Miyabe Katsuyuki, Chandrasekhara Vinay, Wongjarupong Nicha, Chen Jun, Yang Lu, Johnson Stephen, Chia Nicholas, Walther-Antonio Marina, Yao Janet Z, Harrington Sean C, Nordyke Cynthia K, Eaton John E, Gossard Andrea A, Oli Sharad, Ali Hamdi A, Lavu Sravanthi, Giama Nasra H, Hassan Fatima A, Ali Hawa M, Enders Felicity T, Ilyas Sumera I, Gores Gregory J, Topazian Mark D, Kashyap Purna C, Roberts Lewis R
Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN 55905, USA.
Department of Gastroenterology, Japanese Red Cross Aichi Medical Center Nagoya Daini Hospital, Nagoya 466-8650, Japan.
Cancers (Basel). 2022 Apr 24;14(9):2120. doi: 10.3390/cancers14092120.
Primary sclerosing cholangitis (PSC) is a major risk factor for cholangiocarcinoma (CCA). We investigated biliary and fecal microbiota to determine whether specific microbes in the bile or stool are associated with PSC or CCA.
Bile was obtained from 32 patients with PSC, 23 with CCA with PSC, 26 with CCA without PSC, and 17 controls. Over 90% of bile samples were from patients with perihilar CCA. Stool was obtained from 31 patients with PSC (11 were matched to bile), 16 with CCA with PSC (10 matched to bile), and 11 with CCA without PSC (6 matched to bile). Microbiota composition was assessed using 16SrRNA-marker-based sequencing and was compared between groups.
Bile has a unique microbiota distinguished from negative DNA controls and stool. Increased species richness and abundance of Fusobacteria correlated with duration of PSC and characterized the biliary microbiota in CCA. Stool microbiota composition showed no significant differences between groups.
We identified a unique microbial signature in the bile of patients with increased duration of PSC or with CCA, suggesting a role for microbiota-driven inflammation in the pathogenesis and or progression to perihilar CCA. Further studies are needed to test this hypothesis.
原发性硬化性胆管炎(PSC)是胆管癌(CCA)的主要危险因素。我们研究了胆汁和粪便微生物群,以确定胆汁或粪便中的特定微生物是否与PSC或CCA相关。
从32例PSC患者、23例合并PSC的CCA患者、26例不合并PSC的CCA患者和17例对照者中获取胆汁。超过90%的胆汁样本来自肝门周围CCA患者。从31例PSC患者(其中11例与胆汁样本匹配)、16例合并PSC的CCA患者(其中10例与胆汁样本匹配)和11例不合并PSC的CCA患者(其中6例与胆汁样本匹配)中获取粪便。使用基于16SrRNA标记的测序评估微生物群组成,并在组间进行比较。
胆汁具有独特的微生物群,与阴性DNA对照和粪便不同。梭杆菌属物种丰富度和丰度的增加与PSC的病程相关,并可作为CCA胆汁微生物群的特征。各组粪便微生物群组成无显著差异。
我们在PSC病程延长或患有CCA的患者胆汁中鉴定出一种独特的微生物特征,提示微生物群驱动的炎症在肝门周围CCA的发病机制和/或进展中起作用。需要进一步研究来验证这一假设。