A Novel Long Noncoding RNA Finetunes the DNA Damage Response in Hepatocellular Carcinoma

被引:2
作者
Barcena-Varela, Marina [1 ,2 ,3 ,4 ,5 ,6 ]
Lujambio, Amaia [1 ,2 ,3 ,4 ,5 ]
机构
[1] Icahn Sch Med Mt Sinai, Dept Oncol Sci, 1 Gustave L Levy Pl, New York, NY 10029 USA
[2] Icahn Sch Med Mt Sinai, Dept Med, Liver Canc Program, New York, NY 10029 USA
[3] Icahn Sch Med Mt Sinai, Dept Med, Div Liver Dis, New York, NY 10029 USA
[4] Icahn Sch Med Mt Sinai, Tisch Canc Inst, New York, NY 10029 USA
[5] Icahn Sch Med Mt Sinai, Precis Immunol Inst, New York, NY 10029 USA
[6] Icahn Sch Med Mt Sinai, Grad Sch Biomed Sci, New York, NY 10029 USA
基金
欧盟地平线“2020”;
关键词
D O I
10.1158/0008-5472.CAN-21-2776
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The study by Unfried and colleagues reports the intriguing discovery of a novel long noncoding RNA (lncRNA) with a critical role in the regulation of DNA damage response in hepatocellular carcinoma. Providing an exhaustive and detailed characterization of the complex network interactions within the double-stranded breaks in the DNA, the authors demonstrated that NIHCOLE serves as a scaffold and facilitator of nonhomologous end-joining machinery. This study greatly contributes to the growing evidence supporting the key roles of ncRNAs in health and disease. Although larger studies are needed to understand the potential of lncRNAs to improve the clinical management of patients with cancer, this study demonstrates that high expression of NIHCOLE may be associated with an impaired response to DNA damage-based therapies, in part through its role in preventing cell death.
引用
收藏
页码:4899 / 4900
页数:2
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