Enterococcus faecalis co-cultured with oral cancer cells exhibits higher virulence and promotes cancer cell survival, proliferation, and migration: an in vitro study.

Fida Fathima, Yuvarajan Subramaniyan, Akshatha Rai, Punchappady Devasya Rekha
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Abstract

Introduction. Enterococcus faecalis is a common pathogen associated with many oral diseases and is often isolated from oral cancer patients. However, limited information is available on its key virulence gene expression in oral cancer cell microenvironment and cancer cell behaviour in co-culture studies.Hypothesis. E. faecalis overexpresses virulence genes when co-cultured with oral cancer cells and possibly alters the tumour microenvironment, promoting oral cancer proliferation and survival.Aim. To investigate altered virulence gene expression in E. faecalis and oral cancer cell behaviour using in vitro co-culture experiments.Methodology. Cal27 cells were co-cultured with E. faecalis and assessed for their cell proliferation, apoptosis, migration and clonogenicity using standard cell culture assays. The levels of reactive oxygen species (ROS) and inflammatory cytokines, along with proliferative, angiogenic and apoptotic biomarker expressions, were also assessed. E. faecalis adherence to cancer cells was demonstrated by the gentamicin protection assay. Real time-PCR was used to analyse the expression of virulence genes.Results. Co-culture of Cal27 cells with E. faecalis showed significantly higher cell proliferation, migration and clonogenicity compared to the control (P<0.01). A significant increase in the levels of ROS and inflammatory cytokines and overexpression of Ki67, vascular endothelial growth factor, extracellular signal-regulated kinase 1/2, phosphoinositide 3 kinase and Akt was observed in the co-culture group. E. faecalis also downregulated p53 and Bax genes while upregulated Bcl-2. The virulence genes GelE, Asa and Ace were overexpressed in E. faecalis co-cultured with Cal27 cells.Conclusion. The results from this study indicate the possible risks of E. faecalis infection in oral cancer. An effective antibiotic strategy against E. faecalis to prevent complications associated with oral diseases, including cancer, is needed.

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与口腔癌细胞共同培养的粪肠球菌具有更强的毒力,并能促进癌细胞存活、增殖和迁移:一项体外研究。
导言。粪肠球菌是一种与多种口腔疾病相关的常见病原体,经常从口腔癌患者体内分离出来。然而,关于其关键毒力基因在口腔癌细胞微环境中的表达以及癌细胞在共培养研究中的行为的信息却很有限。假设:当粪大肠杆菌与口腔癌细胞共培养时,它会过度表达毒力基因,并可能改变肿瘤微环境,促进口腔癌的增殖和存活。利用体外共培养实验研究粪肠球菌的毒力基因表达和口腔癌细胞行为的改变。将 Cal27 细胞与粪大肠杆菌共培养,并使用标准细胞培养试验评估其细胞增殖、凋亡、迁移和克隆性。此外,还评估了活性氧(ROS)和炎症细胞因子的水平,以及增殖、血管生成和凋亡生物标志物的表达。庆大霉素保护试验证明了粪肠球菌对癌细胞的粘附性。实时荧光定量PCR用于分析毒力基因的表达。结果显示,与对照组相比,与粪肠球菌共培养的 Cal27 细胞在细胞增殖、迁移和克隆性方面均有显著提高(粪肠球菌还下调了 p53 和 Bax 基因,同时上调了 Bcl-2)。粪肠球菌与 Cal27 细胞共培养时,毒力基因 GelE、Asa 和 Ace 过表达。本研究结果表明,感染粪肠球菌可能对口腔癌造成危害。需要针对粪大肠杆菌采取有效的抗生素策略,以预防与口腔疾病(包括癌症)相关的并发症。
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