外体
金黄色葡萄球菌
肿瘤微环境
癌变
肺癌
生物
生物膜
炎症
微生物学
微泡
肿瘤进展
癌症研究
串扰
失调
癌症
免疫学
细菌
肠道菌群
医学
病理
肿瘤细胞
基因
小RNA
物理
光学
生物化学
遗传学
作者
Jipeng Jiang,Jie Mei,Shasha Jiang,Jian Zhang,Liuxiang Wang,Jing Yuan,Shaoqiong Yi,Yongfu Ma,Yang Liu
出处
期刊:Nano Today
[Elsevier BV]
日期:2022-03-17
卷期号:44: 101451-101451
被引量:6
标识
DOI:10.1016/j.nantod.2022.101451
摘要
Tumor microenvironment (TME) is a dynamic niche for tumorigenesis and progression. Emerging evidence has shed light on the unusual role of commensal microbiota in the TME across various tumors. Microbiota can have long-time exist in the TME or even in tumor cells without uncontrolled proliferation and fatal infection to tumor cells, and it can interact with tumor cells when they coexist. Specific microbiota can contribute to carcinogenesis by inducing tumor-associated inflammation, producing immunosuppressive factors, and releasing detrimental metabolites. But less is known about how the tumor cells can exert effects and modulate the commensal microbiota. In this study, we found that the tumor tissues of patients with lung adenocarcinoma were enriched with Staphylococcus aureus (S. aureus) relative to the adjacent tissues, and the lung cancer-derived exosome-like nanoparticles (ELNs) can be internalized by S. aureus, the treatment of lung cancer-derived ELNs altered the bacterial morphology, reduced the adhesion ability, biofilm formation and the virulence of S. aureus, the activation of ArlS-ArlR two-component system may be one of the potential mechanisms under the above phenomenon. It is a novel revelation of the crosstalk between tumor cells and the commensal microbiota.
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