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Article: The Role of Gut Microbial β-Glucuronidase in Estrogen Reactivation and Breast Cancer

TitleThe Role of Gut Microbial β-Glucuronidase in Estrogen Reactivation and Breast Cancer
Authors
Keywordsgut microbial β-glucuronidase
estrogen reactivation
breast cancer
host-microbe interaction
gut microbiota
Issue Date2021
PublisherFrontiers Research Foundation. The Journal's web site is located at https://www.frontiersin.org/journals/cell-and-developmental-biology
Citation
Frontiers in Cell and Developmental Biology, 2021, v. 9, p. article no. 631552 How to Cite?
AbstractOver the past decade, the gut microbiota has received considerable attention for its interactions with the host. Microbial β-glucuronidase generated by this community has hence aroused concern for its biotransformation activity to a wide range of exogenous (foreign) and endogenous compounds. Lately, the role of gut microbial β-glucuronidase in the pathogenesis of breast cancer has been proposed for its estrogen reactivation activity. This is plausible considering that estrogen glucuronides are the primary products of estrogens’ hepatic phase II metabolism and are subject to β-glucuronidase-catalyzed hydrolysis in the gut via bile excretion. However, research in this field is still at its very preliminary stage. This review outlines the biology of microbial β-glucuronidase in the gastrointestinal tract and elaborates on the clues to the existence of microbial β-glucuronidase–estrogen metabolism–breast cancer axis. The research gaps in this field will be discussed and possible strategies to address these challenges are suggested.
Persistent Identifierhttp://hdl.handle.net/10722/308488
ISSN
2023 Impact Factor: 4.6
2023 SCImago Journal Rankings: 1.576
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorSUI, Y-
dc.contributor.authorWu, J-
dc.contributor.authorChen, J-
dc.date.accessioned2021-12-01T07:54:01Z-
dc.date.available2021-12-01T07:54:01Z-
dc.date.issued2021-
dc.identifier.citationFrontiers in Cell and Developmental Biology, 2021, v. 9, p. article no. 631552-
dc.identifier.issn2296-634X-
dc.identifier.urihttp://hdl.handle.net/10722/308488-
dc.description.abstractOver the past decade, the gut microbiota has received considerable attention for its interactions with the host. Microbial β-glucuronidase generated by this community has hence aroused concern for its biotransformation activity to a wide range of exogenous (foreign) and endogenous compounds. Lately, the role of gut microbial β-glucuronidase in the pathogenesis of breast cancer has been proposed for its estrogen reactivation activity. This is plausible considering that estrogen glucuronides are the primary products of estrogens’ hepatic phase II metabolism and are subject to β-glucuronidase-catalyzed hydrolysis in the gut via bile excretion. However, research in this field is still at its very preliminary stage. This review outlines the biology of microbial β-glucuronidase in the gastrointestinal tract and elaborates on the clues to the existence of microbial β-glucuronidase–estrogen metabolism–breast cancer axis. The research gaps in this field will be discussed and possible strategies to address these challenges are suggested.-
dc.languageeng-
dc.publisherFrontiers Research Foundation. The Journal's web site is located at https://www.frontiersin.org/journals/cell-and-developmental-biology-
dc.relation.ispartofFrontiers in Cell and Developmental Biology-
dc.rightsThis Document is Protected by copyright and was first published by Frontiers. All rights reserved. It is reproduced with permission.-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectgut microbial β-glucuronidase-
dc.subjectestrogen reactivation-
dc.subjectbreast cancer-
dc.subjecthost-microbe interaction-
dc.subjectgut microbiota-
dc.titleThe Role of Gut Microbial β-Glucuronidase in Estrogen Reactivation and Breast Cancer-
dc.typeArticle-
dc.identifier.emailChen, J: abchen@hkucc.hku.hk-
dc.identifier.authorityChen, J=rp01316-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.3389/fcell.2021.631552-
dc.identifier.pmid34458248-
dc.identifier.pmcidPMC8388929-
dc.identifier.scopuseid_2-s2.0-85113896753-
dc.identifier.hkuros330440-
dc.identifier.volume9-
dc.identifier.spagearticle no. 631552-
dc.identifier.epagearticle no. 631552-
dc.identifier.isiWOS:000685126700008-
dc.publisher.placeSwitzerland-

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