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- Publisher Website: 10.1002/pmic.200700829
- Scopus: eid_2-s2.0-49749104260
- PMID: 18615425
- WOS: WOS:000258503400012
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Article: Proteomic and transcriptomic study on the action of a cytotoxic saponin (Polyphyllin D): Induction of endoplasmic reticulum stress and mitochondria-mediated apoptotic pathways
Title | Proteomic and transcriptomic study on the action of a cytotoxic saponin (Polyphyllin D): Induction of endoplasmic reticulum stress and mitochondria-mediated apoptotic pathways |
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Authors | |
Keywords | Apoptosis Lung cancer Proteomics Saponin Transcriptomics |
Issue Date | 2008 |
Publisher | Wiley - V C H Verlag GmbH & Co KGaA. The Journal's web site is located at http://www.wiley-vch.de/home/proteomics |
Citation | Proteomics, 2008, v. 8 n. 15, p. 3105-3117 How to Cite? |
Abstract | Polyphyllin D (PD) is a potent cytotoxic saponin found in Paris polyphylla. In the present study, bioinformatic, proteomic and transcriptomic analyses were performed to study the mechanisms of action of PD on human nonsmall cell lung cancer (NSCLC) cell line (NCI-H460). Using a gene expression-based bioinformatic tool (connectivity map), PD was identified as a potential ER stress inducer. Our proteomic and transcriptomic analyses revealed that PD treatment led to upregulation of typical ER stress-related proteins/genes including glucose-regulated protein 78 (BiP/GRP78) and protein disulfide isomerase (PDI). In particular, elevated expression of C/EBP homologous transcription factor (chop) and activation of caspase-4 occurred at early time point (8 h) of PD treatment, signifying an initial ER stress-mediated apoptosis. Induction of tumor suppressor p53, disruption of mitochondrial membrane, activation of caspase-9 and caspase-3 were detected upon prolonged PD treatment. Collectively, these data revealed that PD induced the cytotoxic effect through a mechanism initiated by ER stress followed by mitochondrial apoptotic pathway. The ability of activating two major pathways of apoptosis makes PD an attractive drug lead for anticancer therapeutics. © 2008 Wiley-VCH Verlag GmbH & Co. KGaA. |
Persistent Identifier | http://hdl.handle.net/10722/168319 |
ISSN | 2023 Impact Factor: 3.4 2023 SCImago Journal Rankings: 1.011 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Siu, FM | en_US |
dc.contributor.author | Ma, DL | en_US |
dc.contributor.author | Cheung, YW | en_US |
dc.contributor.author | Lok, CN | en_US |
dc.contributor.author | Yan, K | en_US |
dc.contributor.author | Yang, Z | en_US |
dc.contributor.author | Yang, M | en_US |
dc.contributor.author | Xu, S | en_US |
dc.contributor.author | Ko, BCB | en_US |
dc.contributor.author | He, QY | en_US |
dc.contributor.author | Che, CM | en_US |
dc.date.accessioned | 2012-10-08T03:17:29Z | - |
dc.date.available | 2012-10-08T03:17:29Z | - |
dc.date.issued | 2008 | en_US |
dc.identifier.citation | Proteomics, 2008, v. 8 n. 15, p. 3105-3117 | en_US |
dc.identifier.issn | 1615-9853 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/168319 | - |
dc.description.abstract | Polyphyllin D (PD) is a potent cytotoxic saponin found in Paris polyphylla. In the present study, bioinformatic, proteomic and transcriptomic analyses were performed to study the mechanisms of action of PD on human nonsmall cell lung cancer (NSCLC) cell line (NCI-H460). Using a gene expression-based bioinformatic tool (connectivity map), PD was identified as a potential ER stress inducer. Our proteomic and transcriptomic analyses revealed that PD treatment led to upregulation of typical ER stress-related proteins/genes including glucose-regulated protein 78 (BiP/GRP78) and protein disulfide isomerase (PDI). In particular, elevated expression of C/EBP homologous transcription factor (chop) and activation of caspase-4 occurred at early time point (8 h) of PD treatment, signifying an initial ER stress-mediated apoptosis. Induction of tumor suppressor p53, disruption of mitochondrial membrane, activation of caspase-9 and caspase-3 were detected upon prolonged PD treatment. Collectively, these data revealed that PD induced the cytotoxic effect through a mechanism initiated by ER stress followed by mitochondrial apoptotic pathway. The ability of activating two major pathways of apoptosis makes PD an attractive drug lead for anticancer therapeutics. © 2008 Wiley-VCH Verlag GmbH & Co. KGaA. | en_US |
dc.language | eng | en_US |
dc.publisher | Wiley - V C H Verlag GmbH & Co KGaA. The Journal's web site is located at http://www.wiley-vch.de/home/proteomics | en_US |
dc.relation.ispartof | Proteomics | en_US |
dc.subject | Apoptosis | - |
dc.subject | Lung cancer | - |
dc.subject | Proteomics | - |
dc.subject | Saponin | - |
dc.subject | Transcriptomics | - |
dc.subject.mesh | Apoptosis - Drug Effects | en_US |
dc.subject.mesh | Carcinoma, Non-Small-Cell Lung - Genetics - Metabolism - Pathology | en_US |
dc.subject.mesh | Cell Line, Tumor | en_US |
dc.subject.mesh | Diosgenin - Analogs & Derivatives - Pharmacology | en_US |
dc.subject.mesh | Endoplasmic Reticulum - Metabolism | en_US |
dc.subject.mesh | Gene Expression Profiling - Methods | en_US |
dc.subject.mesh | Gene Expression Regulation, Neoplastic - Drug Effects | en_US |
dc.subject.mesh | Heat-Shock Proteins - Genetics - Metabolism | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Lung Neoplasms - Genetics - Metabolism - Pathology | en_US |
dc.subject.mesh | Mitochondria - Metabolism | en_US |
dc.subject.mesh | Molecular Chaperones - Genetics - Metabolism | en_US |
dc.subject.mesh | Proteomics - Methods | en_US |
dc.subject.mesh | Signal Transduction - Drug Effects | en_US |
dc.subject.mesh | Transcription Factor Chop - Genetics - Metabolism | en_US |
dc.subject.mesh | Tumor Suppressor Protein P53 - Genetics - Metabolism | en_US |
dc.title | Proteomic and transcriptomic study on the action of a cytotoxic saponin (Polyphyllin D): Induction of endoplasmic reticulum stress and mitochondria-mediated apoptotic pathways | en_US |
dc.type | Article | en_US |
dc.identifier.email | Siu, FM:fmsiu@hku.hk | en_US |
dc.identifier.email | Ma, DL:edmondma@hku.hk | en_US |
dc.identifier.email | Lok, CN:cnlok@hku.hk | en_US |
dc.identifier.email | Che, CM:cmche@hku.hk | en_US |
dc.identifier.authority | Siu, FM=rp00776 | en_US |
dc.identifier.authority | Ma, DL=rp00760 | en_US |
dc.identifier.authority | Lok, CN=rp00752 | en_US |
dc.identifier.authority | Che, CM=rp00670 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1002/pmic.200700829 | en_US |
dc.identifier.pmid | 18615425 | - |
dc.identifier.scopus | eid_2-s2.0-49749104260 | en_US |
dc.identifier.hkuros | 147777 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-49749104260&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 8 | en_US |
dc.identifier.issue | 15 | en_US |
dc.identifier.spage | 3105 | en_US |
dc.identifier.epage | 3117 | en_US |
dc.identifier.eissn | 1615-9861 | - |
dc.identifier.isi | WOS:000258503400012 | - |
dc.publisher.place | Germany | en_US |
dc.identifier.scopusauthorid | Siu, FM=6701518489 | en_US |
dc.identifier.scopusauthorid | Ma, DL=7402075538 | en_US |
dc.identifier.scopusauthorid | Cheung, YW=24586913200 | en_US |
dc.identifier.scopusauthorid | Lok, CN=7006410829 | en_US |
dc.identifier.scopusauthorid | Yan, K=35340293700 | en_US |
dc.identifier.scopusauthorid | Yang, Z=13205034800 | en_US |
dc.identifier.scopusauthorid | Yang, M=7404925734 | en_US |
dc.identifier.scopusauthorid | Xu, S=24475645200 | en_US |
dc.identifier.scopusauthorid | Ko, BCB=7102833927 | en_US |
dc.identifier.scopusauthorid | He, QY=34770287900 | en_US |
dc.identifier.scopusauthorid | Che, CM=7102442791 | en_US |
dc.identifier.issnl | 1615-9853 | - |