Integrative analysis of senescence-related genes identifies robust prognostic clusters with distinct features in hepatocellular carcinoma

被引:2
|
作者
Liu, Sicheng [1 ,2 ,3 ]
Meng, Yang [1 ,2 ,3 ]
Zhang, Yaguang [1 ,2 ,3 ]
Qiu, Lei [1 ,2 ,3 ]
Wan, Xiaowen [1 ,2 ,3 ]
Yang, Xuyang [4 ]
Zhang, Yang [4 ]
Liu, Xueqin [1 ,2 ,3 ]
Wen, Linda [1 ,2 ,3 ]
Lei, Xue [1 ,2 ,3 ]
Zhang, Bo [4 ]
Han, Junhong [1 ,2 ,3 ]
机构
[1] Sichuan Univ, West China Hosp, Canc Ctr, Dept Biotherapy, Chengdu 610041, Peoples R China
[2] Sichuan Univ, West China Hosp, State Key Lab Biotherapy, Chengdu 610041, Peoples R China
[3] Sichuan Univ, West China Hosp, Frontiers Sci Ctr Dis Related Mol Network, Chengdu 610041, Peoples R China
[4] Sichuan Univ, West China Hosp, Frontiers Sci Ctr Dis Related Mol Network, Dept Gen Surg,Res Lab Canc Epigenet & Genom, Chengdu 610041, Peoples R China
关键词
Senescence-related genes; Hepatocellular carcinoma; Prognostic clusters; Senescence-associated stemness; Therapeutic strategy; Computational method; CANCER; INHIBITOR; DISCOVERY; RESOURCE; THERAPY; PACKAGE; PATHWAY;
D O I
10.1016/j.jare.2024.04.007
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Introduction: Senescence refers to a state of permanent cell growth arrest and is regarded as a tumor suppressive mechanism, whereas accumulative evidence demonstrate that senescent cells play an adverse role during cancer progression. The scarcity of specific and reliable markers reflecting senescence level in cancer impede our understanding of this biological basis. Objectives: Senescence-related genes (SRGs) were collected for integrative analysis to reveal the role of senescence in hepatocellular carcinoma (HCC). Methods: Consensus clustering was used to subtype HCC based on SRGs. Several computational methods, including single sample gene set enrichment analysis (ssGSEA), fuzzy c-means algorithm, were performed. Data of drug sensitivities were utilized to screen potential therapeutic agents for different senescence patients. Additionally, we developed a method called signature-related gene analysis (SRGA) for identification of markers relevant to phenotype of interest. Experimental strategies consisting quantitative real-time PCR (qRT-PCR), b-galactosidase assay, western blot, and tumor-T cell co-culture system were used to validate the findings in vitro. Results: We identified three robust prognostic clusters of HCC patients with distinct survival outcome, mutational landscape, and immune features. We further extracted signature genes of senescence clusters to construct the senescence scoring system and profile senescence level in HCC at bulk and single-cell resolution. Senescence-induced stemness reprogramming was confirmed both in silico and in vitro. HCC patients with high senescence were immune suppressed and sensitive to Tozasertib and other drugs. We suggested that MAFG, PLIN3, and 4 other genes were pertinent to HCC senescence, and MAFG potentially mediated immune suppression, senescence, and stemness. Conclusion: Our findings provide insights into the role of SRGs in patients stratification and precision medicine. (c) 2024 The Authors. Published by Elsevier B.V. on behalf of Cairo University. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:107 / 123
页数:17
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