Zhang Xuezhou, Hong Baoan, Yu Wei, Miao Qi, Wang Wei, Wang Yuxuan, Sun Zhipeng, Bo Yuxuan, Zhang Jiqing, Zhang Huina, Zhang Ning
Department of Urology, Beijing Anzhen Hospital, Capital Medical University, Beijing 100029, China.
Department of Urology, Beijing Anzhen Hospital, Capital Medical University, Beijing 100029, China.
Int J Biol Macromol. 2025 May;307(Pt 3):142079. doi: 10.1016/j.ijbiomac.2025.142079. Epub 2025 Mar 18.
CD70, a member of the tumor necrosis factor family, has been implicated in various cellular processes associated with tumorigenesis. Despite its known expression in certain cancers, a detailed pan-cancer analysis and functional validation in clear cell renal cell carcinoma (ccRCC) have not been comprehensively explored. We conducted a pan-cancer analysis using publicly available databases to investigate the expression and prognostic significance of CD70 across various cancer types. For functional validation, immunohistochemistry was performed on ccRCC and adjacent normal tissues to evaluate CD70 expression levels. Additionally, ccRCC organoid model was developed and subjected to CAR-T cell cytotoxicity assays to evaluate the efficacy of targeting CD70 in vitro. The pan-cancer analysis revealed elevated expression of CD70 in several cancer types, including ccRCC, where it correlated with poor prognosis. Immunohistochemical analysis confirmed significant overexpression of CD70 in ccRCC tissues compared to normal tissues. In the ccRCC organoid model, CAR-T cells targeting CD70 demonstrated effective cytotoxicity against organoids expressing CD70. The overexpression of CD70 across diverse cancer types underscores its potential as a universal biomarker. Importantly, our findings underscore the clinical relevance of CD70 as a critical oncogenic factor and a promising therapeutic target in ccRCC, with implications for advancing personalized medicine.
CD70是肿瘤坏死因子家族的一员,与肿瘤发生相关的多种细胞过程有关。尽管已知其在某些癌症中表达,但在透明细胞肾细胞癌(ccRCC)中尚未对其进行全面的泛癌分析和功能验证。我们使用公开可用的数据库进行了泛癌分析,以研究CD70在各种癌症类型中的表达及预后意义。为进行功能验证,对ccRCC及相邻正常组织进行免疫组织化学分析,以评估CD70的表达水平。此外,构建了ccRCC类器官模型,并进行CAR-T细胞细胞毒性试验,以评估体外靶向CD70的疗效。泛癌分析显示,包括ccRCC在内的几种癌症类型中CD70表达升高,且与预后不良相关。免疫组织化学分析证实,与正常组织相比,ccRCC组织中CD70明显过表达。在ccRCC类器官模型中,靶向CD70的CAR-T细胞对表达CD70的类器官表现出有效的细胞毒性。CD70在多种癌症类型中的过表达突出了其作为通用生物标志物的潜力。重要的是,我们的研究结果强调了CD70作为ccRCC中关键致癌因子和有前景的治疗靶点的临床相关性,对推进个性化医疗具有重要意义。