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Article: Single-cell transcriptome analysis reveals the association between histone lactylation and cisplatin resistance in bladder cancer

TitleSingle-cell transcriptome analysis reveals the association between histone lactylation and cisplatin resistance in bladder cancer
Authors
KeywordsBladder cancer
Cisplatin resistance
Histone lactylation
Transcription factors
Issue Date19-Jan-2024
PublisherElsevier
Citation
Drug Resistance Updates, 2024, v. 73 How to Cite?
Abstract

Patients with bladder cancer (BCa) frequently acquires resistance to platinum-based chemotherapy, particularly cisplatin. This study centered on the mechanism of cisplatin resistance in BCa and highlighted the pivotal role of lactylation in driving this phenomenon. Utilizing single-cell RNA sequencing, we delineated the single-cell landscape of Bca, pinpointing a distinctive subset of BCa cells that exhibit marked resistance to cisplatin with association with glycolysis metabolism. Notably, we observed that H3 lysine 18 lactylation (H3K18la) plays a crucial role in activating the transcription of target genes by enriching in their promoter regions. Targeted inhibition of H3K18la effectively restored cisplatin sensitivity in these cisplatin-resistant epithelial cells. Furthermore, H3K18la-driven key transcription factors YBX1 and YY1 promote cisplatin resistance in BCa. These findings enhance our understanding of the mechanisms underlying cisplatin resistance, offering valuable insights for identifying novel intervention targets to overcome drug resistance in Bca.


Persistent Identifierhttp://hdl.handle.net/10722/345979
ISSN
2023 Impact Factor: 15.8
2023 SCImago Journal Rankings: 4.665

 

DC FieldValueLanguage
dc.contributor.authorLi, Fei-
dc.contributor.authorZhang, Henghui-
dc.contributor.authorHuang, Yuan-
dc.contributor.authorLi, Dongqing-
dc.contributor.authorZheng, Zaosong-
dc.contributor.authorXie, Kunfeng-
dc.contributor.authorCao, Chun-
dc.contributor.authorWang, Qiong-
dc.contributor.authorZhao, Xinlei-
dc.contributor.authorHuang, Zehai-
dc.contributor.authorChen, Shijun-
dc.contributor.authorChen, Haiyong-
dc.contributor.authorFan, Qin-
dc.contributor.authorDeng, Fan-
dc.contributor.authorHou, Lina-
dc.contributor.authorDeng, Xiaolin-
dc.contributor.authorTan, Wanlong-
dc.date.accessioned2024-09-05T00:30:14Z-
dc.date.available2024-09-05T00:30:14Z-
dc.date.issued2024-01-19-
dc.identifier.citationDrug Resistance Updates, 2024, v. 73-
dc.identifier.issn1368-7646-
dc.identifier.urihttp://hdl.handle.net/10722/345979-
dc.description.abstract<p>Patients with bladder cancer (BCa) frequently acquires resistance to platinum-based chemotherapy, particularly cisplatin. This study centered on the mechanism of cisplatin resistance in BCa and highlighted the pivotal role of lactylation in driving this phenomenon. Utilizing single-cell RNA sequencing, we delineated the single-cell landscape of Bca, pinpointing a distinctive subset of BCa cells that exhibit marked resistance to cisplatin with association with glycolysis metabolism. Notably, we observed that H3 lysine 18 lactylation (H3K18la) plays a crucial role in activating the transcription of target genes by enriching in their promoter regions. Targeted inhibition of H3K18la effectively restored cisplatin sensitivity in these cisplatin-resistant epithelial cells. Furthermore, H3K18la-driven key transcription factors YBX1 and YY1 promote cisplatin resistance in BCa. These findings enhance our understanding of the mechanisms underlying cisplatin resistance, offering valuable insights for identifying novel intervention targets to overcome drug resistance in Bca.</p>-
dc.languageeng-
dc.publisherElsevier-
dc.relation.ispartofDrug Resistance Updates-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectBladder cancer-
dc.subjectCisplatin resistance-
dc.subjectHistone lactylation-
dc.subjectTranscription factors-
dc.titleSingle-cell transcriptome analysis reveals the association between histone lactylation and cisplatin resistance in bladder cancer-
dc.typeArticle-
dc.identifier.doi10.1016/j.drup.2024.101059-
dc.identifier.pmid38295753-
dc.identifier.scopuseid_2-s2.0-85183626089-
dc.identifier.volume73-
dc.identifier.eissn1532-2084-
dc.identifier.issnl1368-7646-

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