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Pathophysiological Roles of Histamine Receptors in Cancer Progression: Implications and Perspectives as Potential Molecular Targets

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dc.contributor.authorNguyen, Phuong Linh-
dc.contributor.authorCho, Jungsook-
dc.date.accessioned2023-04-27T16:40:43Z-
dc.date.available2023-04-27T16:40:43Z-
dc.date.issued2021-08-
dc.identifier.issn2218-273X-
dc.identifier.issn2218-273X-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/4680-
dc.description.abstractHigh levels of histamine and histamine receptors (HRs), including H1R similar to H4R, are found in many different types of tumor cells and cells in the tumor microenvironment, suggesting their involvement in tumor progression. This review summarizes the latest evidence demonstrating the pathophysiological roles of histamine and its cognate receptors in cancer biology. We also discuss the novel therapeutic approaches of selective HR ligands and their potential prognostic values in cancer treatment. Briefly, histamine is highly implicated in cancer development, growth, and metastasis through interactions with distinct HRs. It also regulates the infiltration of immune cells into the tumor sites, exerting an immunomodulatory function. Moreover, the effects of various HR ligands, including H1R antagonists, H2R antagonists, and H4R agonists, on tumor progression in many different cancer types are described. Interestingly, the expression levels of HR subtypes may serve as prognostic biomarkers in several cancers. Taken together, HRs are promising targets for cancer treatment, and HR ligands may offer novel therapeutic potential, alone or in combination with conventional therapy. However, due to the complexity of the pathophysiological roles of histamine and HRs in cancer biology, further studies are warranted before HR ligands can be introduced into clinical settings.-
dc.language영어-
dc.language.isoENG-
dc.publisherMDPI-
dc.titlePathophysiological Roles of Histamine Receptors in Cancer Progression: Implications and Perspectives as Potential Molecular Targets-
dc.typeArticle-
dc.publisher.location스위스-
dc.identifier.doi10.3390/biom11081232-
dc.identifier.scopusid2-s2.0-85113171600-
dc.identifier.wosid000688824800001-
dc.identifier.bibliographicCitationBIOMOLECULES, v.11, no.8-
dc.citation.titleBIOMOLECULES-
dc.citation.volume11-
dc.citation.number8-
dc.type.docTypeReview-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.subject.keywordPlusTUMOR-INFILTRATING LYMPHOCYTES-
dc.subject.keywordPlusMESENCHYMAL TRANSITION PROGRESS-
dc.subject.keywordPlusNATURAL-KILLER-CELLS-
dc.subject.keywordPlusBREAST-CANCER-
dc.subject.keywordPlusCOLORECTAL-CANCER-
dc.subject.keywordPlusMAST-CELLS-
dc.subject.keywordPlusSUPPRESSOR-CELLS-
dc.subject.keywordPlusH-4 RECEPTOR-
dc.subject.keywordPlusIN-VITRO-
dc.subject.keywordPlusHISTIDINE-DECARBOXYLASE-
dc.subject.keywordAuthorhistamine-
dc.subject.keywordAuthorhistamine receptors-
dc.subject.keywordAuthorhistamine receptor ligands-
dc.subject.keywordAuthormolecular target-
dc.subject.keywordAuthortumor microenvironment-
dc.subject.keywordAuthorcancer progression-
dc.subject.keywordAuthorprognostic biomarkers-
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