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长链非编码RNA在鼻咽癌放化疗抵抗中的作用

Role of long non-coding RNA in chemoradiotherapy resistance of nasopharyngeal carcinoma.

作者信息

Yang Yang, Yuan QuPing, Tang Weijian, Ma Ya, Duan JingYan, Yang GuoNing, Fang Yuan

机构信息

Otorhinolaryngology Head and Neck Surgery, Baoshan People's Hospital, Baoshan, Yunnan, China.

Puer People's Hospital, Department of Critical Medicine, PuEr, Yunnan, China.

出版信息

Front Oncol. 2024 Feb 29;14:1346413. doi: 10.3389/fonc.2024.1346413. eCollection 2024.

DOI:10.3389/fonc.2024.1346413
PMID:38487724
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10937456/
Abstract

Nasopharyngeal carcinoma (NPC) is a malignant tumor originating from the nasopharyngeal epithelial cells. Common treatment methods for NPC include radiotherapy, chemotherapy, and surgical intervention. Despite these approaches, the prognosis for NPC remains poor due to treatment resistance and recurrence. Hence, there is a crucial need for more comprehensive research into the mechanisms underlying treatment resistance in NPC. Long non coding RNAs (LncRNAs) are elongated RNA molecules that do not encode proteins. They paly significant roles in various biological processes within tumors, such as chemotherapy resistance, radiation resistance, and tumor recurrence. Recent studies have increasingly unveiled the mechanisms through which LncRNAs contribute to treatment resistance in NPC. Consequently, LncRNAs hold promise as potential biomarkers and therapeutic targets for diagnosing NPC. This review provides an overview of the role of LncRNAs in NPC treatment resistance and explores their potential as therapeutic targets for managing NPC.

摘要

鼻咽癌(NPC)是一种起源于鼻咽上皮细胞的恶性肿瘤。鼻咽癌的常见治疗方法包括放射治疗、化学治疗和手术干预。尽管有这些治疗方法,但由于治疗抵抗和复发,鼻咽癌的预后仍然很差。因此,迫切需要对鼻咽癌治疗抵抗的潜在机制进行更全面的研究。长链非编码RNA(LncRNAs)是不编码蛋白质的长链RNA分子。它们在肿瘤内的各种生物学过程中发挥重要作用,如化疗抵抗、放射抵抗和肿瘤复发。最近的研究越来越多地揭示了LncRNAs导致鼻咽癌治疗抵抗的机制。因此,LncRNAs有望成为诊断鼻咽癌的潜在生物标志物和治疗靶点。本综述概述了LncRNAs在鼻咽癌治疗抵抗中的作用,并探讨了它们作为治疗鼻咽癌靶点的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/546f/10937456/ff511730468e/fonc-14-1346413-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/546f/10937456/4c2335918794/fonc-14-1346413-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/546f/10937456/ff511730468e/fonc-14-1346413-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/546f/10937456/4c2335918794/fonc-14-1346413-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/546f/10937456/ff511730468e/fonc-14-1346413-g002.jpg

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本文引用的文献

1
Comprehensive analysis for the immune related biomarkers of platinum-based chemotherapy in ovarian cancer.卵巢癌铂类化疗免疫相关生物标志物的综合分析
Transl Oncol. 2023 Nov;37:101762. doi: 10.1016/j.tranon.2023.101762. Epub 2023 Aug 22.
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Current progress in immunotherapy of nasopharyngeal carcinoma.鼻咽癌免疫治疗的当前进展
Am J Cancer Res. 2023 Apr 15;13(4):1140-1147. eCollection 2023.
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Nasopharyngeal carcinoma ecology theory: cancer as multidimensional spatiotemporal "unity of ecology and evolution" pathological ecosystem.
鼻咽癌生态学理论:癌症作为多维时空的“生态与进化统一体”病理性生态系统。
Theranostics. 2023 Mar 5;13(5):1607-1631. doi: 10.7150/thno.82690. eCollection 2023.
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LncRNA CASC19: a novel oncogene involved in human cancer.长链非编码 RNA CASC19:一种参与人类癌症的新型癌基因。
Clin Transl Oncol. 2023 Oct;25(10):2841-2851. doi: 10.1007/s12094-023-03165-x. Epub 2023 Apr 7.
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Emerging role of non-coding RNAs in resistance to platinum-based anti-cancer agents in lung cancer.非编码RNA在肺癌对铂类抗癌药物耐药中的新作用
Front Pharmacol. 2023 Jan 26;14:1105484. doi: 10.3389/fphar.2023.1105484. eCollection 2023.
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LncRNA CASC19 Enhances the Radioresistance of Nasopharyngeal Carcinoma by Regulating the miR-340-3p/FKBP5 Axis.长链非编码 RNA CASC19 通过调节 miR-340-3p/FKBP5 轴增强鼻咽癌的放射抵抗性。
Int J Mol Sci. 2023 Feb 3;24(3):3047. doi: 10.3390/ijms24033047.
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lncRNA HOXA11-AS maintains the stemness of oral squamous cell carcinoma stem cells and reduces the radiosensitivity by targeting miR-518a-3p/PDK1.长链非编码RNA HOXA11-AS通过靶向miR-518a-3p/丙酮酸脱氢酶激酶1维持口腔鳞状细胞癌干细胞的干性并降低其放射敏感性。
J Oral Pathol Med. 2023 Mar;52(3):216-225. doi: 10.1111/jop.13405. Epub 2023 Feb 15.
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Nano Res. 2023;16(4):5357-5367. doi: 10.1007/s12274-022-5254-x. Epub 2023 Jan 3.
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Radiat Res. 2023 Feb 1;199(2):124-131. doi: 10.1667/RADE-22-00163.1.
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Front Immunol. 2022 Aug 12;13:969447. doi: 10.3389/fimmu.2022.969447. eCollection 2022.