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结直肠癌中的自噬相关长链非编码RNA和外泌体长链非编码RNA:聚焦于长链非编码RNA靶向策略

Autophagy-related lncRNAs and exosomal lncRNAs in colorectal cancer: focusing on lncRNA-targeted strategies.

作者信息

Dong Yan, He Yiwei, Geng Yanna, Wei Meimei, Zhou Xiaomei, Lian Jianlun, Hallajzadeh Jamal

机构信息

The First Affiliated Hospital of Hebei University of Chinese Medicine, Shijiazhuang, 050011, Hebei, China.

Department of Biochemistry and Nutrition, Research Center for Evidence-Based Health Management, Maragheh University of Medical Sciences, Maragheh, Iran.

出版信息

Cancer Cell Int. 2024 Sep 28;24(1):328. doi: 10.1186/s12935-024-03503-1.

DOI:10.1186/s12935-024-03503-1
PMID:39342235
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11439232/
Abstract

Autophagy is a cellular process that involves the degradation and recycling of cellular components, including damaged proteins and organelles. It is an important mechanism for maintaining cellular homeostasis and has been implicated in various diseases, including cancer. Long non-coding RNAs (lncRNAs) are a class of RNA molecules that do not code for proteins but instead play regulatory roles in gene expression. Emerging evidence suggests that lncRNAs can influence autophagy and contribute to the development and progression of colorectal cancer (CRC). Several lncRNAs have been identified as key players in modulating autophagy in CRC. The dysregulation of autophagy and non-coding RNAs (ncRNAs) in CRC suggests a complex interplay between these two factors in the pathogenesis of the disease. Modulating autophagy may sensitize cancer cells to existing therapies or improve the efficacy of new treatment approaches. Additionally, targeting specific lncRNAs involved in autophagy regulation could potentially be used as a therapeutic intervention to inhibit tumor growth, metastasis, and overcome drug resistance in CRC. In this review, a thorough overview is presented, encompassing the functions and underlying mechanisms of autophagy-related lncRNAs in a range of critical areas within tumor biology. These include cell proliferation, apoptosis, migration, invasion, drug resistance, angiogenesis, and radiation resistance.

摘要

自噬是一种细胞过程,涉及细胞成分的降解和再循环,包括受损的蛋白质和细胞器。它是维持细胞稳态的重要机制,并与包括癌症在内的各种疾病有关。长链非编码RNA(lncRNA)是一类不编码蛋白质但在基因表达中起调节作用的RNA分子。新出现的证据表明,lncRNA可以影响自噬,并促进结直肠癌(CRC)的发生和发展。几种lncRNA已被确定为CRC中调节自噬的关键因子。CRC中自噬和非编码RNA(ncRNA)的失调表明这两个因素在疾病发病机制中存在复杂的相互作用。调节自噬可能会使癌细胞对现有疗法敏感,或提高新治疗方法的疗效。此外,靶向参与自噬调节的特定lncRNA可能被用作一种治疗干预措施,以抑制CRC中的肿瘤生长、转移和克服耐药性。在这篇综述中,我们对肿瘤生物学一系列关键领域中自噬相关lncRNA的功能和潜在机制进行了全面概述。这些领域包括细胞增殖、凋亡、迁移、侵袭、耐药性、血管生成和辐射抗性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c976/11439232/af192744788a/12935_2024_3503_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c976/11439232/4777e7b7cddf/12935_2024_3503_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c976/11439232/a5f0839229f7/12935_2024_3503_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c976/11439232/0ae88f4d6808/12935_2024_3503_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c976/11439232/af192744788a/12935_2024_3503_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c976/11439232/4777e7b7cddf/12935_2024_3503_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c976/11439232/a5f0839229f7/12935_2024_3503_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c976/11439232/0ae88f4d6808/12935_2024_3503_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c976/11439232/af192744788a/12935_2024_3503_Fig4_HTML.jpg

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本文引用的文献

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Autophagy: Regulator of cell death.自噬:细胞死亡的调控者。
Cell Death Dis. 2023 Oct 4;14(10):648. doi: 10.1038/s41419-023-06154-8.
2
Autophagy-related lncRNAs in tumor progression and drug resistance: A double-edged sword.肿瘤进展和耐药性中与自噬相关的长链非编码RNA:一把双刃剑
Genes Dis. 2023 Jun 16;11(1):367-381. doi: 10.1016/j.gendis.2023.04.015. eCollection 2024 Jan.
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The mitophagy pathway and its implications in human diseases.自噬途径及其在人类疾病中的意义。
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Decoding colorectal cancer targeted therapy: a bibliometric journey of the last decade (2015-2024).解读结直肠癌靶向治疗:过去十年(2015 - 2024年)的文献计量学历程
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CAF-derived exosomal lncRNA FAL1 promotes chemoresistance to oxaliplatin by regulating autophagy in colorectal cancer.CAF 来源的外泌体 lncRNA FAL1 通过调控自噬促进结直肠癌细胞对奥沙利铂的耐药性。
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MYC-activated CERS6-AS1 sponges miR-6838-5p and regulates the expression of RUBCNL in colorectal cancer.MYC 激活的 CERS6-AS1 通过海绵吸附 miR-6838-5p 调控结直肠癌中 RUBCNL 的表达。
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Molecular mechanism of Streptococcus pneumoniae-targeting xenophagy recognition and evasion: Reinterpretation of pneumococci as intracellular bacteria.肺炎链球菌靶向异噬作用识别和逃避的分子机制:将肺炎球菌重新解读为胞内菌。
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Autophagy and autophagy-related pathways in cancer.自噬和癌症中的自噬相关途径。
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