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染色体不稳定性驱动的癌症进展:与肿瘤微环境的相互作用和治疗策略。

Chromosomal Instability-Driven Cancer Progression: Interplay with the Tumour Microenvironment and Therapeutic Strategies.

机构信息

European Research Institute for the Biology of Ageing (ERIBA), University Groningen, University Medical Center Groningen, 9713 AV Groningen, The Netherlands.

Department of Research in Sexual and Reproductive Health, Gorgas Memorial Institute for Health Studies, Panama City 0816-02593, Panama.

出版信息

Cells. 2023 Nov 26;12(23):2712. doi: 10.3390/cells12232712.


DOI:10.3390/cells12232712
PMID:38067140
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10706135/
Abstract

Chromosomal instability (CIN) is a prevalent characteristic of solid tumours and haematological malignancies. CIN results in an increased frequency of chromosome mis-segregation events, thus yielding numerical and structural copy number alterations, a state also known as aneuploidy. CIN is associated with increased chances of tumour recurrence, metastasis, and acquisition of resistance to therapeutic interventions, and this is a dismal prognosis. In this review, we delve into the interplay between CIN and cancer, with a focus on its impact on the tumour microenvironment-a driving force behind metastasis. We discuss the potential therapeutic avenues that have resulted from these insights and underscore their crucial role in shaping innovative strategies for cancer treatment.

摘要

染色体不稳定(CIN)是实体瘤和血液恶性肿瘤的普遍特征。CIN 导致染色体错误分离事件的频率增加,从而产生数值和结构的拷贝数改变,这种状态也称为非整倍体。CIN 与肿瘤复发、转移和获得治疗干预耐药的机会增加有关,这是一个预后不良的情况。在这篇综述中,我们深入探讨了 CIN 与癌症之间的相互作用,重点关注其对肿瘤微环境的影响——这是转移的驱动力。我们讨论了这些见解带来的潜在治疗途径,并强调了它们在塑造癌症治疗创新策略中的关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63db/10706135/8e18fd8a3dfa/cells-12-02712-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63db/10706135/5645d9c3c1ea/cells-12-02712-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63db/10706135/8e18fd8a3dfa/cells-12-02712-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63db/10706135/5645d9c3c1ea/cells-12-02712-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63db/10706135/8e18fd8a3dfa/cells-12-02712-g002.jpg

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[1]
Chromosomal Instability-Driven Cancer Progression: Interplay with the Tumour Microenvironment and Therapeutic Strategies.

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[8]
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本文引用的文献

[1]
Non-cell-autonomous cancer progression from chromosomal instability.

Nature. 2023-8

[2]
Human STING is a proton channel.

Science. 2023-8-4

[3]
Cancer chemotherapy and beyond: Current status, drug candidates, associated risks and progress in targeted therapeutics.

Genes Dis. 2022-3-18

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Differential Protein and Glycan Packaging into Extracellular Vesicles in Response to 3D Gastric Cancer Cellular Organization.

Adv Sci (Weinh). 2023-8

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Epigenetic dysregulation from chromosomal transit in micronuclei.

Nature. 2023-7

[6]
Classifying cGAS-STING Activity Links Chromosomal Instability with Immunotherapy Response in Metastatic Bladder Cancer.

Cancer Res Commun. 2022-8

[7]
cGAS-STING signalling in cancer: striking a balance with chromosomal instability.

Biochem Soc Trans. 2023-4-26

[8]
Harnessing transcriptionally driven chromosomal instability adaptation to target therapy-refractory lethal prostate cancer.

Cell Rep Med. 2023-2-21

[9]
Loss of RanGAP1 drives chromosome instability and rapid tumorigenesis of osteosarcoma.

Dev Cell. 2023-2-6

[10]
Current understanding of the cGAS-STING signaling pathway: Structure, regulatory mechanisms, and related diseases.

Zool Res. 2023-1-18

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