functions in HCC were controversial. In this study, we aimed to identify CD5L-associated pathways and markers and explore their values in HCC diagnosis, prognosis and treatment.&lt;h4>Methods&lt;/h4>HCC datasets with gene expression profiles and clinical data in TCGA and ICGC were downloaded. The immune/stroma cell infiltrations were estimated with xCell. CD5L-associated pathways and CD5L-associated genes (CD5L-AGs) were identified with gene expression comparisons and gene set enrichment analysis (GSEA). Cox regression, Kaplan-Meier survival analysis, and least absolute shrinkage and selection operator (LASSO) regression analysis were performed. The correlations of the key genes with im</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2026-05-29T18:48:09.195Z</modification><creation>2024-11-13T21:50:38.903Z</creation></dates><accession>S-EPMC9733014</accession><cross_references><pubmed>36494696</pubmed><doi>10.1186/s12935-022-02820-7</doi></cross_references></HashMap>