m6A modification patterns and tumor immune landscape in clear cell renal carcinoma

被引:54
作者
Zhong, Jiehui [1 ,2 ]
Liu, Zezhen [1 ,2 ]
Cai, Chao [1 ,2 ]
Duan, Xiaolu [1 ,2 ]
Deng, Tuo [1 ,2 ]
Zeng, Guohua [1 ,2 ]
机构
[1] Guangzhou Med Univ, Dept Urol, Minimally Invas Surg Ctr, Affiliated Hosp 1, Guangzhou, Guangdong, Peoples R China
[2] Guangdong Key Lab Urol, Guangzhou, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
immunotherapy; kidney neoplasms; CTLA-4; BLOCKADE; EXPRESSION; SENSITIVITY; SUBSETS; CANCER;
D O I
10.1136/jitc-2020-001646
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Recent studies have focused on the correlation between N6-methyladenosine (m(6)A) modification and specific tumor-infiltrating immune cells. However, the potential roles of m(6)A modification in the tumor immune landscape remain elusive. Methods We comprehensively evaluated the m(6)A modification patterns and tumor immune landscape of 513 clear cell renal cell carcinoma (ccRCC) patients, and correlated the m(6)A modification patterns with the immune landscape. The m6Ascore was established using principal component analysis. Multivariate Cox regression analysis was performed to evaluate the prognostic value of the m6Ascore. Results We identified three m6Aclusters-characterized by differences in Th17 signature, extent of intratumor heterogeneity, overall cell proliferation, aneuploidy, expression of immunomodulatory genes, overall somatic copy number alterations, and prognosis. The m6Ascore was established to quantify the m(6)A modification pattern of individual ccRCC patients. Further analyses revealed that the m6Ascore was an independent prognostic factor of ccRCC. Finally, we verified the prognostic value of the m6Ascore in the programmed cell death protein 1 (PD-1) blockade therapy of patients with advanced ccRCC. Conclusions This study demonstrated the correlation between m(6)A modification and the tumor immune landscape in ccRCC. The comprehensive evaluation of m(6)A modification patterns in individual ccRCC patients enhances our understanding of the tumor immune landscape and provides a new approach toward new and improved immunotherapeutic strategies for ccRCC patients.
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页数:12
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