Dissecting LncRNA Roles in Renal Cell Carcinoma Metastasis and Characterizing Genomic Heterogeneity by Single-Cell RNA-seq

被引:24
作者
Li, Xue [1 ,2 ,3 ]
Meng, Xianwen [1 ]
Wei, Cong [3 ]
Zhou, Yincong [1 ]
Chen, Hongjun [1 ]
Huang, He [3 ]
Chen, Ming [1 ,2 ]
机构
[1] Zhejiang Univ, Coll Life Sci, Dept Bioinformat, Hangzhou, Zhejiang, Peoples R China
[2] Zhejiang Univ, James D Watson Inst Genome Sci, Hangzhou, Zhejiang, Peoples R China
[3] Zhejiang Univ, Sch Med, Affiliated Hosp 1, Bone Marrow Transplantat Ctr, Hangzhou, Zhejiang, Peoples R China
关键词
LONG NONCODING RNA; EPITHELIAL-MESENCHYMAL TRANSITION; INTRA-TUMOR HETEROGENEITY; CANCER; EXPRESSION; INFLAMMATION; EVOLUTION; PROSTATE; PROMOTES; THERAPY;
D O I
10.1158/1541-7786.MCR-17-0776
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Long noncoding RNAs (lncRNA) have recently emerged as important regulators in cancer cell proliferation and metastasis. However, the role of lncRNAs in metastatic clear cell renal cell carcinoma (ccRCC) remains unclear. Here, single-cell RNA sequencing data were analyzed from primary renal cell carcinoma and paired metastatic renal cell carcinoma specimens, and characterized the expression profiles of over 10,000 genes, including 1,874 lncRNAs. Further analysis revealed that lncRNAs exhibit cancer type-and tissue-specific expression across ccRCC cells. Interestingly, a number of lncRNAs (n = 173) associated with ccRCC metastasis, termed ccRCC metastasis-associated lncRNAs (CMAL). Moreover, functional analysis based on a CMAL-PCG coexpression network revealed that CMALs contribute to cell adhesion, immune response, and cell proliferation. Incombination with survival analysis, 12 CMALs were identified that participate in TNF and hypoxia-inducible factor 1 signaling to promote ccRCC metastasis. Further investigation on intratumoral heterogeneity showed that some CMALs are selectively expressed in different subpopulations. Implications: To explore ccRCC metastasis, the current study performed a global dissection of lncRNAs and a complex genomic analysis of ccRCC tumor heterogeneity. The data shed light on the discovery of potential lncRNA biomarkers and lncRNA therapeutic targets. (C) 2018 AACR.
引用
收藏
页码:1879 / 1888
页数:10
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