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中国临床研究:2022,35(11):1489-1492
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非编码RNA编码的蛋白质/多肽在胃肠肿瘤发生发展中作用的研究进展
(南京医科大学第二附属医院肿瘤科,江苏 南京 210011)
Research progress on the role of protein/polypeptide encoded by non-coding RNA in the genesis and development of gastrointestinal tumors
(Department of Oncology, The Second Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu 210011, China)
摘要
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投稿时间:2022-08-08   网络发布日期:2022-11-20
中文摘要: 胃肠肿瘤是迄今为止最常见的恶性肿瘤,也是全球癌症相关死亡的最常见原因。尽管目前胃肠肿瘤的研究已经取得了重大进展,但与其发生发展相关的分子机制仍有待进一步探索。传统观点认为非编码RNA(ncRNAs)不具有编码功能,然而近年来的研究表明ncRNAs中的少数小型开放阅读框(sORF)实际上具有编码肽或蛋白质的潜力。如长链非编码RNA(lncRNA)、环状RNA(circRNA)和初级miRNA(pri-miRNA)含有的开放阅读框(ORFs)具有编码多肽或蛋白质的能力,且这些多肽能够调控癌细胞的生理活动,影响肿瘤的发生发展过程。本综述的重点是阐述lncRNA、circRNA和pri-miRNA编码的蛋白质或多肽在胃肠肿瘤发生发展中作用的研究进展,以促进发现更多由ncRNAs编码的功能肽或蛋白质,并进一步开发新的抗癌治疗靶点及诊断和预后肿瘤标志物。
Abstract:Gastrointestinal tumor is the most common malignant tumor and the most common cause of cancer-related death worldwide. Although great progress has been made in the research of gastrointestinal tumors, the molecular mechanisms related to their occurrence and development still need to be further explored. The traditional view is that non-coding RNAs(ncRNAs) do not have coding functions. However, recent studies have shown that a small number of small open reading frames(sORF) in ncRNAs actually have the potential to encode peptides or proteins. For example, the open reading frames(ORFs) contained in lncRNA, circRNA and pri-miRNAs have the ability to encode polypeptides or proteins, and these polypeptides can regulate the physiological activities of cancer cells and affect the occurrence and development of tumors. The review is to declare the research progress on the role of proteins or polypeptides encoded by lncRNAs, circRNAs and pri-miRNAs in the genesis and development of gastrointestinal tumors, so as to promote the discovery of more functional peptides or proteins encoded by〖KG)〗 ncRNAs, and further develop new anticancer therapeutic targets and diagnostic and prognostic tumor markers.
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引用文本:
王科明.非编码RNA编码的蛋白质/多肽在胃肠肿瘤发生发展中作用的研究进展[J].中国临床研究,2022,35(11):1489-1492.

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