Loading…
Tanshinone IIA Induces Apoptosis in Human Oral Cancer KB Cells through a Mitochondria-Dependent Pathway
Tanshinone IIA (Tan IIA), an active phytochemical in the dried root of Salvia miltiorrhiza Bunge, has shown an antiproliferative activity on various human cancer cell lines including nasopharyngeal carcinoma cells. However, the effects of Tan IIA on human oral cancer cells are still unknown. This st...
Saved in:
Published in: | BioMed research international 2014-01, Vol.2014 (2014), p.1-7 |
---|---|
Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c527t-1402dcb9712cd94999a0492d1b74c6074f2fdb604b88c57d152b00a4700eb4913 |
---|---|
cites | cdi_FETCH-LOGICAL-c527t-1402dcb9712cd94999a0492d1b74c6074f2fdb604b88c57d152b00a4700eb4913 |
container_end_page | 7 |
container_issue | 2014 |
container_start_page | 1 |
container_title | BioMed research international |
container_volume | 2014 |
creator | Tseng, Pao-Yu Lu, Wei-Cheng Hsieh, Ming-Ju Chien, Su-Yu Chen, Mu-Kuan |
description | Tanshinone IIA (Tan IIA), an active phytochemical in the dried root of Salvia miltiorrhiza Bunge, has shown an antiproliferative activity on various human cancer cell lines including nasopharyngeal carcinoma cells. However, the effects of Tan IIA on human oral cancer cells are still unknown. This study aimed to investigate the antiproliferative effects of Tan IIA on human oral cancer KB cells and explored the possible underlying mechanism. Treatment of KB cells with Tan IIA suppressed cell proliferation/viability and induced cell death in a dose-dependent manner through sulforhodamine B colorimetric assay. Observation of cell morphology revealed the involvement of apoptosis in the Tan IIA-induced growth inhibition on KB cells. Cell cycle analysis showed a cell cycle arrest in G2/M phase on Tan IIA-treated cells. The dissipation of mitochondrial membrane potential observed by flow cytometry and the expression of activated caspases with the cleaved poly (ADP-ribose) polymerase under immunoblotting analysis indicated that Tan IIA-induced apoptosis in KB cells was mediated through the mitochondria-dependent caspase pathway. These observations suggested that Tan IIA could be a potential anticancer agent for oral cancer. |
doi_str_mv | 10.1155/2014/540516 |
format | article |
fullrecord | <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4036409</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A427023494</galeid><sourcerecordid>A427023494</sourcerecordid><originalsourceid>FETCH-LOGICAL-c527t-1402dcb9712cd94999a0492d1b74c6074f2fdb604b88c57d152b00a4700eb4913</originalsourceid><addsrcrecordid>eNqNks1rFDEYhwdRbKk9eVYCXkQZ--ZjMpOLsK4fXazUQz2HTJLZSZlNpsmMpf-9WaauHxcNhATy8PB7w68onmJ4g3FVnRHA7KxiUGH-oDgmFLOSY4YfHu6UHhWnKV1DXg3mIPjj4ogwASBqOC62V8qn3vngLdpsVmjjzaxtQqsxjFNILiHn0fm8Ux5dRjWgtfLaRvT5HVrbYUho6mOYtz1S6Iubgu6DN9Gp8r0drTfWT-irmvpbdfekeNSpIdnT-_Ok-Pbxw9X6vLy4_LRZry5KXZF6KjEDYnQraky0EUwIoYAJYnBbM82hZh3pTMuBtU2jq9rgirQAitUAtmUC05Pi7eId53Znjc4Rcmw5RrdT8U4G5eSfL971chu-SwaUMxBZ8PJeEMPNbNMkdy7pPKvyNsxJ4orzpuKE_w9Ks5E3eI---Au9DnP0-ScyxWpB8qa_qK0arHS-Czmi3kvlipEaCGWCZer1QukYUoq2O0yHQe5LIfelkEspMv389w85sD8rkIFXC5BbYNSt-4ft2QLbjNhOHeCcP_voD8RyxNE</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1547924793</pqid></control><display><type>article</type><title>Tanshinone IIA Induces Apoptosis in Human Oral Cancer KB Cells through a Mitochondria-Dependent Pathway</title><source>Publicly Available Content Database</source><source>Wiley Open Access</source><creator>Tseng, Pao-Yu ; Lu, Wei-Cheng ; Hsieh, Ming-Ju ; Chien, Su-Yu ; Chen, Mu-Kuan</creator><contributor>Yang, Tsung-Lin</contributor><creatorcontrib>Tseng, Pao-Yu ; Lu, Wei-Cheng ; Hsieh, Ming-Ju ; Chien, Su-Yu ; Chen, Mu-Kuan ; Yang, Tsung-Lin</creatorcontrib><description>Tanshinone IIA (Tan IIA), an active phytochemical in the dried root of Salvia miltiorrhiza Bunge, has shown an antiproliferative activity on various human cancer cell lines including nasopharyngeal carcinoma cells. However, the effects of Tan IIA on human oral cancer cells are still unknown. This study aimed to investigate the antiproliferative effects of Tan IIA on human oral cancer KB cells and explored the possible underlying mechanism. Treatment of KB cells with Tan IIA suppressed cell proliferation/viability and induced cell death in a dose-dependent manner through sulforhodamine B colorimetric assay. Observation of cell morphology revealed the involvement of apoptosis in the Tan IIA-induced growth inhibition on KB cells. Cell cycle analysis showed a cell cycle arrest in G2/M phase on Tan IIA-treated cells. The dissipation of mitochondrial membrane potential observed by flow cytometry and the expression of activated caspases with the cleaved poly (ADP-ribose) polymerase under immunoblotting analysis indicated that Tan IIA-induced apoptosis in KB cells was mediated through the mitochondria-dependent caspase pathway. These observations suggested that Tan IIA could be a potential anticancer agent for oral cancer.</description><identifier>ISSN: 2314-6133</identifier><identifier>EISSN: 2314-6141</identifier><identifier>DOI: 10.1155/2014/540516</identifier><identifier>PMID: 24900970</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Puplishing Corporation</publisher><subject>Apoptosis ; Apoptosis - drug effects ; Care and treatment ; Caspases - metabolism ; Cell cycle ; Cell Death - drug effects ; Cell division ; Cell Line, Tumor ; Cell Proliferation - drug effects ; Cell Survival - drug effects ; Chinese medicine ; Cytotoxicity ; Diterpenes, Abietane - pharmacology ; Drinking water ; G2 Phase Cell Cycle Checkpoints - drug effects ; Health aspects ; Hospitals ; Humans ; KB Cells ; Medical research ; Medicine, Experimental ; Membrane Potential, Mitochondrial - drug effects ; Mitochondria ; Mitochondria - drug effects ; Mitochondria - metabolism ; Mouth cancer ; Mouth Neoplasms - drug therapy ; Mouth Neoplasms - metabolism ; Oral cancer ; Otolaryngology ; Phytochemicals ; Poly(ADP-ribose) Polymerases - metabolism ; Proteins ; Salvia miltiorrhiza ; Surgery</subject><ispartof>BioMed research international, 2014-01, Vol.2014 (2014), p.1-7</ispartof><rights>Copyright © 2014 Pao-Yu Tseng et al.</rights><rights>COPYRIGHT 2014 John Wiley & Sons, Inc.</rights><rights>Copyright © 2014 Pao-Yu Tseng et al. Pao-Yu Tseng 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.</rights><rights>Copyright © 2014 Pao-Yu Tseng et al. 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c527t-1402dcb9712cd94999a0492d1b74c6074f2fdb604b88c57d152b00a4700eb4913</citedby><cites>FETCH-LOGICAL-c527t-1402dcb9712cd94999a0492d1b74c6074f2fdb604b88c57d152b00a4700eb4913</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1547924793/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1547924793?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,25753,27924,27925,37012,37013,44590,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24900970$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Yang, Tsung-Lin</contributor><creatorcontrib>Tseng, Pao-Yu</creatorcontrib><creatorcontrib>Lu, Wei-Cheng</creatorcontrib><creatorcontrib>Hsieh, Ming-Ju</creatorcontrib><creatorcontrib>Chien, Su-Yu</creatorcontrib><creatorcontrib>Chen, Mu-Kuan</creatorcontrib><title>Tanshinone IIA Induces Apoptosis in Human Oral Cancer KB Cells through a Mitochondria-Dependent Pathway</title><title>BioMed research international</title><addtitle>Biomed Res Int</addtitle><description>Tanshinone IIA (Tan IIA), an active phytochemical in the dried root of Salvia miltiorrhiza Bunge, has shown an antiproliferative activity on various human cancer cell lines including nasopharyngeal carcinoma cells. However, the effects of Tan IIA on human oral cancer cells are still unknown. This study aimed to investigate the antiproliferative effects of Tan IIA on human oral cancer KB cells and explored the possible underlying mechanism. Treatment of KB cells with Tan IIA suppressed cell proliferation/viability and induced cell death in a dose-dependent manner through sulforhodamine B colorimetric assay. Observation of cell morphology revealed the involvement of apoptosis in the Tan IIA-induced growth inhibition on KB cells. Cell cycle analysis showed a cell cycle arrest in G2/M phase on Tan IIA-treated cells. The dissipation of mitochondrial membrane potential observed by flow cytometry and the expression of activated caspases with the cleaved poly (ADP-ribose) polymerase under immunoblotting analysis indicated that Tan IIA-induced apoptosis in KB cells was mediated through the mitochondria-dependent caspase pathway. These observations suggested that Tan IIA could be a potential anticancer agent for oral cancer.</description><subject>Apoptosis</subject><subject>Apoptosis - drug effects</subject><subject>Care and treatment</subject><subject>Caspases - metabolism</subject><subject>Cell cycle</subject><subject>Cell Death - drug effects</subject><subject>Cell division</subject><subject>Cell Line, Tumor</subject><subject>Cell Proliferation - drug effects</subject><subject>Cell Survival - drug effects</subject><subject>Chinese medicine</subject><subject>Cytotoxicity</subject><subject>Diterpenes, Abietane - pharmacology</subject><subject>Drinking water</subject><subject>G2 Phase Cell Cycle Checkpoints - drug effects</subject><subject>Health aspects</subject><subject>Hospitals</subject><subject>Humans</subject><subject>KB Cells</subject><subject>Medical research</subject><subject>Medicine, Experimental</subject><subject>Membrane Potential, Mitochondrial - drug effects</subject><subject>Mitochondria</subject><subject>Mitochondria - drug effects</subject><subject>Mitochondria - metabolism</subject><subject>Mouth cancer</subject><subject>Mouth Neoplasms - drug therapy</subject><subject>Mouth Neoplasms - metabolism</subject><subject>Oral cancer</subject><subject>Otolaryngology</subject><subject>Phytochemicals</subject><subject>Poly(ADP-ribose) Polymerases - metabolism</subject><subject>Proteins</subject><subject>Salvia miltiorrhiza</subject><subject>Surgery</subject><issn>2314-6133</issn><issn>2314-6141</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNqNks1rFDEYhwdRbKk9eVYCXkQZ--ZjMpOLsK4fXazUQz2HTJLZSZlNpsmMpf-9WaauHxcNhATy8PB7w68onmJ4g3FVnRHA7KxiUGH-oDgmFLOSY4YfHu6UHhWnKV1DXg3mIPjj4ogwASBqOC62V8qn3vngLdpsVmjjzaxtQqsxjFNILiHn0fm8Ux5dRjWgtfLaRvT5HVrbYUho6mOYtz1S6Iubgu6DN9Gp8r0drTfWT-irmvpbdfekeNSpIdnT-_Ok-Pbxw9X6vLy4_LRZry5KXZF6KjEDYnQraky0EUwIoYAJYnBbM82hZh3pTMuBtU2jq9rgirQAitUAtmUC05Pi7eId53Znjc4Rcmw5RrdT8U4G5eSfL971chu-SwaUMxBZ8PJeEMPNbNMkdy7pPKvyNsxJ4orzpuKE_w9Ks5E3eI---Au9DnP0-ScyxWpB8qa_qK0arHS-Czmi3kvlipEaCGWCZer1QukYUoq2O0yHQe5LIfelkEspMv389w85sD8rkIFXC5BbYNSt-4ft2QLbjNhOHeCcP_voD8RyxNE</recordid><startdate>20140101</startdate><enddate>20140101</enddate><creator>Tseng, Pao-Yu</creator><creator>Lu, Wei-Cheng</creator><creator>Hsieh, Ming-Ju</creator><creator>Chien, Su-Yu</creator><creator>Chen, Mu-Kuan</creator><general>Hindawi Puplishing Corporation</general><general>Hindawi Publishing Corporation</general><general>John Wiley & Sons, Inc</general><general>Hindawi Limited</general><scope>ADJCN</scope><scope>AHFXO</scope><scope>RHU</scope><scope>RHW</scope><scope>RHX</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7QO</scope><scope>7T7</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>CWDGH</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20140101</creationdate><title>Tanshinone IIA Induces Apoptosis in Human Oral Cancer KB Cells through a Mitochondria-Dependent Pathway</title><author>Tseng, Pao-Yu ; Lu, Wei-Cheng ; Hsieh, Ming-Ju ; Chien, Su-Yu ; Chen, Mu-Kuan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c527t-1402dcb9712cd94999a0492d1b74c6074f2fdb604b88c57d152b00a4700eb4913</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Apoptosis</topic><topic>Apoptosis - drug effects</topic><topic>Care and treatment</topic><topic>Caspases - metabolism</topic><topic>Cell cycle</topic><topic>Cell Death - drug effects</topic><topic>Cell division</topic><topic>Cell Line, Tumor</topic><topic>Cell Proliferation - drug effects</topic><topic>Cell Survival - drug effects</topic><topic>Chinese medicine</topic><topic>Cytotoxicity</topic><topic>Diterpenes, Abietane - pharmacology</topic><topic>Drinking water</topic><topic>G2 Phase Cell Cycle Checkpoints - drug effects</topic><topic>Health aspects</topic><topic>Hospitals</topic><topic>Humans</topic><topic>KB Cells</topic><topic>Medical research</topic><topic>Medicine, Experimental</topic><topic>Membrane Potential, Mitochondrial - drug effects</topic><topic>Mitochondria</topic><topic>Mitochondria - drug effects</topic><topic>Mitochondria - metabolism</topic><topic>Mouth cancer</topic><topic>Mouth Neoplasms - drug therapy</topic><topic>Mouth Neoplasms - metabolism</topic><topic>Oral cancer</topic><topic>Otolaryngology</topic><topic>Phytochemicals</topic><topic>Poly(ADP-ribose) Polymerases - metabolism</topic><topic>Proteins</topic><topic>Salvia miltiorrhiza</topic><topic>Surgery</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tseng, Pao-Yu</creatorcontrib><creatorcontrib>Lu, Wei-Cheng</creatorcontrib><creatorcontrib>Hsieh, Ming-Ju</creatorcontrib><creatorcontrib>Chien, Su-Yu</creatorcontrib><creatorcontrib>Chen, Mu-Kuan</creatorcontrib><collection>الدوريات العلمية والإحصائية - e-Marefa Academic and Statistical Periodicals</collection><collection>معرفة - المحتوى العربي الأكاديمي المتكامل - e-Marefa Academic Complete</collection><collection>Hindawi Publishing Complete</collection><collection>Hindawi Publishing Subscription Journals</collection><collection>Hindawi Publishing Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>Middle East & Africa Database</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>BioMed research international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tseng, Pao-Yu</au><au>Lu, Wei-Cheng</au><au>Hsieh, Ming-Ju</au><au>Chien, Su-Yu</au><au>Chen, Mu-Kuan</au><au>Yang, Tsung-Lin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tanshinone IIA Induces Apoptosis in Human Oral Cancer KB Cells through a Mitochondria-Dependent Pathway</atitle><jtitle>BioMed research international</jtitle><addtitle>Biomed Res Int</addtitle><date>2014-01-01</date><risdate>2014</risdate><volume>2014</volume><issue>2014</issue><spage>1</spage><epage>7</epage><pages>1-7</pages><issn>2314-6133</issn><eissn>2314-6141</eissn><abstract>Tanshinone IIA (Tan IIA), an active phytochemical in the dried root of Salvia miltiorrhiza Bunge, has shown an antiproliferative activity on various human cancer cell lines including nasopharyngeal carcinoma cells. However, the effects of Tan IIA on human oral cancer cells are still unknown. This study aimed to investigate the antiproliferative effects of Tan IIA on human oral cancer KB cells and explored the possible underlying mechanism. Treatment of KB cells with Tan IIA suppressed cell proliferation/viability and induced cell death in a dose-dependent manner through sulforhodamine B colorimetric assay. Observation of cell morphology revealed the involvement of apoptosis in the Tan IIA-induced growth inhibition on KB cells. Cell cycle analysis showed a cell cycle arrest in G2/M phase on Tan IIA-treated cells. The dissipation of mitochondrial membrane potential observed by flow cytometry and the expression of activated caspases with the cleaved poly (ADP-ribose) polymerase under immunoblotting analysis indicated that Tan IIA-induced apoptosis in KB cells was mediated through the mitochondria-dependent caspase pathway. These observations suggested that Tan IIA could be a potential anticancer agent for oral cancer.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Puplishing Corporation</pub><pmid>24900970</pmid><doi>10.1155/2014/540516</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2314-6133 |
ispartof | BioMed research international, 2014-01, Vol.2014 (2014), p.1-7 |
issn | 2314-6133 2314-6141 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4036409 |
source | Publicly Available Content Database; Wiley Open Access |
subjects | Apoptosis Apoptosis - drug effects Care and treatment Caspases - metabolism Cell cycle Cell Death - drug effects Cell division Cell Line, Tumor Cell Proliferation - drug effects Cell Survival - drug effects Chinese medicine Cytotoxicity Diterpenes, Abietane - pharmacology Drinking water G2 Phase Cell Cycle Checkpoints - drug effects Health aspects Hospitals Humans KB Cells Medical research Medicine, Experimental Membrane Potential, Mitochondrial - drug effects Mitochondria Mitochondria - drug effects Mitochondria - metabolism Mouth cancer Mouth Neoplasms - drug therapy Mouth Neoplasms - metabolism Oral cancer Otolaryngology Phytochemicals Poly(ADP-ribose) Polymerases - metabolism Proteins Salvia miltiorrhiza Surgery |
title | Tanshinone IIA Induces Apoptosis in Human Oral Cancer KB Cells through a Mitochondria-Dependent Pathway |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T15%3A32%3A05IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Tanshinone%20IIA%20Induces%20Apoptosis%20in%20Human%20Oral%20Cancer%20KB%20Cells%20through%20a%20Mitochondria-Dependent%20Pathway&rft.jtitle=BioMed%20research%20international&rft.au=Tseng,%20Pao-Yu&rft.date=2014-01-01&rft.volume=2014&rft.issue=2014&rft.spage=1&rft.epage=7&rft.pages=1-7&rft.issn=2314-6133&rft.eissn=2314-6141&rft_id=info:doi/10.1155/2014/540516&rft_dat=%3Cgale_pubme%3EA427023494%3C/gale_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c527t-1402dcb9712cd94999a0492d1b74c6074f2fdb604b88c57d152b00a4700eb4913%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1547924793&rft_id=info:pmid/24900970&rft_galeid=A427023494&rfr_iscdi=true |