Chen Xiangling, Lin Jiatian, Chen Qiaoling, Liao Ximian, Wang Tongyu, Li Shi, Mao Longyi, Li Zesong
Guangdong Provincial Key Laboratory of Systems Biology and Synthetic Biology for Urogenital Tumors, Department of Urology, The First Affiliated Hospital of Shenzhen University, Shenzhen Second People's Hospital (Shenzhen Institute of Translational Medicine), Shenzhen, China.
Shenzhen Key Laboratory of Genitourinary Tumor, Department of Urology, The First Affiliated Hospital of Shenzhen University, Shenzhen Second People's Hospital (Shenzhen Institute of Translational Medicine), Shenzhen, China.
Front Genet. 2021 Sep 1;12:720979. doi: 10.3389/fgene.2021.720979. eCollection 2021.
Metastasis is the main cause of clear cell renal cell carcinoma (ccRCC) treatment failure, and the key genes involved in ccRCC metastasis remain largely unknown. We analyzed the ccRCC datasets in The Cancer Genome Atlas database, comparing primary and metastatic ccRCC tumor records in search of tumor metastasis-associated genes, and then carried out overall survival, Cox regression, and receiver operating characteristic (ROC) analyses to obtain potential prognostic markers. Comprehensive bioinformatics analysis was performed to verify that the checkpoint with forkhead associated and ring finger domains () gene is a reliable candidate oncogene, which is overexpressed in ccRCC metastatic tumor tissue, and that high expression levels of indicate a poor prognosis. A detailed analysis of the methylation of in ccRCC tumors showed that three sites within 200 bp of the transcription initiation site were significantly associated with prognosis and that hypomethylation was associated with increased gene expression levels. Knockdown of in ccRCC cells inhibited cell proliferation, colony formation, and migration ability. In summary, our findings suggest that the epigenetic signature on gene is a novel prognostic feature; furthermore, our findings offer theoretical support for the study of metastasis-related genes in ccRCC and provided new insights for the clinical treatment of the disease.
转移是透明细胞肾细胞癌(ccRCC)治疗失败的主要原因,而参与ccRCC转移的关键基因在很大程度上仍不清楚。我们分析了癌症基因组图谱数据库中的ccRCC数据集,比较原发性和转移性ccRCC肿瘤记录以寻找肿瘤转移相关基因,然后进行总生存、Cox回归和受试者工作特征(ROC)分析以获得潜在的预后标志物。进行了全面的生物信息学分析,以验证具有叉头相关和环指结构域()的检查点基因是一个可靠的候选癌基因,其在ccRCC转移瘤组织中过表达,并且的高表达水平表明预后不良。对ccRCC肿瘤中的甲基化进行详细分析表明,转录起始位点200 bp内的三个位点与预后显著相关,并且低甲基化与基因表达水平增加相关。在ccRCC细胞中敲低可抑制细胞增殖、集落形成和迁移能力。总之,我们的研究结果表明基因上的表观遗传特征是一种新的预后特征;此外,我们的研究结果为ccRCC转移相关基因的研究提供了理论支持,并为该疾病的临床治疗提供了新的见解。