Contributions of the Microbiome-Derived Metabolome for Risk Assessment and Prognostication of Pancreatic Cancer

代谢组 微生物群 生物标志物 胰腺癌 失调 生物 胰腺 代谢物 癌症 代谢组学 克拉斯 癌症研究 生物信息学 医学 结直肠癌 内分泌学 遗传学
作者
Ricardo A. León-Letelier,Rongzhang Dou,Jody V. Vykoukal,Michele Yip-Schneider,Anirban Maitra,Ehsan Irajizad,Ranran Wu,Jennifer B. Dennison,Kim-An Do,Jianjun Zhang,C. Max Schmidt,Samir Hanash,Johannes F. Fahrmann
出处
期刊:Clinical Chemistry [American Association for Clinical Chemistry]
卷期号:70 (1): 102-115 被引量:4
标识
DOI:10.1093/clinchem/hvad186
摘要

Abstract Background Increasing evidence implicates microbiome involvement in the development and progression of pancreatic ductal adenocarcinoma (PDAC). Studies suggest that reflux of gut or oral microbiota can lead to colonization in the pancreas, resulting in dysbiosis that culminates in release of microbial toxins and metabolites that potentiate an inflammatory response and increase susceptibility to PDAC. Moreover, microbe-derived metabolites can exert direct effector functions on precursors and cancer cells, as well as other cell types, to either promote or attenuate tumor development and modulate treatment response. Content The occurrence of microbial metabolites in biofluids thereby enables risk assessment and prognostication of PDAC, as well as having potential for design of interception strategies. In this review, we first highlight the relevance of the microbiome for progression of precancerous lesions in the pancreas and, using liquid chromatography–mass spectrometry, provide supporting evidence that microbe-derived metabolites manifest in pancreatic cystic fluid and are associated with malignant progression of intraductal papillary mucinous neoplasm(s). We secondly summarize the biomarker potential of microbe-derived metabolite signatures for (a) identifying individuals at high risk of developing or harboring PDAC and (b) predicting response to treatment and disease outcomes. Summary The microbiome-derived metabolome holds considerable promise for risk assessment and prognostication of PDAC.

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