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- Publisher Website: 10.1016/j.canlet.2024.217084
- Scopus: eid_2-s2.0-85196783420
- PMID: 38925362
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Article: Interplay among extracellular vesicles, cancer stemness and immune regulation in driving hepatocellular carcinoma progression
Title | Interplay among extracellular vesicles, cancer stemness and immune regulation in driving hepatocellular carcinoma progression |
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Authors | |
Keywords | Cancer stemness Extracellular vesicles Hepatocellular carcinoma Immune regulation Interplay |
Issue Date | 10-Aug-2024 |
Publisher | Elsevier |
Citation | Cancer Letters, 2024, v. 597 How to Cite? |
Abstract | The intricate interplay among extracellular vesicles, cancer stemness properties, and the immune system significantly impacts hepatocellular carcinoma (HCC) progression, treatment response, and patient prognosis. Extracellular vesicles (EVs), which are membrane-bound structures, play a pivotal role in conveying proteins, lipids, and nucleic acids between cells, thereby serving as essential mediators of intercellular communication. Since a lot of current research focuses on small extracellular vesicles (sEVs), with diameters ranging from 30 nm to 200 nm, this review emphasizes the role of sEVs in the context of interactions between HCC stemness-bearing cells and the immune cells. sEVs offer promising opportunities for the clinical application of innovative diagnostic and prognostic biomarkers in HCC. By specifically targeting sEVs, novel therapeutics aimed at cancer stemness can be developed. Ongoing investigations into the roles of sEVs in cancer stemness and immune regulation in HCC will broaden our understanding and ultimately pave the way for groundbreaking therapeutic interventions. |
Persistent Identifier | http://hdl.handle.net/10722/351826 |
ISSN | 2023 Impact Factor: 9.1 2023 SCImago Journal Rankings: 2.595 |
DC Field | Value | Language |
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dc.contributor.author | Tsui, Yu Man | - |
dc.contributor.author | Tian, Lu | - |
dc.contributor.author | Lu, Jingyi | - |
dc.contributor.author | Ma, Huanhuan | - |
dc.contributor.author | Ng, Irene Oi Lin | - |
dc.date.accessioned | 2024-12-02T00:35:04Z | - |
dc.date.available | 2024-12-02T00:35:04Z | - |
dc.date.issued | 2024-08-10 | - |
dc.identifier.citation | Cancer Letters, 2024, v. 597 | - |
dc.identifier.issn | 0304-3835 | - |
dc.identifier.uri | http://hdl.handle.net/10722/351826 | - |
dc.description.abstract | The intricate interplay among extracellular vesicles, cancer stemness properties, and the immune system significantly impacts hepatocellular carcinoma (HCC) progression, treatment response, and patient prognosis. Extracellular vesicles (EVs), which are membrane-bound structures, play a pivotal role in conveying proteins, lipids, and nucleic acids between cells, thereby serving as essential mediators of intercellular communication. Since a lot of current research focuses on small extracellular vesicles (sEVs), with diameters ranging from 30 nm to 200 nm, this review emphasizes the role of sEVs in the context of interactions between HCC stemness-bearing cells and the immune cells. sEVs offer promising opportunities for the clinical application of innovative diagnostic and prognostic biomarkers in HCC. By specifically targeting sEVs, novel therapeutics aimed at cancer stemness can be developed. Ongoing investigations into the roles of sEVs in cancer stemness and immune regulation in HCC will broaden our understanding and ultimately pave the way for groundbreaking therapeutic interventions. | - |
dc.language | eng | - |
dc.publisher | Elsevier | - |
dc.relation.ispartof | Cancer Letters | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | Cancer stemness | - |
dc.subject | Extracellular vesicles | - |
dc.subject | Hepatocellular carcinoma | - |
dc.subject | Immune regulation | - |
dc.subject | Interplay | - |
dc.title | Interplay among extracellular vesicles, cancer stemness and immune regulation in driving hepatocellular carcinoma progression | - |
dc.type | Article | - |
dc.identifier.doi | 10.1016/j.canlet.2024.217084 | - |
dc.identifier.pmid | 38925362 | - |
dc.identifier.scopus | eid_2-s2.0-85196783420 | - |
dc.identifier.volume | 597 | - |
dc.identifier.eissn | 1872-7980 | - |
dc.identifier.issnl | 0304-3835 | - |