4.7 Review

Long noncoding RNA: A resident staff of genomic instability regulation in tumorigenesis

Journal

CANCER LETTERS
Volume 503, Issue -, Pages 103-109

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.canlet.2021.01.021

Keywords

LncRNAs; Chromosomal instability; Chromatin higher structures; DNA double-Strand break; Tumor initiation

Categories

Funding

  1. Research on Chronic Noncommunicable Diseases Prevention and Control of National Ministry of Science and Technology [2016YFC1303804]
  2. National Natural Science Foundation of China [81672275, 81874052, 3A214DJ63428, 82050003]
  3. Youth Fund of the National Natural Science Foundation of China [81802487]
  4. Youth Development Foundation of the First Hospital of Jilin university [JDYY92018028, 2020-ZL-06]

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Genomic instability is a key feature of cancer, potentially promoting tumorigenesis by increasing gene destruction and loss of genome integrity. Studies have shown that long noncoding RNAs play a significant role in regulating genomic stability.
Genomic instability is an important characteristic of cancer, which promotes clonal evolution and tumorigenesis by increasing the frequency of gene destruction and loss of genome integrity. Generally, the maintenance of genomic stability depends significantly on the accurate regulation and timely repair of different genomic scales, ranging from DNA sequence to chromatin higher-order structures to chromosomes. Once irreversible damage and imperfect repair occurred, the resulting genomic instability can lead to a higher risk of tumorigenesis. However, how these factors disrupt genomic stability and their specific tumorigenic mechanisms remain unclear. Inspiringly, numerous studies have confirmed that long noncoding RNAs (lncRNAs), an important regulator of epigenetic inheritance, are functional in such process. Thus, this review aimed to discuss the vital factors that may lead to genomic instability at these multiple genomic scales, with an emphasis on the role of lncRNAs in it.

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