Department of Urology, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China.
Shantou University Medical College, Shantou, China.
Front Immunol. 2022 May 23;13:830220. doi: 10.3389/fimmu.2022.830220. eCollection 2022.
Unlike early clear cell renal cell carcinoma (ccRCC), locally advanced and metastatic ccRCC present poor treatment outcomes and prognosis. As immune checkpoint inhibitors have achieved favorable results in the adjuvant treatment of metastatic ccRCC, we aimed to investigate the immunogenomic landscape during ccRCC progression and its potential impact on immunotherapy and prognosis. Using multi-omics and immunotherapy ccRCC datasets, an integrated analysis was performed to identify genomic alterations, immune microenvironment features, and related biological processes during ccRCC progression and evaluate their relevance to immunotherapy response and prognosis. We found that aggressive and metastatic ccRCC had higher proportions of genomic alterations, including mutations, Del(14q), Del(9p), and higher immunosuppressive cellular and molecular infiltration levels. Of these, the Del(14q) might mediate immune escape in ccRCC the VEGFA-VEGFR2 signaling pathway. Furthermore, immune-related pathways associated with ccRCC progression did not affect the immunotherapeutic response to ccRCC. Conversely, cell cycle pathways not only affected ccRCC progression and prognosis, but also were related to ccRCC immunotherapeutic response resistance. Overall, we described the immunogenomic characteristics of ccRCC progression and their correlations with immunotherapeutic response and prognosis, providing new insights into their prediction and the development of novel therapeutic strategies.
与早期透明细胞肾细胞癌 (ccRCC) 不同,局部晚期和转移性 ccRCC 的治疗效果和预后较差。由于免疫检查点抑制剂在转移性 ccRCC 的辅助治疗中取得了良好的效果,我们旨在研究 ccRCC 进展过程中的免疫基因组图谱及其对免疫治疗和预后的潜在影响。使用多组学和免疫治疗 ccRCC 数据集,进行了综合分析,以确定 ccRCC 进展过程中的基因组改变、免疫微环境特征和相关生物学过程,并评估它们与免疫治疗反应和预后的相关性。我们发现侵袭性和转移性 ccRCC 具有更高比例的基因组改变,包括 突变、Del(14q)、Del(9p),以及更高水平的免疫抑制性细胞和分子浸润。其中,Del(14q)可能通过 VEGFA-VEGFR2 信号通路介导 ccRCC 的免疫逃逸。此外,与 ccRCC 进展相关的免疫相关途径并不影响 ccRCC 的免疫治疗反应。相反,细胞周期途径不仅影响 ccRCC 的进展和预后,而且与 ccRCC 免疫治疗反应的耐药性有关。总的来说,我们描述了 ccRCC 进展的免疫基因组特征及其与免疫治疗反应和预后的相关性,为其预测和新治疗策略的开发提供了新的见解。