Autophagy-related lncRNAs in tumor progression and drug resistance: A double-edged sword

被引:20
作者
Zhang, Yunchao [1 ]
Tang, Jiayu [1 ]
Wang, Cheng [3 ]
Zhang, Qinxiu [1 ]
Zeng, Anqi [2 ]
Song, Linjiang [1 ]
机构
[1] Chengdu Univ Tradit Chinese Med, Sch Med & Life Sci, Chengdu 611137, Sichuan, Peoples R China
[2] Sichuan Acad Chinese Med Sci, Inst Translat Pharmacol & Clin Applicat, Chengdu 610041, Sichuan, Peoples R China
[3] Chengdu Univ Tradit Chinese Med, Sch Pharm, Chengdu 611137, Sichuan, Peoples R China
关键词
Apoptosis; Autophagy; Biomarker; Cancer; Drug resistance; LncRNA; LUNG-CANCER CELLS; COLORECTAL-CANCER; INHIBITING AUTOPHAGY; COLON-CANCER; CISPLATIN-RESISTANCE; UCA1; CONTRIBUTES; OVARIAN-CANCER; PROMOTES; RNA; PROLIFERATION;
D O I
10.1016/j.gendis.2023.04.015
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The incidence and mortality rates of cancer are increasing every year worldwide but the survival rate of cancer patients is still unsatisfactory. Therefore, it is necessary to further elucidate the molecular mechanisms involved in tumor development and drug resis-tance to improve cancer cure or survival rates. In recent years, autophagy has become a hot topic in the field of oncology research, which plays a double-edged role in tumorigenesis, pro-gression, and drug resistance. Meanwhile, long non-coding RNA (lncRNA) has also been shown to regulate autophagy, and the two-sided nature of autophagy determines the dual regulatory role of autophagy-related lncRNAs (ARlncRNAs). Therefore, ARlncRNAs can be effective ther-apeutic targets for various cancers. Furthermore, the high abundance and stability of ARlncR-NAs in tumor tissues make them promising biomarkers. In this review, we summarized the roles and mechanisms of ARlncRNAs in tumor cell proliferation, apoptosis, migration, invasion, drug resistance, angiogenesis, radiation resistance, and immune regulation. In addition, we described the clinical significance of these ARlncRNAs, including as biomarkers/therapeutic targets and their association with clinical drugs. & COPY; 2023 The Authors. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co., Ltd. This is an open access article under the CC BY license (http://creativecommons.org/ licenses/by/4.0/).
引用
收藏
页码:367 / 381
页数:15
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