Identification of Potential Long Non-coding RNA Expression Quantitative Trait Methylations in Lung Adenocarcinoma and Lung Squamous Carcinoma.
Identification of Potential Long Non-coding RNA Expression Quantitative Trait Methylations in Lung Adenocarcinoma and Lung Squamous Carcinoma.
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肺腺癌和肺鳞癌中潜在的长非编码 RNA 表达定量特征甲基化的鉴定
DOI:
10.3389/fgene.2020.602035
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发表时间:
2020
影响因子:
3.7
通讯作者:
Wang G
中科院分区:
文献类型:
--
作者:
Wu X;Gao Y;Bu J;Deng L;Zhang P;Chi M;Jiang L;Shi X;Ning S;Wang G
There are associations between DNA methylation and the expression of long non-coding RNA (lncRNA), also known as lncRNA expression quantitative trait methylations (lnc-eQTMs). Lnc-eQTMs may induce a wide range of carcinogenesis pathways. However, lnc-eQTMs have not been globally identified and studied, and their roles in lung adenocarcinoma (LUAD) and lung squamous carcinoma (LUSC) are largely unknown. In the present study, we identified some differential methylation sites located in genes of long intergenic non-coding RNAs (lincRNAs) and other types of lncRNAs in LUAD and LUSC. An integrated pipeline was established to construct two global cancer-specific regulatory networks of lnc-eQTMs in LUAD and LUSC. The associations between eQTMs showed common and specific features between LUAD and LUSC. Some lnc-eQTMs were also related with survival in LUAD- and LUSC-specific regulatory networks. Lnc-eQTMs were associated with cancer-related functions, such as lung epithelium development and vasculogenesis by functional analysis. Drug repurposing analysis revealed that these lnc-eQTMs may mediate the effects of some anesthesia-related drugs in LUAD and LUSC. In summary, the present study elucidates the roles of lnc-eQTMs in LUAD and LUSC, which could improve our understanding of lung cancer pathogenesis and facilitate treatment.
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影响因子:
14.9
作者:
Kuleshov MV;Jones MR;Rouillard AD;Fernandez NF;Duan Q;Wang Z;Koplev S;Jenkins SL;Jagodnik KM;Lachmann A;McDermott MG;Monteiro CD;Gundersen GW;Ma'ayan A
通讯作者:
Ma'ayan A
影响因子:
14.9
作者:
Zhi H;Li X;Wang P;Gao Y;Gao B;Zhou D;Zhang Y;Guo M;Yue M;Shen W;Ning S;Jin L;Li X
通讯作者:
Li X
影响因子:
2.8
作者:
Kaessmeyer, Sabine;Bhoola, Kanti;Plendl, Johanna
通讯作者:
Plendl, Johanna
DOI:
10.1126/science.1192002
发表时间:
2010-08-06
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
Tsai MC;Manor O;Wan Y;Mosammaparast N;Wang JK;Lan F;Shi Y;Segal E;Chang HY
通讯作者:
Chang HY
影响因子:
2
作者:
Chu, Chin-Nan;Wu, King-Chuen;Chung, Jing-Gung
通讯作者:
Chung, Jing-Gung