Zhang Si-Han, Zeng Na, Sun Jian-Xuan, Liu Chen-Qian, Xu Jin-Zhou, Xu Meng-Yao, An Ye, Zhong Xing-Yu, Ma Si-Yang, He Hao-Dong, Xia Qi-Dong, Hu Jia, Wang Shao-Gang
Department and Institute of Urology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, No. 1095 Jiefang Avenue, 430030, Wuhan, China.
Heliyon. 2023 May 29;9(6):e16644. doi: 10.1016/j.heliyon.2023.e16644. eCollection 2023 Jun.
Cereblon (CRBN) has emerged as a vital E3 ubiquitin ligase for Proteolysis-targeting chimera (PROTAC) design. However, few studies focus on the physiological mechanism of CRBN, and more studies are needed to explore the influence of CRBN on tumorigenesis. This pan-cancer analysis aims to explore the prognostic and immunologic roles of CRBN, and provide new insight for CRBN into cancer treatment and PROTAC design.
The TCGA database, TIMER 2.0 database, and TISIDB database were used to analyze the role of CRBN in pan-cancer. Multiple bioinformatic methods (ssGSEA, Kaplan-Meier, univariate cox regression, ESTIMATE, CIBERSORT) were applied to investigate the CRBN expression status, gene activity, prognostic values, and its correlation with immune scores, immune infiltration, immune-related functions, HALLMARKs functions, and response to immunotherapy in pan-cancer.
In most cancer types, the expression and activity of CRBN in tumor groups were lower compared with normal groups. Upregulated CRBN expression may indicate a better prognosis for cancer patients. The Immune score, stromal score, and tumor purity varied greatly among different cancer types. GSEA analysis showed that high CRBN expression was correlated with the downregulation of tumor-promoting signaling pathways. The level of CRBN was associated with Tumor mutation burden (TMB), Microsatellite instability (MSI), objective response rate (ORR), and immune cell infiltration in a few cancer types.
Pan-cancer analysis reveals the potential role of CRBN as a prognostic biomarker and versatile immunologic roles in different cancer types. Upregulated expression of CRBN may be beneficial to CRBN-related immunotherapy and PROTAC design.
cereblon(CRBN)已成为用于靶向蛋白水解嵌合体(PROTAC)设计的重要E3泛素连接酶。然而,很少有研究关注CRBN的生理机制,需要更多研究来探索CRBN对肿瘤发生的影响。这项泛癌分析旨在探讨CRBN的预后和免疫作用,并为CRBN在癌症治疗和PROTAC设计方面提供新的见解。
使用TCGA数据库、TIMER 2.0数据库和TISIDB数据库分析CRBN在泛癌中的作用。应用多种生物信息学方法(单样本基因集富集分析、Kaplan-Meier法、单变量cox回归、ESTIMATE、CIBERSORT)研究CRBN的表达状态、基因活性、预后价值及其与泛癌中免疫评分、免疫浸润、免疫相关功能、HALLMARKs功能和免疫治疗反应的相关性。
在大多数癌症类型中,肿瘤组中CRBN的表达和活性低于正常组。CRBN表达上调可能表明癌症患者预后较好。不同癌症类型之间的免疫评分、基质评分和肿瘤纯度差异很大。基因集富集分析表明,CRBN高表达与肿瘤促进信号通路的下调相关。在少数癌症类型中,CRBN水平与肿瘤突变负荷(TMB)、微卫星不稳定性(MSI)、客观缓解率(ORR)和免疫细胞浸润有关。
泛癌分析揭示了CRBN作为预后生物标志物的潜在作用以及在不同癌症类型中的多种免疫作用。CRBN表达上调可能有利于与CRBN相关的免疫治疗和PROTAC设计。