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- Publisher Website: 10.3389/fcell.2023.1056964
- Scopus: eid_2-s2.0-85149852341
- WOS: WOS:000946333600001
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Article: New insights into fibrotic signaling in renal cell carcinoma
Title | New insights into fibrotic signaling in renal cell carcinoma |
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Authors | |
Keywords | cancer-associated fibroblast mTOR renal cell carcinoma renal fibrosis TGF-β |
Issue Date | 21-Feb-2023 |
Publisher | Frontiers Media |
Citation | Frontiers in Cell and Developmental Biology, 2023, v. 11 How to Cite? |
Abstract | Fibrotic 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 Identifier | http://hdl.handle.net/10722/340558 |
ISSN | 2023 Impact Factor: 4.6 2023 SCImago Journal Rankings: 1.576 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Chen, JY | - |
dc.contributor.author | Yiu, WH | - |
dc.contributor.author | Tang, PMK | - |
dc.contributor.author | Tang, SCW | - |
dc.date.accessioned | 2024-03-11T10:45:30Z | - |
dc.date.available | 2024-03-11T10:45:30Z | - |
dc.date.issued | 2023-02-21 | - |
dc.identifier.citation | Frontiers in Cell and Developmental Biology, 2023, v. 11 | - |
dc.identifier.issn | 2296-634X | - |
dc.identifier.uri | http://hdl.handle.net/10722/340558 | - |
dc.description.abstract | Fibrotic 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.language | eng | - |
dc.publisher | Frontiers Media | - |
dc.relation.ispartof | Frontiers in Cell and Developmental Biology | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | cancer-associated fibroblast | - |
dc.subject | mTOR | - |
dc.subject | renal cell carcinoma | - |
dc.subject | renal fibrosis | - |
dc.subject | TGF-β | - |
dc.title | New insights into fibrotic signaling in renal cell carcinoma | - |
dc.type | Article | - |
dc.identifier.doi | 10.3389/fcell.2023.1056964 | - |
dc.identifier.scopus | eid_2-s2.0-85149852341 | - |
dc.identifier.volume | 11 | - |
dc.identifier.eissn | 2296-634X | - |
dc.identifier.isi | WOS:000946333600001 | - |
dc.identifier.issnl | 2296-634X | - |