<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13(9)</volume><submitter>Fu Y</submitter><pubmed_abstract>&lt;b>Rationale:&lt;/b> Cisplatin, a potent chemotherapeutic drug, induces side effects in normal tissues including the kidney. To reduce the side effects, repeated low-dose cisplatin (RLDC) is commonly used in clinical setting. While RLDC reduces acute nephrotoxicity to certain extents, a significant portion of patients later develop chronic kidney problems, underscoring the need for novel therapeutics to alleviate the long-term sequelae of RLDC therapy. &lt;b>Methods:&lt;/b> &lt;i>In vivo&lt;/i>, the role of HMGB1 was examined by testing HMGB1 neutralizing antibodies in RLDC mice. &lt;i>In vitro&lt;/i>, the effects of HMGB1 knockdown on RLDC-induced nuclear factor-κB (NF-κB) activation and fibrotic phenotype changes were tested in proximal tubular cells. To study signal transducer and activator of transcription</pubmed_abstract><journal>Theranostics</journal><pagination>2757-2773</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10240827</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The STAT1/HMGB1/NF-κB pathway in chronic inflammation and kidney injury after cisplatin exposure.</pubmed_title><pmcid>PMC10240827</pmcid><pubmed_authors>Liu Z</pubmed_authors><pubmed_authors>Dong Z</pubmed_authors><pubmed_authors>Tang C</pubmed_authors><pubmed_authors>Cai J</pubmed_authors><pubmed_authors>Chen G</pubmed_authors><pubmed_authors>Fu Y</pubmed_authors><pubmed_authors>Xiang Y</pubmed_authors><pubmed_authors>Zha J</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Yang D</pubmed_authors></additional><is_claimable>false</is_claimable><name>The STAT1/HMGB1/NF-κB pathway in chronic inflammation and kidney injury after cisplatin exposure.</name><description>&lt;b>Rationale:&lt;/b> Cisplatin, a potent chemotherapeutic drug, induces side effects in normal tissues including the kidney. To reduce the side effects, repeated low-dose cisplatin (RLDC) is commonly used in clinical setting. While RLDC reduces acute nephrotoxicity to certain extents, a significant portion of patients later develop chronic kidney problems, underscoring the need for novel therapeutics to alleviate the long-term sequelae of RLDC therapy. &lt;b>Methods:&lt;/b> &lt;i>In vivo&lt;/i>, the role of HMGB1 was examined by testing HMGB1 neutralizing antibodies in RLDC mice. &lt;i>In vitro&lt;/i>, the effects of HMGB1 knockdown on RLDC-induced nuclear factor-κB (NF-κB) activation and fibrotic phenotype changes were tested in proximal tubular cells. To study signal transducer and activator of transcription</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023</publication><modification>2026-05-29T03:28:01.781Z</modification><creation>2025-04-06T11:13:49.751Z</creation></dates><accession>S-EPMC10240827</accession><cross_references><pubmed>37284446</pubmed><doi>10.7150/thno.81406</doi></cross_references></HashMap>