Combined therapy of oncolytic Newcastle disease virus and rhizomes extract of Rheum ribes enhances cancer virotherapy in vitro and in vivo
Phytotherapy has been used to treat a different type of diseases including cancer for a long time, and it was a source for different active anti-tumor agents. Oncolytic Newcastle disease virus (AMHA1) are very promising anti-tumor therapy. Nevertheless, NDV-based monotherapeutics have not been very...
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description | Phytotherapy has been used to treat a different type of diseases including cancer for a long time, and it was a source for different active anti-tumor agents. Oncolytic Newcastle disease virus (AMHA1) are very promising anti-tumor therapy. Nevertheless, NDV-based monotherapeutics have not been very useful to some resistant tumors. Thus, the efficiency of oncolytic NDV must enhance by combining NDV with other novel therapies. The current study aimed to determine the possibility of improving the oncolytic effect induced by NDV through
Rheum ribes
rhizomes extract administration in vitro and in vivo. Methods, the in vitro study include exposure of the crude extract of
Rheum ribes
alone or NDV alone or combination of both agents for 72 h. The cancer cells tested were murine mammary adenocarcinoma AMN3, Human Rhabdomyosarcoma RD, and Human Glioblastoma AMGM5, and using rat embryo fibroblast REF as normal control cells. MTT cell viability assay was used and analyzed for possible synergism using the Chou–Talalay analysis method. In vivo experiment included study the combination and the monotherapeutic modalities in the transplanted murine mammary adenocarcinoma AM3 line and tumor sections analyzed by histopathology. Results, Combination therapy of NDV–
R. ribes
showed enhanced oncolytic activity on cancer cells. With no cytotoxicity on normal cells. In vivo study showed that monotherapeutic modalities had lower growth inhibitory effect on transplanted tumors in mice in compare to combination therapy. Histopathological examination revealed the broader area of necrosis in tumors treated by combination therapy. In conclusion, the novel combination recommended for clinical application for cancer therapy. |
doi_str_mv | 10.1007/s11033-020-05259-z |
format | Article |
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Rheum ribes
rhizomes extract administration in vitro and in vivo. Methods, the in vitro study include exposure of the crude extract of
Rheum ribes
alone or NDV alone or combination of both agents for 72 h. The cancer cells tested were murine mammary adenocarcinoma AMN3, Human Rhabdomyosarcoma RD, and Human Glioblastoma AMGM5, and using rat embryo fibroblast REF as normal control cells. MTT cell viability assay was used and analyzed for possible synergism using the Chou–Talalay analysis method. In vivo experiment included study the combination and the monotherapeutic modalities in the transplanted murine mammary adenocarcinoma AM3 line and tumor sections analyzed by histopathology. Results, Combination therapy of NDV–
R. ribes
showed enhanced oncolytic activity on cancer cells. With no cytotoxicity on normal cells. In vivo study showed that monotherapeutic modalities had lower growth inhibitory effect on transplanted tumors in mice in compare to combination therapy. Histopathological examination revealed the broader area of necrosis in tumors treated by combination therapy. In conclusion, the novel combination recommended for clinical application for cancer therapy.</description><identifier>ISSN: 0301-4851</identifier><identifier>EISSN: 1573-4978</identifier><identifier>DOI: 10.1007/s11033-020-05259-z</identifier><identifier>PMID: 31970625</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Adenocarcinoma ; Adenocarcinoma - pathology ; Adenocarcinoma - therapy ; Animal Anatomy ; Animal Biochemistry ; Animals ; Antineoplastic Agents - pharmacology ; Biochemistry & Molecular Biology ; Biomedical and Life Sciences ; Brain cancer ; Cancer ; Cell Line ; Cell Line, Tumor ; Cell Survival - drug effects ; Cell viability ; Combined Modality Therapy - methods ; Cytotoxicity ; Female ; Glioblastoma ; Histology ; Humans ; Life Sciences ; Life Sciences & Biomedicine ; Mammary Neoplasms, Experimental - pathology ; Mammary Neoplasms, Experimental - therapy ; Mice ; Morphology ; Newcastle disease ; Newcastle disease virus - physiology ; Oncolysis ; Oncolytic Virotherapy - methods ; Oncolytic Viruses - physiology ; Original Article ; Phytotherapy ; Plant Extracts - pharmacology ; Rats ; Rhabdomyosarcoma ; Rheum - chemistry ; Rhizome - chemistry ; Rhizomes ; Science & Technology ; Treatment Outcome ; Tumors</subject><ispartof>Molecular biology reports, 2020-03, Vol.47 (3), p.1691-1702</ispartof><rights>Springer Nature B.V. 2020</rights><rights>Molecular Biology Reports is a copyright of Springer, (2020). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>12</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000508695900003</woscitedreferencesoriginalsourcerecordid><citedby>FETCH-LOGICAL-c375t-20ed8f42b157e56ee284fab903ffc9229dda4c401db0f7c611f651ba70811b613</citedby><cites>FETCH-LOGICAL-c375t-20ed8f42b157e56ee284fab903ffc9229dda4c401db0f7c611f651ba70811b613</cites><orcidid>0000-0003-2574-9109 ; 0000-0002-2699-1514</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11033-020-05259-z$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11033-020-05259-z$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>315,782,786,27931,27932,28255,41495,42564,51326</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31970625$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Al-Shammari, Ahmed Majeed</creatorcontrib><creatorcontrib>Jalill, Raghad Dhyea Abdul</creatorcontrib><creatorcontrib>Hussein, Mohammed F.</creatorcontrib><title>Combined therapy of oncolytic Newcastle disease virus and rhizomes extract of Rheum ribes enhances cancer virotherapy in vitro and in vivo</title><title>Molecular biology reports</title><addtitle>Mol Biol Rep</addtitle><addtitle>MOL BIOL REP</addtitle><addtitle>Mol Biol Rep</addtitle><description>Phytotherapy has been used to treat a different type of diseases including cancer for a long time, and it was a source for different active anti-tumor agents. Oncolytic Newcastle disease virus (AMHA1) are very promising anti-tumor therapy. Nevertheless, NDV-based monotherapeutics have not been very useful to some resistant tumors. Thus, the efficiency of oncolytic NDV must enhance by combining NDV with other novel therapies. The current study aimed to determine the possibility of improving the oncolytic effect induced by NDV through
Rheum ribes
rhizomes extract administration in vitro and in vivo. Methods, the in vitro study include exposure of the crude extract of
Rheum ribes
alone or NDV alone or combination of both agents for 72 h. The cancer cells tested were murine mammary adenocarcinoma AMN3, Human Rhabdomyosarcoma RD, and Human Glioblastoma AMGM5, and using rat embryo fibroblast REF as normal control cells. MTT cell viability assay was used and analyzed for possible synergism using the Chou–Talalay analysis method. In vivo experiment included study the combination and the monotherapeutic modalities in the transplanted murine mammary adenocarcinoma AM3 line and tumor sections analyzed by histopathology. Results, Combination therapy of NDV–
R. ribes
showed enhanced oncolytic activity on cancer cells. With no cytotoxicity on normal cells. In vivo study showed that monotherapeutic modalities had lower growth inhibitory effect on transplanted tumors in mice in compare to combination therapy. Histopathological examination revealed the broader area of necrosis in tumors treated by combination therapy. In conclusion, the novel combination recommended for clinical application for cancer therapy.</description><subject>Adenocarcinoma</subject><subject>Adenocarcinoma - pathology</subject><subject>Adenocarcinoma - therapy</subject><subject>Animal Anatomy</subject><subject>Animal Biochemistry</subject><subject>Animals</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Biochemistry & Molecular Biology</subject><subject>Biomedical and Life Sciences</subject><subject>Brain cancer</subject><subject>Cancer</subject><subject>Cell Line</subject><subject>Cell Line, Tumor</subject><subject>Cell Survival - drug effects</subject><subject>Cell viability</subject><subject>Combined Modality Therapy - methods</subject><subject>Cytotoxicity</subject><subject>Female</subject><subject>Glioblastoma</subject><subject>Histology</subject><subject>Humans</subject><subject>Life Sciences</subject><subject>Life Sciences & Biomedicine</subject><subject>Mammary Neoplasms, Experimental - pathology</subject><subject>Mammary Neoplasms, Experimental - therapy</subject><subject>Mice</subject><subject>Morphology</subject><subject>Newcastle disease</subject><subject>Newcastle disease virus - physiology</subject><subject>Oncolysis</subject><subject>Oncolytic Virotherapy - methods</subject><subject>Oncolytic Viruses - physiology</subject><subject>Original Article</subject><subject>Phytotherapy</subject><subject>Plant Extracts - pharmacology</subject><subject>Rats</subject><subject>Rhabdomyosarcoma</subject><subject>Rheum - chemistry</subject><subject>Rhizome - chemistry</subject><subject>Rhizomes</subject><subject>Science & Technology</subject><subject>Treatment Outcome</subject><subject>Tumors</subject><issn>0301-4851</issn><issn>1573-4978</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>AOWDO</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>eNqNkd-K1DAUxoso7rj6Al5IwRtBqidJ0zSXMvgPFgXR65KmJ06WNhmTdNeZR_CpTae7K3ghXp2T8Pu-nJOvKJ4SeEUAxOtICDBWAYUKOOWyOt4rNoQLVtVStPeLDTAgVd1yclY8ivESAGoi-MPijBEpoKF8U_za-qm3Docy7TCo_aH0pvRO-_GQrC4_4bVWMY1YDjaiilhe2TDHUrmhDDt79BPGEn-moHRalF92OE9lsP1y7XbK6dzopYRF6W8fsS4fU_Ano9Phyj8uHhg1RnxyU8-Lb-_eft1-qC4-v_-4fXNRaSZ4qijg0Jqa9nlT5A0ibWujegnMGC0plcOgal0DGXowQjeEmIaTXgloCekbws6LF6vvPvgfM8bUTTZqHEfl0M-xo6yusw2hbUaf_4Ve-jm4PF2mBAiQki8UXSkdfIwBTbcPdlLh0BHolqS6NakuJ9WdkuqOWfTsxnruJxzuJLfRZKBdgWvsvYnaYv7FOyxnyaFtJJe5A7a1SSXr3dbPLmXpy_-XZpqtdMyE-47hz5L_mP83q__BvQ</recordid><startdate>20200301</startdate><enddate>20200301</enddate><creator>Al-Shammari, Ahmed Majeed</creator><creator>Jalill, Raghad Dhyea Abdul</creator><creator>Hussein, Mohammed F.</creator><general>Springer Netherlands</general><general>Springer Nature</general><general>Springer Nature B.V</general><scope>AOWDO</scope><scope>BLEPL</scope><scope>DTL</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>7TK</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</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>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-2574-9109</orcidid><orcidid>https://orcid.org/0000-0002-2699-1514</orcidid></search><sort><creationdate>20200301</creationdate><title>Combined therapy of oncolytic Newcastle disease virus and rhizomes extract of Rheum ribes enhances cancer virotherapy in vitro and in vivo</title><author>Al-Shammari, Ahmed Majeed ; Jalill, Raghad Dhyea Abdul ; Hussein, Mohammed F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-20ed8f42b157e56ee284fab903ffc9229dda4c401db0f7c611f651ba70811b613</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Adenocarcinoma</topic><topic>Adenocarcinoma - pathology</topic><topic>Adenocarcinoma - therapy</topic><topic>Animal Anatomy</topic><topic>Animal Biochemistry</topic><topic>Animals</topic><topic>Antineoplastic Agents - pharmacology</topic><topic>Biochemistry & Molecular Biology</topic><topic>Biomedical and Life Sciences</topic><topic>Brain cancer</topic><topic>Cancer</topic><topic>Cell Line</topic><topic>Cell Line, Tumor</topic><topic>Cell Survival - drug effects</topic><topic>Cell viability</topic><topic>Combined Modality Therapy - methods</topic><topic>Cytotoxicity</topic><topic>Female</topic><topic>Glioblastoma</topic><topic>Histology</topic><topic>Humans</topic><topic>Life Sciences</topic><topic>Life Sciences & Biomedicine</topic><topic>Mammary Neoplasms, Experimental - pathology</topic><topic>Mammary Neoplasms, Experimental - therapy</topic><topic>Mice</topic><topic>Morphology</topic><topic>Newcastle disease</topic><topic>Newcastle disease virus - physiology</topic><topic>Oncolysis</topic><topic>Oncolytic Virotherapy - methods</topic><topic>Oncolytic Viruses - physiology</topic><topic>Original Article</topic><topic>Phytotherapy</topic><topic>Plant Extracts - pharmacology</topic><topic>Rats</topic><topic>Rhabdomyosarcoma</topic><topic>Rheum - chemistry</topic><topic>Rhizome - chemistry</topic><topic>Rhizomes</topic><topic>Science & Technology</topic><topic>Treatment Outcome</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Al-Shammari, Ahmed Majeed</creatorcontrib><creatorcontrib>Jalill, Raghad Dhyea Abdul</creatorcontrib><creatorcontrib>Hussein, Mohammed F.</creatorcontrib><collection>Web of Science - Science Citation Index Expanded - 2020</collection><collection>Web of Science Core Collection</collection><collection>Science Citation Index Expanded</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>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</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 Pharma Collection</collection><collection>Technology Research Database</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 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>Engineering Research Database</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>Biotechnology and BioEngineering Abstracts</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 China</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular biology reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Al-Shammari, Ahmed Majeed</au><au>Jalill, Raghad Dhyea Abdul</au><au>Hussein, Mohammed F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Combined therapy of oncolytic Newcastle disease virus and rhizomes extract of Rheum ribes enhances cancer virotherapy in vitro and in vivo</atitle><jtitle>Molecular biology reports</jtitle><stitle>Mol Biol Rep</stitle><stitle>MOL BIOL REP</stitle><addtitle>Mol Biol Rep</addtitle><date>2020-03-01</date><risdate>2020</risdate><volume>47</volume><issue>3</issue><spage>1691</spage><epage>1702</epage><pages>1691-1702</pages><issn>0301-4851</issn><eissn>1573-4978</eissn><abstract>Phytotherapy has been used to treat a different type of diseases including cancer for a long time, and it was a source for different active anti-tumor agents. Oncolytic Newcastle disease virus (AMHA1) are very promising anti-tumor therapy. Nevertheless, NDV-based monotherapeutics have not been very useful to some resistant tumors. Thus, the efficiency of oncolytic NDV must enhance by combining NDV with other novel therapies. The current study aimed to determine the possibility of improving the oncolytic effect induced by NDV through
Rheum ribes
rhizomes extract administration in vitro and in vivo. Methods, the in vitro study include exposure of the crude extract of
Rheum ribes
alone or NDV alone or combination of both agents for 72 h. The cancer cells tested were murine mammary adenocarcinoma AMN3, Human Rhabdomyosarcoma RD, and Human Glioblastoma AMGM5, and using rat embryo fibroblast REF as normal control cells. MTT cell viability assay was used and analyzed for possible synergism using the Chou–Talalay analysis method. In vivo experiment included study the combination and the monotherapeutic modalities in the transplanted murine mammary adenocarcinoma AM3 line and tumor sections analyzed by histopathology. Results, Combination therapy of NDV–
R. ribes
showed enhanced oncolytic activity on cancer cells. With no cytotoxicity on normal cells. In vivo study showed that monotherapeutic modalities had lower growth inhibitory effect on transplanted tumors in mice in compare to combination therapy. Histopathological examination revealed the broader area of necrosis in tumors treated by combination therapy. In conclusion, the novel combination recommended for clinical application for cancer therapy.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>31970625</pmid><doi>10.1007/s11033-020-05259-z</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0003-2574-9109</orcidid><orcidid>https://orcid.org/0000-0002-2699-1514</orcidid></addata></record> |
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subjects | Adenocarcinoma Adenocarcinoma - pathology Adenocarcinoma - therapy Animal Anatomy Animal Biochemistry Animals Antineoplastic Agents - pharmacology Biochemistry & Molecular Biology Biomedical and Life Sciences Brain cancer Cancer Cell Line Cell Line, Tumor Cell Survival - drug effects Cell viability Combined Modality Therapy - methods Cytotoxicity Female Glioblastoma Histology Humans Life Sciences Life Sciences & Biomedicine Mammary Neoplasms, Experimental - pathology Mammary Neoplasms, Experimental - therapy Mice Morphology Newcastle disease Newcastle disease virus - physiology Oncolysis Oncolytic Virotherapy - methods Oncolytic Viruses - physiology Original Article Phytotherapy Plant Extracts - pharmacology Rats Rhabdomyosarcoma Rheum - chemistry Rhizome - chemistry Rhizomes Science & Technology Treatment Outcome Tumors |
title | Combined therapy of oncolytic Newcastle disease virus and rhizomes extract of Rheum ribes enhances cancer virotherapy in vitro and in vivo |
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