Kitano Taku, Okumura Shintaro, Matsumoto Tomonori, Tsunoda Shigeru, Nishigori Tatsuto, Obama Kazutaka, Hara Eiji
Department of Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Department of Molecular Biology, Research Institute for Microbial Diseases, Osaka University, Suita, Japan.
Gastro Hep Adv. 2025 Mar 24;4(7):100660. doi: 10.1016/j.gastha.2025.100660. eCollection 2025.
While esophageal microbiota is known to be altered in patients with esophageal adenocarcinoma (EAC), specific bacterial species contributing to the pathogenesis remain unclear. We aimed to identify bacteria associated with the pathogenesis of EAC and to investigate their potential role.
Microbiota in EAC tissues was explored by 16S-rRNA sequencing. The impact of intratumoral bacteria on tumor microenvironment was histologically evaluated. The influence by pathological bacteria on cancer cells was examined by the treatment of OE33 cell line with cultural supernatant of bacteria.
Oral pathogenic bacteria previously reported to increase in colorectal cancer patients were detected in 7 out of 31 EAC patients and were associated with poor prognosis. Intratumoral bacterial infiltration was significantly accompanied with local neutrophil infiltration and nuclear positivity of NF-κB in cancer cells. Furthermore, the culture supernatant of applied to OE33 cells led to an upregulation of proinflammatory cytokine and chemokine genes that facilitate neutrophil migration. Notably, most of the subspecies (spp.) present in the EAC tissues were identified as spp. . The culture supernatant of spp. induced significantly more reactive oxygen species-mediated DNA damage in EAC cells than spp. , the most representative spp. of , indicating the significance of spp. rather than spp. in the pathogenesis of EAC.
Intratumoral microbiota, especially the infiltration of oral pathogenic bacteria such as , has a profound impact on the tumor microenvironment of EAC. Spp. was predominant among in the EAC tissues and induced significant DNA damage in cancer cells.
虽然已知食管腺癌(EAC)患者的食管微生物群会发生改变,但导致发病机制的特定细菌种类仍不清楚。我们旨在鉴定与EAC发病机制相关的细菌,并研究它们的潜在作用。
通过16S - rRNA测序探索EAC组织中的微生物群。从组织学上评估肿瘤内细菌对肿瘤微环境的影响。用细菌培养上清液处理OE33细胞系,检测致病细菌对癌细胞的影响。
在31例EAC患者中的7例中检测到先前报道在结直肠癌患者中增多的口腔致病细菌,且这些细菌与预后不良相关。肿瘤内细菌浸润显著伴随着局部中性粒细胞浸润以及癌细胞中NF - κB的核阳性。此外,应用于OE33细胞的培养上清液导致促炎细胞因子和趋化因子基因上调,促进中性粒细胞迁移。值得注意的是,EAC组织中存在的大多数亚种被鉴定为亚种。亚种的培养上清液在EAC细胞中诱导的活性氧介导的DNA损伤比亚种(的最具代表性亚种)显著更多,表明亚种而非亚种在EAC发病机制中具有重要意义。
肿瘤内微生物群,尤其是如等口腔致病细菌的浸润,对EAC的肿瘤微环境有深远影响。亚种在EAC组织的中占主导地位,并在癌细胞中诱导显著的DNA损伤。