<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Li X</submitter><funding>Scientific and Technological Research Project of Xinjiang Production and Construction Corps</funding><funding>Xinjiang Production and Construction Corps Key Areas Innovation Team Project</funding><funding>Projects of Shihezi University</funding><funding>Natural Science Foundation of Jilin Province</funding><pagination>426</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10173472</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>23(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>In previous study, we found that the content of medium-chain fatty acid Caprylic Acid (FFA C8:0) may be an important risk factor of obesity induced prostate cancer (PCa). However, the relationship between FFA C8:0 and PCa has not been reported. In this study, we explored whether the FFA C8:0 can promotes the progression of PCa by up-regulating Krüppel-like factor 7 (KLF7).&lt;h4>Methods&lt;/h4>We collected tissues from PCa patients and Benign Prostate Hyperplasia (BPH), constructed a primary-tumor bearing mouse model with obesity through high-fat diet, and observed the tumor formation ability of PCa cells. In vitro, CCK8 assay, plate cloning, Transwell and scratch experiment were used to detect the changes in biological behavior of PCa cells stimulated by FFA C8:0.&lt;h4>Results&lt;</pubmed_abstract><journal>BMC cancer</journal><pubmed_title>Caprylic Acid (FFA C8:0) promotes the progression of prostate cancer by up-regulating G protein-coupled receptor 84/ Kruppel-like factor 7.</pubmed_title><pmcid>PMC10173472</pmcid><funding_grant_id>2021AB028</funding_grant_id><funding_grant_id>GJHZ201703</funding_grant_id><funding_grant_id>2018AB018</funding_grant_id><funding_grant_id>202210759016</funding_grant_id><funding_grant_id>81760518</funding_grant_id><funding_grant_id>2018CB002</funding_grant_id><funding_grant_id>ZZZC202017A</funding_grant_id><funding_grant_id>ZZZC201817A</funding_grant_id><pubmed_authors>Li W</pubmed_authors><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Yuan C</pubmed_authors><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>Xie J</pubmed_authors><pubmed_authors>Yang B</pubmed_authors><pubmed_authors>Pang H</pubmed_authors><pubmed_authors>Ma D</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Li M</pubmed_authors><pubmed_authors>Tang Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Caprylic Acid (FFA C8:0) promotes the progression of prostate cancer by up-regulating G protein-coupled receptor 84/ Kruppel-like factor 7.</name><description>&lt;h4>Background&lt;/h4>In previous study, we found that the content of medium-chain fatty acid Caprylic Acid (FFA C8:0) may be an important risk factor of obesity induced prostate cancer (PCa). However, the relationship between FFA C8:0 and PCa has not been reported. In this study, we explored whether the FFA C8:0 can promotes the progression of PCa by up-regulating Krüppel-like factor 7 (KLF7).&lt;h4>Methods&lt;/h4>We collected tissues from PCa patients and Benign Prostate Hyperplasia (BPH), constructed a primary-tumor bearing mouse model with obesity through high-fat diet, and observed the tumor formation ability of PCa cells. In vitro, CCK8 assay, plate cloning, Transwell and scratch experiment were used to detect the changes in biological behavior of PCa cells stimulated by FFA C8:0.&lt;h4>Results&lt;</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 May</publication><modification>2025-04-26T22:39:01.303Z</modification><creation>2025-04-06T17:16:13.88Z</creation></dates><accession>S-EPMC10173472</accession><cross_references><pubmed>37170248</pubmed><doi>10.1186/s12885-023-10841-2</doi></cross_references></HashMap>