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组蛋白乳酸化相关基因与癌症相关成纤维细胞的分子模式和功能相关,在透明细胞肾细胞癌中具有重要的临床意义。

Histone lactylation-related genes correlate with the molecular patterns and functions of cancer-associated fibroblasts and have significant clinical implications in clear cell renal cell carcinoma.

作者信息

Kong Weiyu, He Jiaxin, Zhou Qinyao, Zhou Xin, Wei Xiyi, Yang Yonglin, Mei Yiwen, Wang Shuai, Zhang Xi, Yao Bing, Yue Yulin, Xu Jiali, Jiang Minjun, Xu Chen

机构信息

Department of Urology, Suzhou Ninth People's Hospital, Soochow University, Suzhou, 215000, China.

Department of Urology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, 210029, China.

出版信息

Heliyon. 2024 Jun 24;10(13):e33554. doi: 10.1016/j.heliyon.2024.e33554. eCollection 2024 Jul 15.

DOI:10.1016/j.heliyon.2024.e33554
PMID:39035489
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11259888/
Abstract

Recent research emphasised the indispensable role of histone lactylation in the activation of hepatic stellate cells. The VHL mutation is extremely common in clear cell renal cell carcinoma, which normally causes a metabolic shift in cancer cells and increases lactate production, eventually creating a lactate-enriched tumour microenvironment. Cancer-associated fibroblasts (CAFs) promote tumour progression, which is also vital in clear cell renal cell carcinoma. Therefore, this study investigated histone lactylation in CAFs and its impact on patient survival. Multiomics technology was employed to determine the role of histone lactylation-related genes in the evolution of CAFs which correlated with the function and molecular signatures of CAFs. The results suggested that TIMP1 was the hub gene of histone lactylation-related genes in clear cell renal cell carcinoma.

摘要

近期研究强调了组蛋白乳酸化在肝星状细胞激活中的不可或缺作用。VHL突变在透明细胞肾细胞癌中极为常见,这通常会导致癌细胞发生代谢转变并增加乳酸生成,最终形成富含乳酸的肿瘤微环境。癌症相关成纤维细胞(CAFs)促进肿瘤进展,这在透明细胞肾细胞癌中也至关重要。因此,本研究调查了CAFs中的组蛋白乳酸化及其对患者生存的影响。采用多组学技术来确定组蛋白乳酸化相关基因在CAFs演变中的作用,这些基因与CAFs的功能和分子特征相关。结果表明,TIMP1是透明细胞肾细胞癌中组蛋白乳酸化相关基因的枢纽基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0f6/11259888/dfaa1a27a93e/gr9.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0f6/11259888/dfaa1a27a93e/gr9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0f6/11259888/86a5c2be83b5/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0f6/11259888/035ae3e2772a/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0f6/11259888/03ff893029da/gr3.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0f6/11259888/dd91186e90fd/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0f6/11259888/60541eebe096/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0f6/11259888/dfaa1a27a93e/gr9.jpg

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2
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