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Exosomal non-coding RNAs: Blueprint in colorectal cancer metastasis and therapeutic targets

转移 微泡 小RNA 结直肠癌 生物 癌症研究 癌症 长非编码RNA 外体 非编码RNA 生物信息学 医学 基因 核糖核酸 遗传学
作者
Bashdar Mahmud Hussen,Sara Tharwat Abdullah,Snur Rasool Abdullah,Yousif Mohammed Younis,Hazha Jamal Hidayat,Mohammed Fatih Rasul,Sayran Mohamadtahr
出处
期刊:Non-coding RNA Research [Elsevier BV]
卷期号:8 (4): 615-632 被引量:6
标识
DOI:10.1016/j.ncrna.2023.09.001
摘要

Colorectal cancer (CRC) is ranked as the world's third-most prevalent cancer, and metastatic CRC considerably increases cancer-related fatalities globally. A number of complex mechanisms that are strictly controlled at the molecular level are involved in metastasis, which is the primary reason for death in people with CRC. Recently, it has become clear that exosomes, which are small extracellular vesicles released by non-tumorous and tumorigenic cells, play a critical role as communication mediators among tumor microenvironment (TME). To facilitate communication between the TME and cancer cells, non-coding RNAs (ncRNAs) play a crucial role and are recognized as potent regulators of gene expression and cellular processes, such as metastasis and drug resistance. NcRNAs are now recognized as potent regulators of gene expression and many hallmarks of cancer, including metastasis. Exosomal ncRNAs, like miRNAs, circRNAs, and lncRNAs, have been demonstrated to influence a number of cellular mechanisms that contribute to CRC metastasis. However, the molecular mechanisms that link exosomal ncRNAs with CRC metastasis are not well understood. This review highlights the essential roles that exosomal ncRNAs play in the progression of CRC metastatic disease and explores the therapeutic choices that are open to patients who have CRC metastases. However, exosomal ncRNA treatment strategy development is still in its early phases; consequently, additional investigation is required to improve delivery methods and find novel therapeutic targets as well as confirm the effectiveness and safety of these therapies in preclinical and clinical contexts.

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