Extracellular polymeric substance from Aphanizomenon flos-aquae induces apoptosis via the mitochondrial pathway in A431 human epidermoid carcinoma cells
Extracellular polymeric substance (EPS) is a substance secreted during algal growth, which has been found to have numerous health-promoting effects. In the present study, A431 human epidermoid carcinoma cells were selected as target cells and cultivated in vitro as an experimental model to investiga...
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description | Extracellular polymeric substance (EPS) is a substance secreted during algal growth, which has been found to have numerous health-promoting effects. In the present study, A431 human epidermoid carcinoma cells were selected as target cells and cultivated in vitro as an experimental model to investigate the anti-cancer effect of extracellular polymeric substances from Aphanizomenon flos-aquae (EPS-A) and the possible underlying mechanism. Apoptosis- and cell cycle-associated molecules as well as the mitochondrial membrane potential of the cells were quantified using flow cytometry (FCM). FCM showed that EPS-A induced cell cycle arrest, which led to a loss of mitochondrial function of the A431 cells and an increase in necrotic and late apoptotic cells. In order to evaluate the apoptosis and cell viability, acridine orange/ethidium bromide staining was used, morphological changes were observed using fluorescence microscopy and typical apoptotic characteristics were observed. Following treatment with a high dose of EPS-A, transmission electron microscopy showed nuclear fragmentation, chromosome condensation, cell shrinkage and expansion of the endoplasmic reticulum; apoptotic bodies were also observed. In conclusion, EPS-A caused cell cycle arrest, stimulated cell apoptosis via the mitochondrial pathway and exhibited important anti-cancer activity. |
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In the present study, A431 human epidermoid carcinoma cells were selected as target cells and cultivated in vitro as an experimental model to investigate the anti-cancer effect of extracellular polymeric substances from Aphanizomenon flos-aquae (EPS-A) and the possible underlying mechanism. Apoptosis- and cell cycle-associated molecules as well as the mitochondrial membrane potential of the cells were quantified using flow cytometry (FCM). FCM showed that EPS-A induced cell cycle arrest, which led to a loss of mitochondrial function of the A431 cells and an increase in necrotic and late apoptotic cells. In order to evaluate the apoptosis and cell viability, acridine orange/ethidium bromide staining was used, morphological changes were observed using fluorescence microscopy and typical apoptotic characteristics were observed. Following treatment with a high dose of EPS-A, transmission electron microscopy showed nuclear fragmentation, chromosome condensation, cell shrinkage and expansion of the endoplasmic reticulum; apoptotic bodies were also observed. In conclusion, EPS-A caused cell cycle arrest, stimulated cell apoptosis via the mitochondrial pathway and exhibited important anti-cancer activity.</description><identifier>ISSN: 1792-0981</identifier><identifier>EISSN: 1792-1015</identifier><identifier>DOI: 10.3892/etm.2015.2644</identifier><identifier>PMID: 26622416</identifier><language>eng</language><publisher>Greece: D.A. Spandidos</publisher><subject>anti-cancer ; Aphanizomenon flos-aquae ; Apoptosis ; Cancer therapies ; Cell cycle ; Cell growth ; Cyanobacteria ; Deoxyribonucleic acid ; DNA ; Drug dosages ; Drug therapy ; extracellular polymeric substances ; Genetic aspects ; Health aspects ; human epidermoid carcinoma ; Mitochondria ; Morphology ; Permeability ; Squamous cell carcinoma ; Studies</subject><ispartof>Experimental and therapeutic medicine, 2015-09, Vol.10 (3), p.927-932</ispartof><rights>Copyright: © Xue et al. This is an open access article distributed under the terms of a Creative Commons Attribution License.</rights><rights>COPYRIGHT 2015 Spandidos Publications</rights><rights>Copyright Spandidos Publications UK Ltd. 2015</rights><rights>Copyright: © Xue et al. This is an open access article distributed under the terms of a Creative Commons Attribution License. 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c512t-46ff2511b168574156f84914e2203429e8f07912c04371ed761f64e1a55ab1683</citedby><cites>FETCH-LOGICAL-c512t-46ff2511b168574156f84914e2203429e8f07912c04371ed761f64e1a55ab1683</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4533141/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4533141/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26622416$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>XUE, XING</creatorcontrib><creatorcontrib>LV, YING</creatorcontrib><creatorcontrib>LIU, QING</creatorcontrib><creatorcontrib>ZHANG, XIAOLAN</creatorcontrib><creatorcontrib>ZHAO, YOUHONG</creatorcontrib><creatorcontrib>ZHANG, LILI</creatorcontrib><creatorcontrib>XU, SHIYUAN</creatorcontrib><title>Extracellular polymeric substance from Aphanizomenon flos-aquae induces apoptosis via the mitochondrial pathway in A431 human epidermoid carcinoma cells</title><title>Experimental and therapeutic medicine</title><addtitle>Exp Ther Med</addtitle><description>Extracellular polymeric substance (EPS) is a substance secreted during algal growth, which has been found to have numerous health-promoting effects. In the present study, A431 human epidermoid carcinoma cells were selected as target cells and cultivated in vitro as an experimental model to investigate the anti-cancer effect of extracellular polymeric substances from Aphanizomenon flos-aquae (EPS-A) and the possible underlying mechanism. Apoptosis- and cell cycle-associated molecules as well as the mitochondrial membrane potential of the cells were quantified using flow cytometry (FCM). FCM showed that EPS-A induced cell cycle arrest, which led to a loss of mitochondrial function of the A431 cells and an increase in necrotic and late apoptotic cells. In order to evaluate the apoptosis and cell viability, acridine orange/ethidium bromide staining was used, morphological changes were observed using fluorescence microscopy and typical apoptotic characteristics were observed. Following treatment with a high dose of EPS-A, transmission electron microscopy showed nuclear fragmentation, chromosome condensation, cell shrinkage and expansion of the endoplasmic reticulum; apoptotic bodies were also observed. In conclusion, EPS-A caused cell cycle arrest, stimulated cell apoptosis via the mitochondrial pathway and exhibited important anti-cancer activity.</description><subject>anti-cancer</subject><subject>Aphanizomenon flos-aquae</subject><subject>Apoptosis</subject><subject>Cancer therapies</subject><subject>Cell cycle</subject><subject>Cell growth</subject><subject>Cyanobacteria</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>Drug dosages</subject><subject>Drug therapy</subject><subject>extracellular polymeric substances</subject><subject>Genetic aspects</subject><subject>Health aspects</subject><subject>human epidermoid carcinoma</subject><subject>Mitochondria</subject><subject>Morphology</subject><subject>Permeability</subject><subject>Squamous cell carcinoma</subject><subject>Studies</subject><issn>1792-0981</issn><issn>1792-1015</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNptksFu1DAQhiMEolXpkSuyhJC4ZMk4tpNckFbVFpCKuJSz5XUmjavYTu2ksDxJHxeHXRaK8Bxsjb_55Rn_WfYSilVZN_QdTnZFC-ArKhh7kp1C1dAcUuLp4Vw0NZxk5zHeFmlxAXXNn2cnVAhKGYjT7GHzfQpK4zDMgwpk9MPOYjCaxHkbJ-U0ki54S9Zjr5z54S0670g3-Jiru1khMa6dNUaiRj9OPppI7o0iU4_Emsnr3rs2GDWQUU39N7VLPFmzEkg_W-UIjqbFYL1piVZBG-etIstr4ovsWaeGiOeH_Sz7erm5vviYX3358OlifZVrDnTKmeg6ygG2IGpeMeCiq1kDDCktSkYbrLuiaoDqgpUVYFsJ6ARDUJyrpaY8y97vdcd5a7HV6NI8BjkGY1XYSa-MfHzjTC9v_L1kvCyBQRJ4exAI_m7GOElr4tKCcujnKKFO02ac11VCX_-D3vo5uNSehKZM_1aXgv-hbtSA0rjOLz-0iMo0OVoIVhc0Uav_UClatEZ7h51J-UcF-b5ABx9jwO7YIxRycZNMbpKLm-TipsS_-nswR_q3dxLwZg_EUbnWtD4emc3157xI8UvoJwyT0kA</recordid><startdate>20150901</startdate><enddate>20150901</enddate><creator>XUE, XING</creator><creator>LV, YING</creator><creator>LIU, QING</creator><creator>ZHANG, XIAOLAN</creator><creator>ZHAO, YOUHONG</creator><creator>ZHANG, LILI</creator><creator>XU, SHIYUAN</creator><general>D.A. 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In the present study, A431 human epidermoid carcinoma cells were selected as target cells and cultivated in vitro as an experimental model to investigate the anti-cancer effect of extracellular polymeric substances from Aphanizomenon flos-aquae (EPS-A) and the possible underlying mechanism. Apoptosis- and cell cycle-associated molecules as well as the mitochondrial membrane potential of the cells were quantified using flow cytometry (FCM). FCM showed that EPS-A induced cell cycle arrest, which led to a loss of mitochondrial function of the A431 cells and an increase in necrotic and late apoptotic cells. In order to evaluate the apoptosis and cell viability, acridine orange/ethidium bromide staining was used, morphological changes were observed using fluorescence microscopy and typical apoptotic characteristics were observed. Following treatment with a high dose of EPS-A, transmission electron microscopy showed nuclear fragmentation, chromosome condensation, cell shrinkage and expansion of the endoplasmic reticulum; apoptotic bodies were also observed. In conclusion, EPS-A caused cell cycle arrest, stimulated cell apoptosis via the mitochondrial pathway and exhibited important anti-cancer activity.</abstract><cop>Greece</cop><pub>D.A. Spandidos</pub><pmid>26622416</pmid><doi>10.3892/etm.2015.2644</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | anti-cancer Aphanizomenon flos-aquae Apoptosis Cancer therapies Cell cycle Cell growth Cyanobacteria Deoxyribonucleic acid DNA Drug dosages Drug therapy extracellular polymeric substances Genetic aspects Health aspects human epidermoid carcinoma Mitochondria Morphology Permeability Squamous cell carcinoma Studies |
title | Extracellular polymeric substance from Aphanizomenon flos-aquae induces apoptosis via the mitochondrial pathway in A431 human epidermoid carcinoma cells |
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