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靶向胆固醇依赖性的Piezo1激活会损害黑色素瘤细胞的阿米巴样迁移。

Targeting Cholesterol-Dependent Piezo1 Activation Impairs Amoeboid Migration in Melanoma Cells.

作者信息

Kuang Sylvia, Abrenica Alleah, Kar Neelakshi, Logue Jeremy S

机构信息

Department of Regenerative and Cancer Cell Biology, Albany Medical College, 47 New Scotland Ave, Albany, NY 12208.

出版信息

bioRxiv. 2025 Jul 17:2025.07.11.664494. doi: 10.1101/2025.07.11.664494.

Abstract

Bleb-based migration enables cancer cells to navigate the heterogeneous tumor microenvironment. Here, we report a phenotypic screen identifying drugs that inhibit bleb formation, a driver of amoeboid migration. Statins, including Fluvastatin and Pitavastatin, suppress amoeboid migration of melanoma cells in confined environments by reducing intracellular cholesterol. This disrupts plasma membrane tension sensing by Piezo1, lowering intracellular Ca levels. Both cholesterol supplementation and Piezo1 activation rescue migration in confined environments, confirming their functional link. Notably, high cholesterol biosynthesis enzyme levels correlate with reduced patient survival in melanoma. These findings reveal that cholesterol is essential for confinement sensing through Piezo1, identifying cholesterol biosynthesis or uptake as rational therapeutic targets against metastasis.

摘要

基于泡状伪足的迁移使癌细胞能够在异质性肿瘤微环境中导航。在此,我们报告了一项表型筛选,鉴定出抑制泡状伪足形成的药物,泡状伪足形成是变形虫样迁移的驱动因素。他汀类药物,包括氟伐他汀和匹伐他汀,通过降低细胞内胆固醇来抑制黑色素瘤细胞在受限环境中的变形虫样迁移。这破坏了Piezo1对质膜张力的感知,降低了细胞内钙离子水平。胆固醇补充和Piezo1激活均可挽救受限环境中的迁移,证实了它们之间的功能联系。值得注意的是,黑色素瘤患者中高胆固醇生物合成酶水平与生存率降低相关。这些发现表明,胆固醇对于通过Piezo1进行的受限感知至关重要,确定胆固醇生物合成或摄取作为抗转移的合理治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e019/12338549/2ac8b7c6da0f/nihpp-2025.07.11.664494v1-f0001.jpg

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