Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/115815
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dc.contributorDepartment of Applied Biology and Chemical Technology-
dc.creatorYang, H-
dc.creatorLei, MML-
dc.creatorXie, L-
dc.creatorShou, Y-
dc.creatorLee, TKW-
dc.date.accessioned2025-11-04T03:15:51Z-
dc.date.available2025-11-04T03:15:51Z-
dc.identifier.issn2287-2728-
dc.identifier.urihttp://hdl.handle.net/10397/115815-
dc.language.isoenen_US
dc.publisherKorean Association for the Study of the Liveren_US
dc.rightsCopyright © 2025 by Korean Association for the Study of the Liveren_US
dc.rightsThis is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.en_US
dc.rightsThe following publication Yang, H., Lei, M. M. L., Xie, L., Shou, Y., & Lee, T. K. W. (2025). Deciphering adenosine signaling in hepatocellular carcinoma: Pathways, prognostic models, and therapeutic implications. Clin Mol Hepatol, 31(3), 706–729 is available at https://doi.org/10.3350/cmh.2024.1068.en_US
dc.subjectAdenosineen_US
dc.subjectHepatocellular carcinomaen_US
dc.subjectPrognosisen_US
dc.subjectReceptors, purinergicen_US
dc.subjectSignal transductionen_US
dc.titleDeciphering adenosine signaling in hepatocellular carcinoma : pathways, prognostic models, and therapeutic implicationsen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage706-
dc.identifier.epage729-
dc.identifier.volume31-
dc.identifier.issue3-
dc.identifier.doi10.3350/cmh.2024.1068-
dcterms.abstractHepatocellular carcinoma (HCC) is a highly lethal cancer due to its aggressive nature and poor prognosis. Adenosine, a key metabolic regulator in the tumor microenvironment (TME), plays a crucial role in cancer progression. In this review, we first described adenosine triphosphate adenosine metabolism in the TME and summarized its effects on tumor growth, immune suppression, angiogenesis, and metastasis in HCC. Given the limited number of clinical studies on adenosine signaling in HCC, we conducted LASSO-Cox analysis using the TCGA-LIHC cohort to develop a prognostic risk model composed of eight adenosine signaling-related genes. This model stratified the patients into low- and high-risk groups, with Kaplan-Meier survival analysis revealing poorer overall survival in the high-risk group. Additionally, differential gene expression analysis between the two groups identified 24 enriched signaling pathways for further investigation. Immune infiltration and single cell RNA-seq analyses revealed a correlation between adenosine and immunosuppressive activity in the TME, with a particularly strong association observed in macrophages, dendritic cells, and monocytes. Finally, we provided an overview of the advancements of antagonists that target adenosine receptors’ progress in both preclinical research and clinical trials. In conclusion, this review aims to deepen our understanding of the biological role of adenosine and highlights emerging therapeutic strategies that may improve treatment outcomes for HCC.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationClinical and molecular hepatology, July 2025, v. 31, no. 3, p. 706-729-
dcterms.isPartOfClinical and molecular hepatology-
dcterms.issued2025-07-
dc.identifier.scopus2-s2.0-105010712297-
dc.identifier.eissn2287-285X-
dc.description.validate202511 bcch-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOSen_US
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThis work was supported by RGC General Research Fund (15102722) and Research Impact Fund (R7022-20 and R5008-22F).en_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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