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dc.contributor.authorChen, Kuan-Chung
dc.contributor.authorChen, Hsin-Yi
dc.contributor.authorChen, Calvin Yu-Chian
dc.date.accessioned2015-03-19T20:22:00Z
dc.date.available2015-03-19T20:22:00Z
dc.date.issued2014-04
dc.date.submitted2014-01
dc.identifier.issn1741-427X
dc.identifier.issn1741-4288
dc.identifier.otherArticle ID 436863
dc.identifier.urihttp://hdl.handle.net/1721.1/96094
dc.description.abstractProtein phosphatase 2A (PP2A) is an important phosphatase which regulates various cellular processes, such as protein synthesis, cell growth, cellular signaling, apoptosis, metabolism, and stress responses. It is a holoenzyme composed of the structural A and catalytic C subunits and a regulatory B subunit. As an environmental toxin, okadaic acid, is a tumor promoter and binds to PP2A catalytic C subunit and the cancer-associated mutations in PP2A structural A subunit in human tumor tissue; PP2A may have tumor-suppressing function. It is a potential drug target in the treatment of cancer. In this study, we screen the TCM compounds in TCM Database@Taiwan to investigate the potent lead compounds as PP2A agent. The results of docking simulation are optimized under dynamic conditions by MD simulations after virtual screening to validate the stability of H-bonds between PP2A-α protein and each ligand. The top TCM candidates, trichosanatine and squamosamide, have potential binding affinities and interactions with key residues Arg89 and Arg214 in the docking simulation. In addition, these interactions were stable under dynamic conditions. Hence, we propose the TCM compounds, trichosanatine and squamosamide, as potential candidates as lead compounds for further study in drug development process with the PP2A-α protein.en_US
dc.description.sponsorshipNational Science Council of Taiwan (NSC102-2325-B039-001)en_US
dc.description.sponsorshipNational Science Council of Taiwan (NSC102-2221-E-468-027-)en_US
dc.description.sponsorshipAsia University (Taiwan) (Asia101-CMU- 2, 102-Asia-07)en_US
dc.description.sponsorshipChina Medical University (Hospital, DMR-103-058)en_US
dc.description.sponsorshipChina Medical University (Hospital, DMR-103-001)en_US
dc.description.sponsorshipChina Medical University (Hospital, DMR-103-096)en_US
dc.description.sponsorshipTaiwan Department of Health. Clinical Trial and Research Center of Excellenceen_US
dc.description.sponsorshipTaiwan Department of Health. Clinical Trial and Research Center of Excellence (DOH102-TD-B-111-004)en_US
dc.description.sponsorshipTaiwan Department of Health. Clinical Trial and Research Center of Excellence (MOHW103-TD-B-111-03)en_US
dc.publisherHindawi Publishing Corporationen_US
dc.relation.isversionofhttp://dx.doi.org/10.1155/2014/436863en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by/2.0en_US
dc.sourceHindawi Publishing Corporationen_US
dc.titlePotential Protein Phosphatase 2A Agents from Traditional Chinese Medicine against Canceren_US
dc.typeArticleen_US
dc.identifier.citationChen, Kuan-Chung, Hsin-Yi Chen, and Calvin Yu-Chian Chen. "Potential Protein Phosphatase 2A Agents from Traditional Chinese Medicine against Cancer." Evidence-Based Complementary and Alternative Medicine Volume 2014 (2014), Article ID 436863, 10 p.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Computational and Systems Biology Programen_US
dc.contributor.mitauthorChen, Calvin Yu-Chianen_US
dc.relation.journalEvidence-Based Complementary and Alternative Medicineen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2015-03-19T11:33:30Z
dc.language.rfc3066en
dc.rights.holderCopyright © 2014 Kuan-Chung Chen et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
dspace.orderedauthorsChen, Kuan-Chung; Chen, Hsin-Yi; Chen, Calvin Yu-Chianen_US
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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