Mediator Complex Subunit 27-Enriched Small Extracellular Vesicles Mediate the Crosstalk between Periodontal Bacteria and HPV-Driven Head and Neck Cancer.

IF 3.6 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Tian Xu Qin, Wai Hoe Ng, Siew Kit Ng, Ying Ying Zhu, Min Fey Chek, Kai Dun Tang
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引用次数: 0

Abstract

It is well-documented in the literature that two well-known periodontal bacteria, Fusobacterium nucleatum and Porphyromonas gingivalis, play a pivotal role in regulating the cancer stemness properties of head and neck cancer (HNC); however, their role in human papillomavirus-driven HNC (HPV-driven HNC) remains unexplored. Here, we report for the first time that periodontal bacteria actively interplay with HPV-driven head and neck cancer stem cells (CSCs) via the activation of signaling pathways mediated by small extracellular vesicles (sEVs), leading to the rapid enrichment of CSCs during HPV-driven HNC progression and development. We observed an upregulation of Mediator Complex Subunit 27 (MED27) in sEVs derived from periodontal bacteria-infected HPV-driven HNC, as evidenced by 4D-microDIA quantitative proteomics analysis. Meanwhile, the silencing of MED27 resulted in the suppression of migratory, invasive, and sphere-forming abilities of HPV-driven HNC cells. Subsequent clinical data analysis revealed that the elevated level of MED27 was significantly correlated with aggressive clinicopathologic features and shorter survival in HNC patients. Most importantly, MED27 was expressed at a higher mRNA level in HPV-driven HNC patients when compared to controls and non-HPV-driven HNC patients, suggesting its potential as a diagnostic biomarker for HPV-driven HNC. This novel mechanistic insight could advance HPV-driven HNC diagnostic and therapeutic strategies.

中介复合物亚基27富集的细胞外小泡介导牙周细菌与hpv驱动的头颈癌之间的串扰。
文献充分证明,两种众所周知的牙周细菌,核梭杆菌和牙龈卟啉单胞菌,在头颈癌(HNC)的癌变特性调节中起关键作用;然而,它们在人乳头瘤病毒驱动的HNC (hpv驱动的HNC)中的作用仍未被探索。在这里,我们首次报道了牙周细菌通过激活由细胞外小泡(sev)介导的信号通路积极地与hpv驱动的头颈癌干细胞(CSCs)相互作用,导致在hpv驱动的HNC进展和发展过程中CSCs的快速富集。我们观察到,通过4D-microDIA定量蛋白质组学分析,在牙周细菌感染的hpv驱动的HNC衍生的sev中,介质复合物亚单位27 (MED27)上调。同时,MED27的沉默抑制了hpv驱动的HNC细胞的迁移、侵袭和成球能力。随后的临床数据分析显示,MED27水平升高与HNC患者侵袭性临床病理特征和较短的生存期显著相关。最重要的是,与对照组和非hpv驱动的HNC患者相比,MED27在hpv驱动的HNC患者中的mRNA表达水平更高,这表明它有可能作为hpv驱动的HNC的诊断生物标志物。这种新的机制见解可以推进hpv驱动的HNC诊断和治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Proteome Research
Journal of Proteome Research 生物-生化研究方法
CiteScore
9.00
自引率
4.50%
发文量
251
审稿时长
3 months
期刊介绍: Journal of Proteome Research publishes content encompassing all aspects of global protein analysis and function, including the dynamic aspects of genomics, spatio-temporal proteomics, metabonomics and metabolomics, clinical and agricultural proteomics, as well as advances in methodology including bioinformatics. The theme and emphasis is on a multidisciplinary approach to the life sciences through the synergy between the different types of "omics".
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