Chen Yinwei, Liu Zhanpeng, Yu Qian, Sun Xu, Wang Shuai, Zhu Qingyi, Yang Jian, Jiang Rongjiang
Department of Urology, The Second Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Department of Urology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Int J Genomics. 2023 May 23;2023:5542233. doi: 10.1155/2023/5542233. eCollection 2023.
Post-renal transplant patients have a high likelihood of developing renal cancer. However, the underlying biological mechanisms behind the development of renal cancer in post-kidney transplant patients remain to be elucidated. Therefore, this study aimed to investigate the underlying biological mechanism behind the development of renal cell carcinoma in post-renal transplant patients.
Next-generation sequencing data and corresponding clinical information of patients with clear cell renal cell carcinoma (ccRCC) were obtained from The Cancer Genome Atlas Program (TCGA) database. The microarray data of kidney transplant patients with or without rejection response was obtained from the Gene Expression Omnibus (GEO) database. In addition, statistical analysis was conducted in R software.
We identified 55 upregulated genes in the transplant patients with rejection from the GEO datasets (GSE48581, GSE36059, and GSE98320). Furthermore, we conducted bioinformatics analyses, which showed that all of these genes were upregulated in ccRCC tissue. Moreover, a prognosis model was constructed based on four rejection-related genes, including , , , and . The prognosis model showed excellent performance in prognosis prediction in a ccRCC cohort. In addition, the machine learning algorithms identified 19 rejection-related genes, including , involved in ccRCC occurrence. Finally, the was selected for further research, including its clinical and biological role.
In all, our study provides novel insight into the transition from the rejection of renal transplant to renal cancer. Meanwhile, could be a potential biomarker for ccRCC diagnosis and prognosis in post-kidney transplant patients.
肾移植术后患者发生肾癌的可能性很高。然而,肾移植术后患者发生肾癌的潜在生物学机制仍有待阐明。因此,本研究旨在探讨肾移植术后患者发生肾细胞癌的潜在生物学机制。
从癌症基因组图谱计划(TCGA)数据库中获取透明细胞肾细胞癌(ccRCC)患者的二代测序数据及相应临床信息。从基因表达综合数据库(GEO)中获取有或无排斥反应的肾移植患者的微阵列数据。此外,在R软件中进行统计分析。
我们从GEO数据集(GSE48581、GSE36059和GSE98320)中鉴定出55个在有排斥反应的移植患者中上调的基因。此外,我们进行了生物信息学分析,结果显示所有这些基因在ccRCC组织中均上调。此外,基于四个与排斥反应相关的基因构建了一个预后模型,包括 、 、 和 。该预后模型在ccRCC队列的预后预测中表现出色。此外,机器学习算法鉴定出19个与排斥反应相关的基因,包括 ,参与ccRCC的发生。最后,选择 进行进一步研究,包括其临床和生物学作用。
总之,我们的研究为从肾移植排斥反应向肾癌的转变提供了新的见解。同时, 可能是肾移植术后患者ccRCC诊断和预后的潜在生物标志物。