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环状RNA翻译多肽在恶性肿瘤中的作用 被引量:1

Role of polypeptides translated by circular RNAs in malignant tumors
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摘要 作为特殊的非编码RNA,环状RNA(circular RNA,Circ RNA)是一种由pre-mRNA通过反式剪接形成的新型闭合环状的RNA分子。随着生物技术的飞速发展和研究的不断深入,对于CircRNA的鉴定和功能已有了新的认识。CircRNA由于缺乏5’帽子结构一直被认为不可翻译成蛋白质,已有证据表明其可通过核糖体内部进入位点(internal ribosomal entry site,IRES)和N6-甲基腺苷(N6-methyladenosine,m^(6)A)诱导的方式编码多肽,在多种恶性肿瘤的生物学行为中扮演重要角色。本文结合国内外研究,回顾CircRNA翻译多肽的可能机制,对其多肽产物在常见的恶性肿瘤中的功能及作用进行综述,探讨其可能存在的问题及潜在临床应用价值。 Circular RNAs(CircRNAs),as special non-coding RNAs,are novel closed-loop RNA molecules that are formed from pre-mRNAs by reverse splicing.The rapid development of biotechnology and increasing research have led to new insights into the identification and function of CircRNAs.CircRNAs have been considered to be untranslatable into proteins because of the lack of a 5’cap structure.However,some evidence has revealed that they can encode polypeptides via the internal ribosomal entry site and N6-methyladenosine(m^(6)A)induction and can play an important role in the biological behavior of various malignancies.Thus,in this review,using domestic and international research literature,we summarized the possible mechanisms of peptide translation by CircRNAs,assessed the functions and effects of peptide products in common malignant tumors,and discussed their possible problems and potential clinical applications.
作者 刘路政 武金才 Luzheng Liu;Jincai Wu(Department of Hepatobiliary and Pancreatic Surgery,Hainan Affiliated Hospital of Hainan Medical University(Hainan General Hospital),Haikou 570311,China)
出处 《中国肿瘤临床》 CAS CSCD 北大核心 2022年第1期31-36,共6页 Chinese Journal of Clinical Oncology
基金 国家自然科学基金项目(编号:81660489) 海南省研究生创新科研项目(编号:Hys2020-355) 海南省重点研发计划项目(编号:ZDYF2020134)资助。
关键词 环状RNA 翻译 恶性肿瘤 非编码RNA circular RNA(CircRNA) translation malignant tumor non-coding RNA
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  • 1Hansen TB, Jensen TI, Clausen BH, et aL Nature 2013; 495:384-388.
  • 2Jeck WR, Sorrentino JA, Wang K, et al. RNA 2013; 19:141-157.
  • 3Memczak S, Jens M, Elefsinioti A, et al. Nature 2013; 495:333-338.
  • 4Salzman J, Gawad C, Wang PL, et al. PIoS One 2012; 7:e30733.
  • 5Salzman J, Chen RE, Olsen MN, et al. PLoS Genet 2013; 9:e1003777.
  • 6Pant S, Hilton H, Burczynski ME. Biochem Pharmaco12012; 83:1484- 1494.
  • 7Pruitt KD, Tatusova T, Brown GR, et al. Nucleic Acids Res 2012; 40:D130-D135.
  • 8Xiao-Li Ping,Bao-Fa Sun,Lu Wang,Wen Xiao,Xin Yang,Wen-Jia Wang,Samir Adhikari,Yue Shi,Ying Lv,Yu-Sheng Chen,Xu Zhao,Ang Li,Ying Yang,Ujwal Dahal,Xiao-Min Lou,Xi Liu,Jun Huang,Wei-Ping Yuan,Xiao-Fan Zhu,Tao Cheng,Yong-Liang Zhao,Xinquan Wang,Jannie M Rendtlew Danielsen,Feng Liu,Yun-Gui Yang.Mammalian WTAP is a regulatory subunit of the RNA N6-methyladenosine methyltransferase[J].Cell Research,2014,24(2):177-189. 被引量:303
  • 9Hailing Shi,Xiao Wang,Zhike Lu,Boxuan S Zhao,Honghui Ma,Phillip J HSU,Chang Liu,Chuan He.YTHDF3 facilitates translation and decay of N6-methyladenosine-modified RNA[J].Cell Research,2017,27(3):315-328. 被引量:209
  • 10Ang Li,Yu-Sheng Chen,Xiao-Li Ping,Xin Yang,Wen Xiao,Ying Yang,Hui-Ying Sun,Qin Zhu,Poonam Baidya,Xing Wang,Devi Prasad Bhattarai,Yong-Liang Zhao,Bao-Fa Sun,Yun-Gui Yang.Cytoplasmic m6A reader YTHDF3 promotes mRNA translation[J].Cell Research,2017,27(3):444-447. 被引量:104

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