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Article: New insights into fibrotic signaling in renal cell carcinoma

TitleNew insights into fibrotic signaling in renal cell carcinoma
Authors
Keywordscancer-associated fibroblast
mTOR
renal cell carcinoma
renal fibrosis
TGF-β
Issue Date21-Feb-2023
PublisherFrontiers Media
Citation
Frontiers in Cell and Developmental Biology, 2023, v. 11 How to Cite?
AbstractFibrotic signaling plays a pivotal role in the development and progression of solid cancers including renal cell carcinoma (RCC). Intratumoral fibrosis (ITF) and pseudo-capsule (PC) fibrosis are significantly correlated to the disease progression of renal cell carcinoma. Targeting classic fibrotic signaling processes such as TGF-β signaling and epithelial-to-mesenchymal transition (EMT) shows promising antitumor effects both preclinically and clinically. Therefore, a better understanding of the pathogenic mechanisms of fibrotic signaling in renal cell carcinoma at molecular resolution can facilitate the development of precision therapies against solid cancers. In this review, we systematically summarized the latest updates on fibrotic signaling, from clinical correlation and molecular mechanisms to its therapeutic strategies for renal cell carcinoma. Importantly, we examined the reported fibrotic signaling on the human renal cell carcinoma dataset at the transcriptome level with single-cell resolution to assess its translational potential in the clinic.
Persistent Identifierhttp://hdl.handle.net/10722/340558
ISSN
2023 Impact Factor: 4.6
2023 SCImago Journal Rankings: 1.576
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorChen, JY-
dc.contributor.authorYiu, WH-
dc.contributor.authorTang, PMK-
dc.contributor.authorTang, SCW-
dc.date.accessioned2024-03-11T10:45:30Z-
dc.date.available2024-03-11T10:45:30Z-
dc.date.issued2023-02-21-
dc.identifier.citationFrontiers in Cell and Developmental Biology, 2023, v. 11-
dc.identifier.issn2296-634X-
dc.identifier.urihttp://hdl.handle.net/10722/340558-
dc.description.abstractFibrotic signaling plays a pivotal role in the development and progression of solid cancers including renal cell carcinoma (RCC). Intratumoral fibrosis (ITF) and pseudo-capsule (PC) fibrosis are significantly correlated to the disease progression of renal cell carcinoma. Targeting classic fibrotic signaling processes such as TGF-β signaling and epithelial-to-mesenchymal transition (EMT) shows promising antitumor effects both preclinically and clinically. Therefore, a better understanding of the pathogenic mechanisms of fibrotic signaling in renal cell carcinoma at molecular resolution can facilitate the development of precision therapies against solid cancers. In this review, we systematically summarized the latest updates on fibrotic signaling, from clinical correlation and molecular mechanisms to its therapeutic strategies for renal cell carcinoma. Importantly, we examined the reported fibrotic signaling on the human renal cell carcinoma dataset at the transcriptome level with single-cell resolution to assess its translational potential in the clinic.-
dc.languageeng-
dc.publisherFrontiers Media-
dc.relation.ispartofFrontiers in Cell and Developmental Biology-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectcancer-associated fibroblast-
dc.subjectmTOR-
dc.subjectrenal cell carcinoma-
dc.subjectrenal fibrosis-
dc.subjectTGF-β-
dc.titleNew insights into fibrotic signaling in renal cell carcinoma-
dc.typeArticle-
dc.identifier.doi10.3389/fcell.2023.1056964-
dc.identifier.scopuseid_2-s2.0-85149852341-
dc.identifier.volume11-
dc.identifier.eissn2296-634X-
dc.identifier.isiWOS:000946333600001-
dc.identifier.issnl2296-634X-

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