Zhang Zhechuan, Zhang Yuanfeng, Zhang Ronggui
Department of Urology, The Second Affiliated Hospital of Chongqing Medical University, 74 Linjiang Road, Yuzhong District, Chongqing, China.
The Second Clinical College, Chongqing Medical University, Chongqing, China.
Med Oncol. 2023 Jan 2;40(2):70. doi: 10.1007/s12032-022-01926-2.
Clear cell renal cell carcinoma (ccRCC) is the most common subtype of renal cell carcinoma. P4HA3 is a key enzyme in collagen biosynthesis and has emerged as important molecules in regulation of proliferation, invasion, and metastasis in various tumor types. The role of P4HA3 in the development of ccRCC has remained to be elucidated. Genes expression, prognostic, and enrichment analyses were carried out with bioinformatics analysis. The efficiency of P4HA3 knockdown was confirmed by real-time quantitative PCR and Western blotting. The cellular functions were analyzed by CCK-8, EdU, wound healing, and transwell assays. The levels of related proteins expression were analyzed by Western blotting. P4HA3 was highly expressed in ccRCC compared with normal tissue samples from the TCGA database. Kaplan-Meier curves results showed that the expression level of P4HA3 was significantly negatively correlated with overall survival of patients. P4HA3 expression knockdown inhibited the proliferation, migration, and invasion of ccRCC cells, as demonstrated by in vitro experiments. In addition, GSEA results revealed that P4HA3 may be related to EMT and involved in the PI3K-AKT-GSK3β pathway in ccRCC; this was tentatively confirmed through Western blotting. P4HA3 may induce ccRCC progression via the PI3K-AKT-GSK3β signaling pathway and could represent a potential therapeutic target.
透明细胞肾细胞癌(ccRCC)是肾细胞癌最常见的亚型。P4HA3是胶原蛋白生物合成中的关键酶,已成为多种肿瘤类型中调节增殖、侵袭和转移的重要分子。P4HA3在ccRCC发生发展中的作用尚待阐明。采用生物信息学分析进行基因表达、预后和富集分析。通过实时定量PCR和蛋白质免疫印迹法证实了P4HA3基因敲低的效率。通过CCK-8、EdU、伤口愈合和Transwell实验分析细胞功能。通过蛋白质免疫印迹法分析相关蛋白表达水平。与TCGA数据库中的正常组织样本相比,P4HA3在ccRCC中高表达。Kaplan-Meier曲线结果显示,P4HA3的表达水平与患者的总生存期显著负相关。体外实验表明,敲低P4HA3表达可抑制ccRCC细胞的增殖、迁移和侵袭。此外,基因集富集分析(GSEA)结果显示,P4HA3可能与上皮-间质转化(EMT)相关,并参与ccRCC的PI3K-AKT-GSK3β信号通路;蛋白质免疫印迹法初步证实了这一点。P4HA3可能通过PI3K-AKT-GSK3β信号通路诱导ccRCC进展,可能是一个潜在的治疗靶点。