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那些杀不死你的,会使你变得更强大:通过细胞骨架重塑和肌球蛋白II重新激活在抗癌治疗中存活下来。

What does not kill you makes you stronger: surviving anti-cancer therapies by cytoskeletal remodeling and Myosin II reactivation.

作者信息

Orgaz Jose L, Sanz-Moreno Victoria

机构信息

Barts Cancer Institute, Queen Mary University of London, John Vane Science Building, London, UK.

Facultad de Ciencias Experimentales, Universidad Francisco de Vitoria, Madrid, Spain.

出版信息

Mol Cell Oncol. 2020 Mar 26;7(3):1735911. doi: 10.1080/23723556.2020.1735911. eCollection 2020.

DOI:10.1080/23723556.2020.1735911
PMID:32391428
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7199747/
Abstract

Myosin II and its regulator Rho-associated coiled-coil containing protein kinase (ROCK) are essential for cell invasion and metastatic dissemination. Our recent findings show that this molecular machinery is also involved in drug resistance in melanoma by playing a dual role: protection of tumor cells from reactive oxygen species (ROS) and DNA damage (intrinsic), and co-option of myeloid and lymphoid populations to establish immunosuppression (extrinsic).

摘要

肌球蛋白II及其调节因子Rho相关卷曲螺旋蛋白激酶(ROCK)对于细胞侵袭和转移扩散至关重要。我们最近的研究结果表明,这种分子机制在黑色素瘤的耐药性中也发挥着双重作用:保护肿瘤细胞免受活性氧(ROS)和DNA损伤(内在作用),以及利用髓系和淋巴细胞群体建立免疫抑制(外在作用)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/398c/7199747/902104bac03e/kmco-07-03-1735911-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/398c/7199747/902104bac03e/kmco-07-03-1735911-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/398c/7199747/902104bac03e/kmco-07-03-1735911-g001.jpg

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本文引用的文献

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Myosin II Reactivation and Cytoskeletal Remodeling as a Hallmark and a Vulnerability in Melanoma Therapy Resistance.肌球蛋白 II 的重新激活和细胞骨架重塑作为黑色素瘤治疗耐药性的标志和弱点。
Cancer Cell. 2020 Jan 13;37(1):85-103.e9. doi: 10.1016/j.ccell.2019.12.003.
2
Regional Activation of Myosin II in Cancer Cells Drives Tumor Progression via a Secretory Cross-Talk with the Immune Microenvironment.肌球蛋白 II 在癌细胞中的区域激活通过与免疫微环境的分泌串扰推动肿瘤进展。
Cell. 2019 Feb 7;176(4):757-774.e23. doi: 10.1016/j.cell.2018.12.038. Epub 2019 Jan 31.
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Delivery of Protein Kinase A by CRISPRMAX and Its Effects on Breast Cancer Stem-Like Properties.通过CRISPRMAX递送蛋白激酶A及其对乳腺癌干细胞样特性的影响。
Pharmaceutics. 2020 Dec 23;13(1):11. doi: 10.3390/pharmaceutics13010011.
多重免疫组化准确定义转移性黑色素瘤的免疫背景。
Sci Rep. 2018 Jul 24;8(1):11158. doi: 10.1038/s41598-018-28944-3.
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A Convergence-Based Framework for Cancer Drug Resistance.基于融合的癌症药物耐药性研究框架
Cancer Cell. 2018 May 14;33(5):801-815. doi: 10.1016/j.ccell.2018.03.025.
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PD-1 expression by tumour-associated macrophages inhibits phagocytosis and tumour immunity.肿瘤相关巨噬细胞的PD-1表达抑制吞噬作用和肿瘤免疫。
Nature. 2017 May 25;545(7655):495-499. doi: 10.1038/nature22396. Epub 2017 May 17.
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Primary, Adaptive, and Acquired Resistance to Cancer Immunotherapy.癌症免疫疗法的原发性、适应性和获得性耐药性。
Cell. 2017 Feb 9;168(4):707-723. doi: 10.1016/j.cell.2017.01.017.
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Genomic and Transcriptomic Features of Response to Anti-PD-1 Therapy in Metastatic Melanoma.转移性黑色素瘤中抗PD-1治疗反应的基因组和转录组特征
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