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肿瘤相关外泌体在癌症进展及治疗靶点中的作用

Tumor-associated exosomes in cancer progression and therapeutic targets.

作者信息

Liu Xiaomin, Wu Fan, Pan Wei, Liu Guangchao, Zhang Hui, Yan Dawei, Zheng Saijing, Ma Zhongliang, Ren Xiaojun

机构信息

Lab for Noncoding RNA & Cancer School of Life Sciences Shanghai University Shanghai China.

Shanghai New Tobacco Product Research Institute Co., Ltd. Shanghai China.

出版信息

MedComm (2020). 2024 Sep 7;5(9):e709. doi: 10.1002/mco2.709. eCollection 2024 Sep.


DOI:10.1002/mco2.709
PMID:39247621
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11380050/
Abstract

Exosomes are small membrane vesicles that are released by cells into the extracellular environment. Tumor-associated exosomes (TAEs) are extracellular vesicles that play a significant role in cancer progression by mediating intercellular communication and contributing to various hallmarks of cancer. These vesicles carry a cargo of proteins, lipids, nucleic acids, and other biomolecules that can be transferred to recipient cells, modifying their behavior and promoting tumor growth, angiogenesis, immune modulation, and drug resistance. Several potential therapeutic targets within the TAEs cargo have been identified, including oncogenic proteins, miRNAs, tumor-associated antigens, immune checkpoint proteins, drug resistance proteins, and tissue factor. In this review, we will systematically summarize the biogenesis, composition, and function of TAEs in cancer progression and highlight potential therapeutic targets. Considering the complexity of exosome-mediated signaling and the pleiotropic effects of exosome cargoes has challenge in developing effective therapeutic strategies. Further research is needed to fully understand the role of TAEs in cancer and to develop effective therapies that target them. In particular, the development of strategies to block TAEs release, target TAEs cargo, inhibit TAEs uptake, and modulate TAEs content could provide novel approaches to cancer treatment.

摘要

外泌体是细胞释放到细胞外环境中的小膜泡。肿瘤相关外泌体(TAEs)是细胞外囊泡,通过介导细胞间通讯并促成癌症的各种特征,在癌症进展中发挥重要作用。这些囊泡携带蛋白质、脂质、核酸和其他生物分子的货物,可转移到受体细胞,改变其行为并促进肿瘤生长、血管生成、免疫调节和耐药性。已确定TAEs货物中的几个潜在治疗靶点,包括致癌蛋白、微小RNA、肿瘤相关抗原、免疫检查点蛋白、耐药蛋白和组织因子。在本综述中,我们将系统总结TAEs在癌症进展中的生物发生、组成和功能,并突出潜在的治疗靶点。考虑到外泌体介导的信号传导的复杂性以及外泌体货物的多效性效应,在开发有效的治疗策略方面具有挑战性。需要进一步研究以充分了解TAEs在癌症中的作用,并开发针对它们的有效疗法。特别是,阻断TAEs释放、靶向TAEs货物、抑制TAEs摄取和调节TAEs内容物的策略的开发可为癌症治疗提供新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/488a/11380050/d63cc8f7b002/MCO2-5-e709-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/488a/11380050/041fa8196404/MCO2-5-e709-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/488a/11380050/97edcbd74f0c/MCO2-5-e709-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/488a/11380050/d63cc8f7b002/MCO2-5-e709-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/488a/11380050/041fa8196404/MCO2-5-e709-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/488a/11380050/97edcbd74f0c/MCO2-5-e709-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/488a/11380050/d63cc8f7b002/MCO2-5-e709-g003.jpg

相似文献

[1]
Tumor-associated exosomes in cancer progression and therapeutic targets.

MedComm (2020). 2024-9-7

[2]
Protein cargo in extracellular vesicles as the key mediator in the progression of cancer.

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[3]
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[4]
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[5]
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Biochim Biophys Acta Rev Cancer. 2021-1

[6]
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[7]
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[8]
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Med Oncol. 2021-3-20

[9]
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Cancer Drug Resist. 2020-3-19

[10]
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Int J Mol Sci. 2023-12-23

引用本文的文献

[1]
A LncRNA panel within EpCAM-specific exosomes for noninvasive early diagnosing non-small cell lung cancer.

Respir Res. 2025-4-13

本文引用的文献

[1]
The activity and immune dynamics of PD-1 inhibition on high-risk pulmonary ground glass opacity lesions: insights from a single-arm, phase II trial.

Signal Transduct Target Ther. 2024-4-19

[2]
Global cancer statistics: A healthy population relies on population health.

CA Cancer J Clin. 2024

[3]
Knockdown of liver cancer cell-secreted exosomal PSMA5 controls macrophage polarization to restrain cancer progression by blocking JAK2/STAT3 signaling.

Immun Inflamm Dis. 2024-2

[4]
Cancer statistics, 2024.

CA Cancer J Clin. 2024

[5]
Exploring the roles and molecular mechanisms of RNA binding proteins in the sorting of noncoding RNAs into exosomes during tumor progression.

J Adv Res. 2024-11

[6]
Hypoxic tumour-derived exosomal miR-1225-5p regulates M2 macrophage polarisation via toll-like receptor 2 to promote ovarian cancer progress.

Autoimmunity. 2023-12

[7]
Exosome derived from tumor-associated macrophages: biogenesis, functions, and therapeutic implications in human cancers.

Biomark Res. 2023-11-19

[8]
Intervening in hnRNPA2B1-mediated exosomal transfer of tumor-suppressive miR-184-3p for tumor microenvironment regulation and cancer therapy.

J Nanobiotechnology. 2023-11-14

[9]
miRNAs and exosomal miRNAs in lung cancer: New emerging players in tumor progression and therapy response.

Pathol Res Pract. 2023-11

[10]
Visual genetic typing of glioma using proximity-anchored in situ spectral coding amplification.

Exploration (Beijing). 2023-7-6

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