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The role and mechanism of long non-coding RNAs in homologous recombination repair of radiation-induced DNA damage
Authors:Nanxi Yu  Hongran Qin  Fangxiao Zhang  Tingting Liu  Kun Cao  Yanyong Yang  Yuanyuan Chen  Jianming Cai
Institution:1. School of Public Health and Management, Wenzhou Medical University, University Town, Wenzhou, China

South Zhejiang Institute of Radiation Medicine and Nuclear Technology, Wenzhou, China;2. Department of Nuclear Radiation, Shanghai Pulmonary Hospital,School of Medicine, Tongji University, Shanghai, China;3. School of Public Health and Management, Wenzhou Medical University, University Town, Wenzhou, China;4. Department of Radiation Medicine, Faculty of Naval Medicine, Naval Medical University, Shanghai, China;5. South Zhejiang Institute of Radiation Medicine and Nuclear Technology, Wenzhou, China

Abstract:DNA double-strand breaks can seriously damage the genetic information that organisms depend on for survival and reproduction. Therefore, cells require a robust DNA damage response mechanism to repair the damaged DNA. Homologous recombination (HR) allows error-free repair, which is key to maintaining genomic integrity. Long non-coding RNAs (lncRNAs) are RNA molecules that are longer than 200 nucleotides. In recent years, a number of studies have found that lncRNAs can act as regulators of gene expression and DNA damage response mechanisms, including HR repair. Moreover, they have significant effects on the occurrence, development, invasion and metastasis of tumor cells, as well as the sensitivity of tumors to radiotherapy and chemotherapy. These studies have therefore begun to expose the great potential of lncRNAs for clinical applications. In this review, we focus on the regulatory roles of lncRNAs in HR repair.
Keywords:DNA damage response  homologous recombination  ionizing radiation  lncRNAs
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