BACKGROUND: Infection of hepatitis B virus (HBV) is a well-known risk factor for hepatocellular carcinoma (HCC). It is currently unknown whether gut microbiome dysbiosis in HCC tissue affects the assessment of progression and clinical outcome in patients with HBV-associated HCC. METHODS: Through a comparative analysis of 16 S gene fragments and biomarkers in tumor tissues from 40 HBV-associated HCC patients, we gained novel insights into the microbiome characteristics of HBV-associated HCC patients. RESULTS: LEfSe analysis indicated that Burkholderia cepacia (s), Microcuccus luteus (s) and Microcuccus (g) were dominant in HBV-associated HCC tissues (pâ<â0.05). 16 S rRNA-positive bacteria were not only localized in HCC cells but also overlapped with some of cells with CD68-, MPO-, α-SMA-, or CD34- positive staining in the tumor tissues. We observed that taxa abundance in HCC tissues was significantly associated with clinicopathological variables, such as tumor size, differentiation, invasion of the liver capsule, lymphovascular invasion, metastasis, pTNM, portal hypertension (PTH), Child-Turcotte-Pugh score, BCLC stage, prognosis (overall survival and progression-free survival), serum levels of α-fetoprotein, albumin, and glucose and personal habits (such as smoking and alcohol intake) of the HBV-associated HCC patients (pâ<â0.05). CONCLUSIONS: This study demonstrated that microbiome dysbiosis would have a profound effect on the progression and outcome of HBV-associated HCC. B. cepacia (s), M. luteus (s), and Microcuccus (g) would be taxon signatures in HBV-associated HCC tissues and might serve as potential targets for the treatment of patients with HBV-associated HCC. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12672-026-04654-5.
Intratumoral microbiome evaluated progression and outcome of patients with HBV-associated hepatocellular carcinoma.
阅读:2
作者:Liu Sheng-Sheng, Ye Lei, Li Xiao-Xue, Dai Qing-Qing, Gao Yi, Chen Guang-Hou, Fang Yong-Sheng, Zhao Hong-Chuan, Du Wei-Dong
| 期刊: | Discover Oncology | 影响因子: | 2.900 |
| 时间: | 2026 | 起止号: | 2026 Feb 19; 17(1):484 |
| doi: | 10.1007/s12672-026-04654-5 | ||
特别声明
1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。
2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。
3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。
4、投稿及合作请联系:info@biocloudy.com。
