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

被引:44
|
作者
Li, Fei [1 ]
Zhang, Henghui [1 ]
Huang, Yuan [1 ]
Li, Dongqing [1 ]
Zheng, Zaosong [1 ]
Xie, Kunfeng [1 ]
Cao, Chun [1 ]
Wang, Qiong [1 ]
Zhao, Xinlei [1 ]
Huang, Zehai [1 ]
Chen, Shijun [1 ]
Chen, Haiyong [2 ]
Fan, Qin [3 ]
Deng, Fan [4 ]
Hou, Lina [5 ]
Deng, Xiaolin [6 ]
Tan, Wanlong [1 ]
机构
[1] Southern Med Univ, Nanfang Hosp, Dept Urol, Guangzhou, Guangdong, Peoples R China
[2] Univ Hong Kong, LKS Fac Med, Sch Chinese Med, Pokfulam, R619,3 Sassoon Rd, Hong Kong, Peoples R China
[3] Southern Med Univ, Sch Tradit Chinese Med, Guangzhou, Peoples R China
[4] Southern Med Univ, Sch Basic Med Sci, Dept Cell Biol, Guangzhou, Peoples R China
[5] Southern Med Univ, Nanfang Hosp, Dept Hlth Management, Guangzhou, Peoples R China
[6] Ganzhou Peoples Hosp, Dept Urol, Ganzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
Bladder cancer; Cisplatin resistance; Histone lactylation; Transcription factors; BINDING-PROTEIN YB-1; R PACKAGE; METASTASIS; SENSITIVITY; METABOLISM; EXPRESSION; CARCINOMA;
D O I
10.1016/j.drup.2024.101059
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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.
引用
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页数:15
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