<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>33(5)</volume><submitter>Wang Z</submitter><pubmed_abstract>A hypoxic tumor microenvironment (TME) promotes cancer progression, yet its value as a therapeutic target remains underexploited. Tripartite motif-containing 72 (TRIM72) may protect cells against various stresses including hypoxia. Recently, low TRIM72 expression has been implicated in cancer progression. However, the biological role and molecular mechanism of TRIM72 in breast cancer (BC) remain unclear. Herein, we analyzed the TRIM72 expression in BC tissue and cell lines by western blot (WB) and quantitative reverse transcription-PCR. We established the overexpression of TRIM72 using plasmids and lentiviral-mediated upregulation, as well as downregulation of protein phosphatase 3 catalytic subunit alpha (PPP3CA) by siRNA. The tumor-suppressive roles of TRIM72 were assessed on BT549 and M</pubmed_abstract><journal>Anti-cancer drugs</journal><pagination>489-501</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8997701</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>TRIM72 exerts antitumor effects in breast cancer and modulates lactate production and MCT4 promoter activity by interacting with PPP3CA.</pubmed_title><pmcid>PMC8997701</pmcid><pubmed_authors>Qiu Y</pubmed_authors><pubmed_authors>Li H</pubmed_authors><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Li K</pubmed_authors><pubmed_authors>Wang Z</pubmed_authors><pubmed_authors>Zhang Q</pubmed_authors></additional><is_claimable>false</is_claimable><name>TRIM72 exerts antitumor effects in breast cancer and modulates lactate production and MCT4 promoter activity by interacting with PPP3CA.</name><description>A hypoxic tumor microenvironment (TME) promotes cancer progression, yet its value as a therapeutic target remains underexploited. Tripartite motif-containing 72 (TRIM72) may protect cells against various stresses including hypoxia. Recently, low TRIM72 expression has been implicated in cancer progression. However, the biological role and molecular mechanism of TRIM72 in breast cancer (BC) remain unclear. Herein, we analyzed the TRIM72 expression in BC tissue and cell lines by western blot (WB) and quantitative reverse transcription-PCR. We established the overexpression of TRIM72 using plasmids and lentiviral-mediated upregulation, as well as downregulation of protein phosphatase 3 catalytic subunit alpha (PPP3CA) by siRNA. The tumor-suppressive roles of TRIM72 were assessed on BT549 and M</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jun</publication><modification>2026-06-18T05:03:36.195Z</modification><creation>2025-05-31T23:34:20.417Z</creation></dates><accession>S-EPMC8997701</accession><cross_references><pubmed>35324524</pubmed><doi>10.1097/CAD.0000000000001304</doi></cross_references></HashMap>