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辅酶 Q 和 UBIAD1 使癌细胞变硬,调节乳腺癌中的细胞外基质信号和铁死亡。

Cancer cell stiffening via CoQ and UBIAD1 regulates ECM signaling and ferroptosis in breast cancer.

机构信息

Laboratory of Angiogenesis and Cancer Metabolism, Department of Biology, University of Padova, Padova, Italy.

Immunology and Molecular Oncology Unit, Veneto Institute of Oncology IOV - IRCCS, Padova, Italy.

出版信息

Nat Commun. 2024 Sep 18;15(1):8214. doi: 10.1038/s41467-024-52523-y.

Abstract

CoQ (Coenzyme Q) is an essential fat-soluble metabolite that plays a key role in cellular metabolism. A less-known function of CoQ is whether it may act as a plasma membrane-stabilizing agent and whether this property can affect cancer development and progression. Here, we show that CoQ and its biosynthetic enzyme UBIAD1 play a critical role in plasmamembrane mechanical properties that are of interest for breast cancer (BC) progression and treatment. CoQ and UBIAD1 increase membrane fluidity leading to increased cell stiffness in BC. Furthermore, CoQ and UBIAD1 states impair ECM (extracellular matrix)-mediated oncogenic signaling and reduce ferroptosis resistance in BC settings. Analyses on human patients and mouse models reveal that UBIAD1 loss is associated with BC development and progression and UBIAD1 expression in BC limits CTCs (circulating tumor cells) survival and lung metastasis formation. Overall, this study reveals that CoQ and UBIAD1 can be further investigated to develop therapeutic interventions to treat BC patients with poor prognosis.

摘要

辅酶 Q(CoQ)是一种必需的脂溶性代谢物,在细胞代谢中起着关键作用。辅酶 Q 的一个鲜为人知的功能是,它是否可以作为质膜稳定剂,以及这种特性是否会影响癌症的发展和进展。在这里,我们表明辅酶 Q 及其生物合成酶 UBIAD1 在质膜机械性能方面发挥着关键作用,这些性能与乳腺癌(BC)的进展和治疗有关。辅酶 Q 和 UBIAD1 增加了膜的流动性,导致 BC 中的细胞硬度增加。此外,辅酶 Q 和 UBIAD1 状态会损害 ECM(细胞外基质)介导的致癌信号,并降低 BC 环境中的铁死亡抗性。对人类患者和小鼠模型的分析表明,UBIAD1 的缺失与 BC 的发展和进展有关,而 BC 中的 UBIAD1 表达会限制 CTCs(循环肿瘤细胞)的存活和肺转移的形成。总的来说,这项研究表明,辅酶 Q 和 UBIAD1 可以进一步研究,以开发治疗干预措施,治疗预后不良的 BC 患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72eb/11410950/35a50d2de154/41467_2024_52523_Fig1_HTML.jpg

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