Synergistic Anti-tumour Effects of Quercetin and Oncolytic Adenovirus expressing TRAIL in Human Hepatocellular Carcinoma
The combination of oncolytic adenoviruses and specific chemotherapy agents is fast emerging as a novel therapeutic approach for resistan the patocellular carcinoma (HCC) cells. A detailed analysis of the network between adenovirus and chemotherapeutic agents can help design an effective strategy to...
Gespeichert in:
Veröffentlicht in: | Scientific reports 2018-02, Vol.8 (1), p.2182-8, Article 2182 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 8 |
---|---|
container_issue | 1 |
container_start_page | 2182 |
container_title | Scientific reports |
container_volume | 8 |
creator | Zou, Hai Zheng, Yong-fa Ge, Wei Wang, Shi-bing Mou, Xiao-zhou |
description | The combination of oncolytic adenoviruses and specific chemotherapy agents is fast emerging as a novel therapeutic approach for resistan the patocellular carcinoma (HCC) cells. A detailed analysis of the network between adenovirus and chemotherapeutic agents can help design an effective strategy to combat HCC. We sought to investigate whether a combined treatment of ZD55-TRAIL and quercetin can have an enhanced cell-killing effect on HCC cells.
In-vitro
experiments showed that quercetin can enhance ZD55-TRAIL mediated growth inhibition and apoptosis in HCC cells. In addition, we showed that quercetin reduced ZD55-TRAIL mediated NF-κB activation and down-regulated its downstream targets, which in turn promoted the pro-apoptotic action of ZD55-TRAIL. Furthermore,
in-vivo
experiments in mice injected with HuH-7 cells resulted in significantly greater reduction in tumour growth and volume following combined ZD55-TRAIL and quercetin treatment. In conclusion, we demonstrated that quercetin could sensitize human HCC cells to apoptosis via ZD55-TRAIL
in-vitro
and
in-vivo
and presented ZD55-TRAIL and quercetin combination as a suitable anti-HCC therapy. |
doi_str_mv | 10.1038/s41598-018-20213-7 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5794998</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1993992698</sourcerecordid><originalsourceid>FETCH-LOGICAL-c474t-44c255471a0c453394525f3f785e5648ea0c30c6ec8a696acf4b0e1632f52ec83</originalsourceid><addsrcrecordid>eNp1kU1rGzEQhkVoSUKaP9BDEfTSy7b63F1dCsYkTcAQ0qZnocizrsKu5OojxP--sp0GtxAdJDHzzCvNvAi9p-QzJbz_kgSVqm8I7RtGGOVNd4ROGRGyYZyxNwf3E3Se0gOpSzIlqDpGJ0xxRSVRp-jpx8ZDXLmUncUzn12TyxRKxBfDADYnHAZ8WyBayM5j45f4xtswbnb4Enx4dLEkDE_rCCk5v8J332fXC1zhqzKZusPa5GBhHMtoIp6baJ0Pk3mH3g5mTHD-fJ6hn5cXd_OrZnHz7Xo-WzRWdCI3QlgmpeioIVZIzpWQTA586HoJshU91DgntgXbm1a1xg7ingBtORskq0F-hr7uddflfoKlBZ-jGfU6usnEjQ7G6X8z3v3Sq_CoZaeEUluBT88CMfwukLKeXNr2YzyEkjRVdZiKtTv043_oQx2lr-3tKN6TVnSVYnvKxpBShOHlM5Torbd6762u3uqdt3pb9OGwjZeSv05WgO-BVFN-BfHg7ddl_wDjhrC3</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1993380647</pqid></control><display><type>article</type><title>Synergistic Anti-tumour Effects of Quercetin and Oncolytic Adenovirus expressing TRAIL in Human Hepatocellular Carcinoma</title><source>MEDLINE</source><source>DOAJ Directory of Open Access Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Springer Nature OA Free Journals</source><source>Nature Free</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><source>Free Full-Text Journals in Chemistry</source><creator>Zou, Hai ; Zheng, Yong-fa ; Ge, Wei ; Wang, Shi-bing ; Mou, Xiao-zhou</creator><creatorcontrib>Zou, Hai ; Zheng, Yong-fa ; Ge, Wei ; Wang, Shi-bing ; Mou, Xiao-zhou</creatorcontrib><description>The combination of oncolytic adenoviruses and specific chemotherapy agents is fast emerging as a novel therapeutic approach for resistan the patocellular carcinoma (HCC) cells. A detailed analysis of the network between adenovirus and chemotherapeutic agents can help design an effective strategy to combat HCC. We sought to investigate whether a combined treatment of ZD55-TRAIL and quercetin can have an enhanced cell-killing effect on HCC cells.
In-vitro
experiments showed that quercetin can enhance ZD55-TRAIL mediated growth inhibition and apoptosis in HCC cells. In addition, we showed that quercetin reduced ZD55-TRAIL mediated NF-κB activation and down-regulated its downstream targets, which in turn promoted the pro-apoptotic action of ZD55-TRAIL. Furthermore,
in-vivo
experiments in mice injected with HuH-7 cells resulted in significantly greater reduction in tumour growth and volume following combined ZD55-TRAIL and quercetin treatment. In conclusion, we demonstrated that quercetin could sensitize human HCC cells to apoptosis via ZD55-TRAIL
in-vitro
and
in-vivo
and presented ZD55-TRAIL and quercetin combination as a suitable anti-HCC therapy.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-018-20213-7</identifier><identifier>PMID: 29391509</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>101/1 ; 13/1 ; 13/2 ; 13/21 ; 14/1 ; 14/63 ; 631/326/596 ; 692/4028/67 ; 692/699/67 ; 82/80 ; Adenoviruses ; Animals ; Antioxidants - therapeutic use ; Apoptosis ; Carcinoma, Hepatocellular - pathology ; Carcinoma, Hepatocellular - therapy ; Cell Proliferation ; Chemotherapy ; Combined treatment ; Drug Combinations ; Growth inhibition ; Hepatocellular carcinoma ; Humanities and Social Sciences ; Humans ; Liver cancer ; Liver Neoplasms - pathology ; Liver Neoplasms - therapy ; Male ; Mice ; Mice, Inbred BALB C ; Mice, Nude ; multidisciplinary ; NF-κB protein ; Oncolysis ; Oncolytic Virotherapy ; Quercetin ; Quercetin - therapeutic use ; Science ; Science (multidisciplinary) ; Signal Transduction ; Tumor Cells, Cultured ; Tumors ; Xenograft Model Antitumor Assays</subject><ispartof>Scientific reports, 2018-02, Vol.8 (1), p.2182-8, Article 2182</ispartof><rights>The Author(s) 2018</rights><rights>2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-44c255471a0c453394525f3f785e5648ea0c30c6ec8a696acf4b0e1632f52ec83</citedby><cites>FETCH-LOGICAL-c474t-44c255471a0c453394525f3f785e5648ea0c30c6ec8a696acf4b0e1632f52ec83</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/PMC5794998/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5794998/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27903,27904,41099,42168,51554,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29391509$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zou, Hai</creatorcontrib><creatorcontrib>Zheng, Yong-fa</creatorcontrib><creatorcontrib>Ge, Wei</creatorcontrib><creatorcontrib>Wang, Shi-bing</creatorcontrib><creatorcontrib>Mou, Xiao-zhou</creatorcontrib><title>Synergistic Anti-tumour Effects of Quercetin and Oncolytic Adenovirus expressing TRAIL in Human Hepatocellular Carcinoma</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>The combination of oncolytic adenoviruses and specific chemotherapy agents is fast emerging as a novel therapeutic approach for resistan the patocellular carcinoma (HCC) cells. A detailed analysis of the network between adenovirus and chemotherapeutic agents can help design an effective strategy to combat HCC. We sought to investigate whether a combined treatment of ZD55-TRAIL and quercetin can have an enhanced cell-killing effect on HCC cells.
In-vitro
experiments showed that quercetin can enhance ZD55-TRAIL mediated growth inhibition and apoptosis in HCC cells. In addition, we showed that quercetin reduced ZD55-TRAIL mediated NF-κB activation and down-regulated its downstream targets, which in turn promoted the pro-apoptotic action of ZD55-TRAIL. Furthermore,
in-vivo
experiments in mice injected with HuH-7 cells resulted in significantly greater reduction in tumour growth and volume following combined ZD55-TRAIL and quercetin treatment. In conclusion, we demonstrated that quercetin could sensitize human HCC cells to apoptosis via ZD55-TRAIL
in-vitro
and
in-vivo
and presented ZD55-TRAIL and quercetin combination as a suitable anti-HCC therapy.</description><subject>101/1</subject><subject>13/1</subject><subject>13/2</subject><subject>13/21</subject><subject>14/1</subject><subject>14/63</subject><subject>631/326/596</subject><subject>692/4028/67</subject><subject>692/699/67</subject><subject>82/80</subject><subject>Adenoviruses</subject><subject>Animals</subject><subject>Antioxidants - therapeutic use</subject><subject>Apoptosis</subject><subject>Carcinoma, Hepatocellular - pathology</subject><subject>Carcinoma, Hepatocellular - therapy</subject><subject>Cell Proliferation</subject><subject>Chemotherapy</subject><subject>Combined treatment</subject><subject>Drug Combinations</subject><subject>Growth inhibition</subject><subject>Hepatocellular carcinoma</subject><subject>Humanities and Social Sciences</subject><subject>Humans</subject><subject>Liver cancer</subject><subject>Liver Neoplasms - pathology</subject><subject>Liver Neoplasms - therapy</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Nude</subject><subject>multidisciplinary</subject><subject>NF-κB protein</subject><subject>Oncolysis</subject><subject>Oncolytic Virotherapy</subject><subject>Quercetin</subject><subject>Quercetin - therapeutic use</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Signal Transduction</subject><subject>Tumor Cells, Cultured</subject><subject>Tumors</subject><subject>Xenograft Model Antitumor Assays</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp1kU1rGzEQhkVoSUKaP9BDEfTSy7b63F1dCsYkTcAQ0qZnocizrsKu5OojxP--sp0GtxAdJDHzzCvNvAi9p-QzJbz_kgSVqm8I7RtGGOVNd4ROGRGyYZyxNwf3E3Se0gOpSzIlqDpGJ0xxRSVRp-jpx8ZDXLmUncUzn12TyxRKxBfDADYnHAZ8WyBayM5j45f4xtswbnb4Enx4dLEkDE_rCCk5v8J332fXC1zhqzKZusPa5GBhHMtoIp6baJ0Pk3mH3g5mTHD-fJ6hn5cXd_OrZnHz7Xo-WzRWdCI3QlgmpeioIVZIzpWQTA586HoJshU91DgntgXbm1a1xg7ingBtORskq0F-hr7uddflfoKlBZ-jGfU6usnEjQ7G6X8z3v3Sq_CoZaeEUluBT88CMfwukLKeXNr2YzyEkjRVdZiKtTv043_oQx2lr-3tKN6TVnSVYnvKxpBShOHlM5Torbd6762u3uqdt3pb9OGwjZeSv05WgO-BVFN-BfHg7ddl_wDjhrC3</recordid><startdate>20180201</startdate><enddate>20180201</enddate><creator>Zou, Hai</creator><creator>Zheng, Yong-fa</creator><creator>Ge, Wei</creator><creator>Wang, Shi-bing</creator><creator>Mou, Xiao-zhou</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</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>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20180201</creationdate><title>Synergistic Anti-tumour Effects of Quercetin and Oncolytic Adenovirus expressing TRAIL in Human Hepatocellular Carcinoma</title><author>Zou, Hai ; Zheng, Yong-fa ; Ge, Wei ; Wang, Shi-bing ; Mou, Xiao-zhou</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-44c255471a0c453394525f3f785e5648ea0c30c6ec8a696acf4b0e1632f52ec83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>101/1</topic><topic>13/1</topic><topic>13/2</topic><topic>13/21</topic><topic>14/1</topic><topic>14/63</topic><topic>631/326/596</topic><topic>692/4028/67</topic><topic>692/699/67</topic><topic>82/80</topic><topic>Adenoviruses</topic><topic>Animals</topic><topic>Antioxidants - therapeutic use</topic><topic>Apoptosis</topic><topic>Carcinoma, Hepatocellular - pathology</topic><topic>Carcinoma, Hepatocellular - therapy</topic><topic>Cell Proliferation</topic><topic>Chemotherapy</topic><topic>Combined treatment</topic><topic>Drug Combinations</topic><topic>Growth inhibition</topic><topic>Hepatocellular carcinoma</topic><topic>Humanities and Social Sciences</topic><topic>Humans</topic><topic>Liver cancer</topic><topic>Liver Neoplasms - pathology</topic><topic>Liver Neoplasms - therapy</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Nude</topic><topic>multidisciplinary</topic><topic>NF-κB protein</topic><topic>Oncolysis</topic><topic>Oncolytic Virotherapy</topic><topic>Quercetin</topic><topic>Quercetin - therapeutic use</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><topic>Signal Transduction</topic><topic>Tumor Cells, Cultured</topic><topic>Tumors</topic><topic>Xenograft Model Antitumor Assays</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zou, Hai</creatorcontrib><creatorcontrib>Zheng, Yong-fa</creatorcontrib><creatorcontrib>Ge, Wei</creatorcontrib><creatorcontrib>Wang, Shi-bing</creatorcontrib><creatorcontrib>Mou, Xiao-zhou</creatorcontrib><collection>Springer Nature OA Free Journals</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>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech 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 Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</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>Science Database</collection><collection>Biological Science Database</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>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zou, Hai</au><au>Zheng, Yong-fa</au><au>Ge, Wei</au><au>Wang, Shi-bing</au><au>Mou, Xiao-zhou</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synergistic Anti-tumour Effects of Quercetin and Oncolytic Adenovirus expressing TRAIL in Human Hepatocellular Carcinoma</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2018-02-01</date><risdate>2018</risdate><volume>8</volume><issue>1</issue><spage>2182</spage><epage>8</epage><pages>2182-8</pages><artnum>2182</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>The combination of oncolytic adenoviruses and specific chemotherapy agents is fast emerging as a novel therapeutic approach for resistan the patocellular carcinoma (HCC) cells. A detailed analysis of the network between adenovirus and chemotherapeutic agents can help design an effective strategy to combat HCC. We sought to investigate whether a combined treatment of ZD55-TRAIL and quercetin can have an enhanced cell-killing effect on HCC cells.
In-vitro
experiments showed that quercetin can enhance ZD55-TRAIL mediated growth inhibition and apoptosis in HCC cells. In addition, we showed that quercetin reduced ZD55-TRAIL mediated NF-κB activation and down-regulated its downstream targets, which in turn promoted the pro-apoptotic action of ZD55-TRAIL. Furthermore,
in-vivo
experiments in mice injected with HuH-7 cells resulted in significantly greater reduction in tumour growth and volume following combined ZD55-TRAIL and quercetin treatment. In conclusion, we demonstrated that quercetin could sensitize human HCC cells to apoptosis via ZD55-TRAIL
in-vitro
and
in-vivo
and presented ZD55-TRAIL and quercetin combination as a suitable anti-HCC therapy.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>29391509</pmid><doi>10.1038/s41598-018-20213-7</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2045-2322 |
ispartof | Scientific reports, 2018-02, Vol.8 (1), p.2182-8, Article 2182 |
issn | 2045-2322 2045-2322 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5794998 |
source | MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Springer Nature OA Free Journals; Nature Free; PubMed Central; Alma/SFX Local Collection; Free Full-Text Journals in Chemistry |
subjects | 101/1 13/1 13/2 13/21 14/1 14/63 631/326/596 692/4028/67 692/699/67 82/80 Adenoviruses Animals Antioxidants - therapeutic use Apoptosis Carcinoma, Hepatocellular - pathology Carcinoma, Hepatocellular - therapy Cell Proliferation Chemotherapy Combined treatment Drug Combinations Growth inhibition Hepatocellular carcinoma Humanities and Social Sciences Humans Liver cancer Liver Neoplasms - pathology Liver Neoplasms - therapy Male Mice Mice, Inbred BALB C Mice, Nude multidisciplinary NF-κB protein Oncolysis Oncolytic Virotherapy Quercetin Quercetin - therapeutic use Science Science (multidisciplinary) Signal Transduction Tumor Cells, Cultured Tumors Xenograft Model Antitumor Assays |
title | Synergistic Anti-tumour Effects of Quercetin and Oncolytic Adenovirus expressing TRAIL in Human Hepatocellular Carcinoma |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-25T21%3A23%3A59IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Synergistic%20Anti-tumour%20Effects%20of%20Quercetin%20and%20Oncolytic%20Adenovirus%20expressing%20TRAIL%20in%20Human%20Hepatocellular%20Carcinoma&rft.jtitle=Scientific%20reports&rft.au=Zou,%20Hai&rft.date=2018-02-01&rft.volume=8&rft.issue=1&rft.spage=2182&rft.epage=8&rft.pages=2182-8&rft.artnum=2182&rft.issn=2045-2322&rft.eissn=2045-2322&rft_id=info:doi/10.1038/s41598-018-20213-7&rft_dat=%3Cproquest_pubme%3E1993992698%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1993380647&rft_id=info:pmid/29391509&rfr_iscdi=true |