Antitumor Activity of Ficus deltoidea Extract on Oral Cancer: An In Vivo Study
Background. The aim of this study is to evaluate the chemopreventive and chemotherapeutic activities of Ficus deltoidea (FD) in an animal model induced for oral cancer using 4-nitroquinoline-1-oxide (4NQO). Methods. Male Sprague-Dawley (SD) rats were randomized into six groups (n = 7 per group): Gro...
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description | Background. The aim of this study is to evaluate the chemopreventive and chemotherapeutic activities of Ficus deltoidea (FD) in an animal model induced for oral cancer using 4-nitroquinoline-1-oxide (4NQO). Methods. Male Sprague-Dawley (SD) rats were randomized into six groups (n = 7 per group): Group 1 (untreated group); Group 2 (control cancer group) received 4NQO only for 8 weeks in their drinking water; Groups 3 and 4 (chemopreventive) received 4NQO for 8 weeks and were simultaneously treated with FD extract at 250 and 500 mg/kg, respectively, by oral gavage; Groups 5 and 6 (chemotherapeutic) received 4NQO for 8 weeks followed by the administration of FD extract at 250 and 500 mg/kg, respectively, for another 10 weeks. The incidence of oral cancer was microscopically evaluated. Moreover, immunohistochemical expression was analysed in tongue specimens using an image analyser computer system, while the RT2 profiler PCR array method was employed for gene expression analysis. Results. The results of the present study showed a beneficial regression effect of the FD extract on tumor progression. The FD extract significantly reduced the incidence of oral squamous cell carcinoma (OSCC) from 100% to 14.3% in the high-dose groups. The immunohistochemical analysis showed that the FD extract had significantly decreased the expression of the key tumor marker cyclin D1 and had significantly increased the expression of the β-catenin and e-cadherin antibodies that are associated with enhanced cellular adhesion. Based on the gene expression analysis, FD extract had reduced the expression of the TWIST1 and RAC1 genes associated with epithelial-mesenchymal transition (EMT) and had significantly downregulated the COX-2 and EGFR genes associated with cancer angiogenesis, metastasis, and chemoresistance. Our data suggest that the FD extract exerts chemopreventive and chemotherapeutic activities in an animal model induced for oral cancer using 4NQO, thus having the potential to be developed as chemopreventive and chemotherapeutic agents. |
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The aim of this study is to evaluate the chemopreventive and chemotherapeutic activities of Ficus deltoidea (FD) in an animal model induced for oral cancer using 4-nitroquinoline-1-oxide (4NQO). Methods. Male Sprague-Dawley (SD) rats were randomized into six groups (n = 7 per group): Group 1 (untreated group); Group 2 (control cancer group) received 4NQO only for 8 weeks in their drinking water; Groups 3 and 4 (chemopreventive) received 4NQO for 8 weeks and were simultaneously treated with FD extract at 250 and 500 mg/kg, respectively, by oral gavage; Groups 5 and 6 (chemotherapeutic) received 4NQO for 8 weeks followed by the administration of FD extract at 250 and 500 mg/kg, respectively, for another 10 weeks. The incidence of oral cancer was microscopically evaluated. Moreover, immunohistochemical expression was analysed in tongue specimens using an image analyser computer system, while the RT2 profiler PCR array method was employed for gene expression analysis. Results. The results of the present study showed a beneficial regression effect of the FD extract on tumor progression. The FD extract significantly reduced the incidence of oral squamous cell carcinoma (OSCC) from 100% to 14.3% in the high-dose groups. The immunohistochemical analysis showed that the FD extract had significantly decreased the expression of the key tumor marker cyclin D1 and had significantly increased the expression of the β-catenin and e-cadherin antibodies that are associated with enhanced cellular adhesion. Based on the gene expression analysis, FD extract had reduced the expression of the TWIST1 and RAC1 genes associated with epithelial-mesenchymal transition (EMT) and had significantly downregulated the COX-2 and EGFR genes associated with cancer angiogenesis, metastasis, and chemoresistance. Our data suggest that the FD extract exerts chemopreventive and chemotherapeutic activities in an animal model induced for oral cancer using 4NQO, thus having the potential to be developed as chemopreventive and chemotherapeutic agents.</description><identifier>ISSN: 1687-8450</identifier><identifier>EISSN: 1687-8450</identifier><identifier>EISSN: 1687-8469</identifier><identifier>DOI: 10.1155/2020/5490468</identifier><identifier>PMID: 32104177</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><subject>Antioxidants ; Cancer ; Cancer therapies ; Chemotherapy ; Cloning ; Development and progression ; Drinking water ; Drug dosages ; Gene expression ; Laboratory animals ; Medical research ; Metastasis ; Mouth cancer ; Natural products ; Oncology, Experimental ; Oral cancer ; Prevention ; Sperm ; Squamous cell carcinoma ; Tongue</subject><ispartof>Journal of oncology, 2020, Vol.2020 (2020), p.1-10</ispartof><rights>Copyright © 2020 May Al-koshab et al.</rights><rights>COPYRIGHT 2020 John Wiley & Sons, Inc.</rights><rights>Copyright © 2020 May Al-koshab et al. This work is licensed 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><rights>Copyright © 2020 May Al-koshab et al. 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c461t-6731e41532170d23e9e8a34cb7919128be749e0440b1bec2f87c7c9df6c7b1c23</citedby><cites>FETCH-LOGICAL-c461t-6731e41532170d23e9e8a34cb7919128be749e0440b1bec2f87c7c9df6c7b1c23</cites><orcidid>0000-0002-2353-6655 ; 0000-0003-0048-0000 ; 0000-0001-7358-2994 ; 0000-0001-8981-7567 ; 0000-0002-2284-4314</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7035569/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7035569/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,4024,27923,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32104177$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Adrian, Thomas E.</contributor><contributor>Thomas E Adrian</contributor><creatorcontrib>Ali-Saeed, Rola</creatorcontrib><creatorcontrib>Mohd Bakri, Marina</creatorcontrib><creatorcontrib>Alabsi, Aied Mohammed</creatorcontrib><creatorcontrib>Al-koshab, May</creatorcontrib><creatorcontrib>Subramaniam, Manimalar Selvi Naicker</creatorcontrib><title>Antitumor Activity of Ficus deltoidea Extract on Oral Cancer: An In Vivo Study</title><title>Journal of oncology</title><addtitle>J Oncol</addtitle><description>Background. The aim of this study is to evaluate the chemopreventive and chemotherapeutic activities of Ficus deltoidea (FD) in an animal model induced for oral cancer using 4-nitroquinoline-1-oxide (4NQO). Methods. Male Sprague-Dawley (SD) rats were randomized into six groups (n = 7 per group): Group 1 (untreated group); Group 2 (control cancer group) received 4NQO only for 8 weeks in their drinking water; Groups 3 and 4 (chemopreventive) received 4NQO for 8 weeks and were simultaneously treated with FD extract at 250 and 500 mg/kg, respectively, by oral gavage; Groups 5 and 6 (chemotherapeutic) received 4NQO for 8 weeks followed by the administration of FD extract at 250 and 500 mg/kg, respectively, for another 10 weeks. The incidence of oral cancer was microscopically evaluated. Moreover, immunohistochemical expression was analysed in tongue specimens using an image analyser computer system, while the RT2 profiler PCR array method was employed for gene expression analysis. Results. The results of the present study showed a beneficial regression effect of the FD extract on tumor progression. The FD extract significantly reduced the incidence of oral squamous cell carcinoma (OSCC) from 100% to 14.3% in the high-dose groups. The immunohistochemical analysis showed that the FD extract had significantly decreased the expression of the key tumor marker cyclin D1 and had significantly increased the expression of the β-catenin and e-cadherin antibodies that are associated with enhanced cellular adhesion. Based on the gene expression analysis, FD extract had reduced the expression of the TWIST1 and RAC1 genes associated with epithelial-mesenchymal transition (EMT) and had significantly downregulated the COX-2 and EGFR genes associated with cancer angiogenesis, metastasis, and chemoresistance. Our data suggest that the FD extract exerts chemopreventive and chemotherapeutic activities in an animal model induced for oral cancer using 4NQO, thus having the potential to be developed as chemopreventive and chemotherapeutic agents.</description><subject>Antioxidants</subject><subject>Cancer</subject><subject>Cancer therapies</subject><subject>Chemotherapy</subject><subject>Cloning</subject><subject>Development and progression</subject><subject>Drinking water</subject><subject>Drug dosages</subject><subject>Gene expression</subject><subject>Laboratory animals</subject><subject>Medical research</subject><subject>Metastasis</subject><subject>Mouth cancer</subject><subject>Natural products</subject><subject>Oncology, Experimental</subject><subject>Oral cancer</subject><subject>Prevention</subject><subject>Sperm</subject><subject>Squamous cell carcinoma</subject><subject>Tongue</subject><issn>1687-8450</issn><issn>1687-8450</issn><issn>1687-8469</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>RHX</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNqNkU1rFTEUhgdRbK3uXEvATUFvm69JJi6E4dJqodiFH9uQyZxpU-YmbZK59f57M9xrW111lQN5eDjnfavqLcFHhNT1McUUH9dcYS6aZ9U-EY1cNLzGzx_Ne9WrlK4xFhwr8bLaY5RgTqTcr761Prs8rUJErc1u7fIGhQGdOjsl1MOYg-vBoJPfORqbUfDoIpoRLY23ED-h1qMzj365dUDf89RvXlcvBjMmeLN7D6qfpyc_ll8X5xdfzpbt-cJyQfJCSEaAk7rsIXFPGShoDOO2k4ooQpsOJFeAOccd6cDSoZFWWtUPwsqOWMoOqs9b783UraC34Mt-o76JbmXiRgfj9L8_3l3py7DWErO6FqoIDneCGG4nSFmvXLIwjsZDmJKmTAjBOOd1Qd__h16HKfpynqYcS8FZyfKBujQjaOeHMCc2S3UrStyYNHR2fdxSNoaUIgz3KxOs5zr1XKfe1Vnwd4_PvIf_9leAD1vgyvne3Lkn6qAwMJgHmjSNUpT9AWTAroc</recordid><startdate>2020</startdate><enddate>2020</enddate><creator>Ali-Saeed, Rola</creator><creator>Mohd Bakri, Marina</creator><creator>Alabsi, Aied Mohammed</creator><creator>Al-koshab, May</creator><creator>Subramaniam, Manimalar Selvi Naicker</creator><general>Hindawi Publishing Corporation</general><general>Hindawi</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>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-2353-6655</orcidid><orcidid>https://orcid.org/0000-0003-0048-0000</orcidid><orcidid>https://orcid.org/0000-0001-7358-2994</orcidid><orcidid>https://orcid.org/0000-0001-8981-7567</orcidid><orcidid>https://orcid.org/0000-0002-2284-4314</orcidid></search><sort><creationdate>2020</creationdate><title>Antitumor Activity of Ficus deltoidea Extract on Oral Cancer: An In Vivo Study</title><author>Ali-Saeed, Rola ; Mohd Bakri, Marina ; Alabsi, Aied Mohammed ; Al-koshab, May ; Subramaniam, Manimalar Selvi Naicker</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c461t-6731e41532170d23e9e8a34cb7919128be749e0440b1bec2f87c7c9df6c7b1c23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Antioxidants</topic><topic>Cancer</topic><topic>Cancer therapies</topic><topic>Chemotherapy</topic><topic>Cloning</topic><topic>Development and progression</topic><topic>Drinking water</topic><topic>Drug dosages</topic><topic>Gene expression</topic><topic>Laboratory animals</topic><topic>Medical research</topic><topic>Metastasis</topic><topic>Mouth cancer</topic><topic>Natural products</topic><topic>Oncology, Experimental</topic><topic>Oral cancer</topic><topic>Prevention</topic><topic>Sperm</topic><topic>Squamous cell carcinoma</topic><topic>Tongue</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ali-Saeed, Rola</creatorcontrib><creatorcontrib>Mohd Bakri, Marina</creatorcontrib><creatorcontrib>Alabsi, Aied Mohammed</creatorcontrib><creatorcontrib>Al-koshab, May</creatorcontrib><creatorcontrib>Subramaniam, Manimalar Selvi Naicker</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>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</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>ProQuest Central</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 Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Nursing & Allied Health Premium</collection><collection>Access via ProQuest (Open Access)</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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ali-Saeed, Rola</au><au>Mohd Bakri, Marina</au><au>Alabsi, Aied Mohammed</au><au>Al-koshab, May</au><au>Subramaniam, Manimalar Selvi Naicker</au><au>Adrian, Thomas E.</au><au>Thomas E Adrian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antitumor Activity of Ficus deltoidea Extract on Oral Cancer: An In Vivo Study</atitle><jtitle>Journal of oncology</jtitle><addtitle>J Oncol</addtitle><date>2020</date><risdate>2020</risdate><volume>2020</volume><issue>2020</issue><spage>1</spage><epage>10</epage><pages>1-10</pages><issn>1687-8450</issn><eissn>1687-8450</eissn><eissn>1687-8469</eissn><abstract>Background. The aim of this study is to evaluate the chemopreventive and chemotherapeutic activities of Ficus deltoidea (FD) in an animal model induced for oral cancer using 4-nitroquinoline-1-oxide (4NQO). Methods. Male Sprague-Dawley (SD) rats were randomized into six groups (n = 7 per group): Group 1 (untreated group); Group 2 (control cancer group) received 4NQO only for 8 weeks in their drinking water; Groups 3 and 4 (chemopreventive) received 4NQO for 8 weeks and were simultaneously treated with FD extract at 250 and 500 mg/kg, respectively, by oral gavage; Groups 5 and 6 (chemotherapeutic) received 4NQO for 8 weeks followed by the administration of FD extract at 250 and 500 mg/kg, respectively, for another 10 weeks. The incidence of oral cancer was microscopically evaluated. Moreover, immunohistochemical expression was analysed in tongue specimens using an image analyser computer system, while the RT2 profiler PCR array method was employed for gene expression analysis. Results. The results of the present study showed a beneficial regression effect of the FD extract on tumor progression. The FD extract significantly reduced the incidence of oral squamous cell carcinoma (OSCC) from 100% to 14.3% in the high-dose groups. The immunohistochemical analysis showed that the FD extract had significantly decreased the expression of the key tumor marker cyclin D1 and had significantly increased the expression of the β-catenin and e-cadherin antibodies that are associated with enhanced cellular adhesion. Based on the gene expression analysis, FD extract had reduced the expression of the TWIST1 and RAC1 genes associated with epithelial-mesenchymal transition (EMT) and had significantly downregulated the COX-2 and EGFR genes associated with cancer angiogenesis, metastasis, and chemoresistance. Our data suggest that the FD extract exerts chemopreventive and chemotherapeutic activities in an animal model induced for oral cancer using 4NQO, thus having the potential to be developed as chemopreventive and chemotherapeutic agents.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Publishing Corporation</pub><pmid>32104177</pmid><doi>10.1155/2020/5490468</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-2353-6655</orcidid><orcidid>https://orcid.org/0000-0003-0048-0000</orcidid><orcidid>https://orcid.org/0000-0001-7358-2994</orcidid><orcidid>https://orcid.org/0000-0001-8981-7567</orcidid><orcidid>https://orcid.org/0000-0002-2284-4314</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Antioxidants Cancer Cancer therapies Chemotherapy Cloning Development and progression Drinking water Drug dosages Gene expression Laboratory animals Medical research Metastasis Mouth cancer Natural products Oncology, Experimental Oral cancer Prevention Sperm Squamous cell carcinoma Tongue |
title | Antitumor Activity of Ficus deltoidea Extract on Oral Cancer: An In Vivo Study |
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