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- Publisher Website: 10.3389/fphar.2021.650039
- Scopus: eid_2-s2.0-85105129629
- PMID: 33953683
- WOS: WOS:000646174700001
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Article: Human Pluripotent Stem Cells for Modeling of Anticancer Therapy-Induced Cardiotoxicity and Cardioprotective Drug Discovery
Title | Human Pluripotent Stem Cells for Modeling of Anticancer Therapy-Induced Cardiotoxicity and Cardioprotective Drug Discovery |
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Authors | |
Keywords | anticancer therapy cardiotoxicity human induced pluripotent cells cardiomyocytes pharmacogenomics |
Issue Date | 2021 |
Publisher | Frontiers Research Foundation. The Journal's web site is located at http://www.frontiersin.org/pharmacology |
Citation | Frontiers in Pharmacology, 2021, v. 12, p. article no. 650039 How to Cite? |
Abstract | Anticancer chemotherapies have been shown to produce severe side effects, with cardiotoxicity from anthracycline being the most notable. Identifying risk factors for anticancer therapy-induced cardiotoxicity in cancer patients as well as understanding its underlying mechanism is essential to improving clinical outcomes of chemotherapy treatment regimens. Moreover, cardioprotective agents against anticancer therapy-induced cardiotoxicity are scarce. Human induced pluripotent stem cell technology offers an attractive platform for validation of potential single nucleotide polymorphism with increased risk for cardiotoxicity. Successful validation of risk factors and mechanism of cardiotoxicity would aid the development of such platform for novel drug discovery and facilitate the practice of personalized medicine. |
Persistent Identifier | http://hdl.handle.net/10722/302362 |
ISSN | 2023 Impact Factor: 4.4 2023 SCImago Journal Rankings: 1.066 |
PubMed Central ID | |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Keung, W | - |
dc.contributor.author | Cheung, YF | - |
dc.date.accessioned | 2021-09-06T03:31:12Z | - |
dc.date.available | 2021-09-06T03:31:12Z | - |
dc.date.issued | 2021 | - |
dc.identifier.citation | Frontiers in Pharmacology, 2021, v. 12, p. article no. 650039 | - |
dc.identifier.issn | 1663-9812 | - |
dc.identifier.uri | http://hdl.handle.net/10722/302362 | - |
dc.description.abstract | Anticancer chemotherapies have been shown to produce severe side effects, with cardiotoxicity from anthracycline being the most notable. Identifying risk factors for anticancer therapy-induced cardiotoxicity in cancer patients as well as understanding its underlying mechanism is essential to improving clinical outcomes of chemotherapy treatment regimens. Moreover, cardioprotective agents against anticancer therapy-induced cardiotoxicity are scarce. Human induced pluripotent stem cell technology offers an attractive platform for validation of potential single nucleotide polymorphism with increased risk for cardiotoxicity. Successful validation of risk factors and mechanism of cardiotoxicity would aid the development of such platform for novel drug discovery and facilitate the practice of personalized medicine. | - |
dc.language | eng | - |
dc.publisher | Frontiers Research Foundation. The Journal's web site is located at http://www.frontiersin.org/pharmacology | - |
dc.relation.ispartof | Frontiers in Pharmacology | - |
dc.rights | This Document is Protected by copyright and was first published by Frontiers. All rights reserved. It is reproduced with permission. | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | anticancer therapy | - |
dc.subject | cardiotoxicity | - |
dc.subject | human induced pluripotent cells | - |
dc.subject | cardiomyocytes | - |
dc.subject | pharmacogenomics | - |
dc.title | Human Pluripotent Stem Cells for Modeling of Anticancer Therapy-Induced Cardiotoxicity and Cardioprotective Drug Discovery | - |
dc.type | Article | - |
dc.identifier.email | Keung, W: wkeung@hku.hk | - |
dc.identifier.email | Cheung, YF: xfcheung@hku.hk | - |
dc.identifier.authority | Keung, W=rp01887 | - |
dc.identifier.authority | Cheung, YF=rp00382 | - |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.3389/fphar.2021.650039 | - |
dc.identifier.pmid | 33953683 | - |
dc.identifier.pmcid | PMC8090862 | - |
dc.identifier.scopus | eid_2-s2.0-85105129629 | - |
dc.identifier.hkuros | 324839 | - |
dc.identifier.volume | 12 | - |
dc.identifier.spage | article no. 650039 | - |
dc.identifier.epage | article no. 650039 | - |
dc.identifier.isi | WOS:000646174700001 | - |
dc.publisher.place | Switzerland | - |