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Formulation of quinoa oil-alginate loaded nanoemulsion and its anticancer efficacy as a therapy for chemically induced breast cancer
Background Quinoa seeds ( Chenopodium quinoa Willd.) have gained interest due to their naturally occurring phytochemicals and antioxidants. They possess potent anticancer properties against human colorectal cancer. Methods and Results: Fatty acids in quinoa oil were studied using gas chromatography-...
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Published in: | Molecular biology reports 2024-12, Vol.51 (1), p.705-705, Article 705 |
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creator | El makawy, Aida I. Mabrouk, Dalia M. Ibrahim, Faten M. Abdel-Aziem, Sekena H. EL-Kader, Heba A.M. Abd Youssef, Dalia A. Sharaf, Hafiza A. Mohammed, Shaimaa E. |
description | Background
Quinoa seeds (
Chenopodium quinoa
Willd.) have gained interest due to their naturally occurring phytochemicals and antioxidants. They possess potent anticancer properties against human colorectal cancer. Methods and Results: Fatty acids in quinoa oil were studied using gas chromatography-mass spectrometry. Rats were used to test the acute oral toxicity of the nanoemulsion loaded with sodium alginate. The DPPH radical scavenging method was employed to assess the nanoemulsion’s ability to scavenge free radicals. It was examined the in vivo anticancer potential of quinoa oil nanoemulsion on rats with breast cancer induced by 7, 12-dimethylbenz (a) anthracene (DMBA). DMBA-breast cancer models received daily quinoa oil nanoemulsions for 30 days. The anticancer effect of the nanoemulsion was assessed by measuring ROS, protein carbonyl, gene expression of anti-oncogenes, and histopathological analysis. Supplying quinoa oil nanoemulsion significantly reduced the increase in serum ROS and PC levels induced in breast cancer tissue. The expression levels of antioncogenes in breast cancer tissue were decreased by the quinoa oil nanoemulsion. Nanoemulsions also improved the cellular morphology of breast tumors. Conclusion: The study results indicate that quinoa oil nanoemulsion has anticancer activity against breast cancer, effectively modulating oxidative stress markers, anti-oncogene expressions, and tissue architecture. It can be inferred from the results that quinoa oil nanoemulsion is a chemoprotective medication that may hinder breast cancer progression in rats. |
doi_str_mv | 10.1007/s11033-024-09619-x |
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Quinoa seeds (
Chenopodium quinoa
Willd.) have gained interest due to their naturally occurring phytochemicals and antioxidants. They possess potent anticancer properties against human colorectal cancer. Methods and Results: Fatty acids in quinoa oil were studied using gas chromatography-mass spectrometry. Rats were used to test the acute oral toxicity of the nanoemulsion loaded with sodium alginate. The DPPH radical scavenging method was employed to assess the nanoemulsion’s ability to scavenge free radicals. It was examined the in vivo anticancer potential of quinoa oil nanoemulsion on rats with breast cancer induced by 7, 12-dimethylbenz (a) anthracene (DMBA). DMBA-breast cancer models received daily quinoa oil nanoemulsions for 30 days. The anticancer effect of the nanoemulsion was assessed by measuring ROS, protein carbonyl, gene expression of anti-oncogenes, and histopathological analysis. Supplying quinoa oil nanoemulsion significantly reduced the increase in serum ROS and PC levels induced in breast cancer tissue. The expression levels of antioncogenes in breast cancer tissue were decreased by the quinoa oil nanoemulsion. Nanoemulsions also improved the cellular morphology of breast tumors. Conclusion: The study results indicate that quinoa oil nanoemulsion has anticancer activity against breast cancer, effectively modulating oxidative stress markers, anti-oncogene expressions, and tissue architecture. It can be inferred from the results that quinoa oil nanoemulsion is a chemoprotective medication that may hinder breast cancer progression in rats.</description><identifier>ISSN: 0301-4851</identifier><identifier>ISSN: 1573-4978</identifier><identifier>EISSN: 1573-4978</identifier><identifier>DOI: 10.1007/s11033-024-09619-x</identifier><identifier>PMID: 38824214</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>acute oral toxicity ; Alginates - chemistry ; Alginates - pharmacology ; Alginic acid ; Animal Anatomy ; Animal Biochemistry ; Animals ; Anthracene ; anthracenes ; Anti-oncogenes ; antineoplastic activity ; Antineoplastic Agents - pharmacology ; Antioxidants - pharmacology ; Antitumor activity ; Biomedical and Life Sciences ; blood serum ; Breast cancer ; breast neoplasms ; Breast Neoplasms - drug therapy ; Breast Neoplasms - pathology ; breasts ; Chenopodium quinoa ; Chenopodium quinoa - chemistry ; Colorectal cancer ; Colorectal carcinoma ; colorectal neoplasms ; drug therapy ; Emulsions ; Female ; Free radicals ; Gas chromatography ; gas chromatography-mass spectrometry ; Gene expression ; Histology ; histopathology ; Humans ; Life Sciences ; Mass spectroscopy ; Morphology ; Nanoemulsions ; Nanoparticles - chemistry ; neoplasm progression ; oils ; Oils & fats ; Original Article ; Oxidative stress ; Oxidative Stress - drug effects ; phytochemicals ; Plant Oils - chemistry ; Plant Oils - pharmacology ; Quinoa ; Rats ; Reactive Oxygen Species - metabolism ; Seeds - chemistry ; Sodium alginate ; Toxicity ; tumor suppressor genes</subject><ispartof>Molecular biology reports, 2024-12, Vol.51 (1), p.705-705, Article 705</ispartof><rights>The Author(s), under exclusive licence to Springer Nature B.V. 2024. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2024. The Author(s), under exclusive licence to Springer Nature B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c359t-5b1d76e00f6f30184229f2ea172f9298bbe584c3157b4ec2ed89aa2e3886bd9f3</cites><orcidid>0000-0001-8335-5381</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38824214$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>El makawy, Aida I.</creatorcontrib><creatorcontrib>Mabrouk, Dalia M.</creatorcontrib><creatorcontrib>Ibrahim, Faten M.</creatorcontrib><creatorcontrib>Abdel-Aziem, Sekena H.</creatorcontrib><creatorcontrib>EL-Kader, Heba A.M. Abd</creatorcontrib><creatorcontrib>Youssef, Dalia A.</creatorcontrib><creatorcontrib>Sharaf, Hafiza A.</creatorcontrib><creatorcontrib>Mohammed, Shaimaa E.</creatorcontrib><title>Formulation of quinoa oil-alginate loaded nanoemulsion and its anticancer efficacy as a therapy for chemically induced breast cancer</title><title>Molecular biology reports</title><addtitle>Mol Biol Rep</addtitle><addtitle>Mol Biol Rep</addtitle><description>Background
Quinoa seeds (
Chenopodium quinoa
Willd.) have gained interest due to their naturally occurring phytochemicals and antioxidants. They possess potent anticancer properties against human colorectal cancer. Methods and Results: Fatty acids in quinoa oil were studied using gas chromatography-mass spectrometry. Rats were used to test the acute oral toxicity of the nanoemulsion loaded with sodium alginate. The DPPH radical scavenging method was employed to assess the nanoemulsion’s ability to scavenge free radicals. It was examined the in vivo anticancer potential of quinoa oil nanoemulsion on rats with breast cancer induced by 7, 12-dimethylbenz (a) anthracene (DMBA). DMBA-breast cancer models received daily quinoa oil nanoemulsions for 30 days. The anticancer effect of the nanoemulsion was assessed by measuring ROS, protein carbonyl, gene expression of anti-oncogenes, and histopathological analysis. Supplying quinoa oil nanoemulsion significantly reduced the increase in serum ROS and PC levels induced in breast cancer tissue. The expression levels of antioncogenes in breast cancer tissue were decreased by the quinoa oil nanoemulsion. Nanoemulsions also improved the cellular morphology of breast tumors. Conclusion: The study results indicate that quinoa oil nanoemulsion has anticancer activity against breast cancer, effectively modulating oxidative stress markers, anti-oncogene expressions, and tissue architecture. It can be inferred from the results that quinoa oil nanoemulsion is a chemoprotective medication that may hinder breast cancer progression in rats.</description><subject>acute oral toxicity</subject><subject>Alginates - chemistry</subject><subject>Alginates - pharmacology</subject><subject>Alginic acid</subject><subject>Animal Anatomy</subject><subject>Animal Biochemistry</subject><subject>Animals</subject><subject>Anthracene</subject><subject>anthracenes</subject><subject>Anti-oncogenes</subject><subject>antineoplastic activity</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Antioxidants - pharmacology</subject><subject>Antitumor activity</subject><subject>Biomedical and Life Sciences</subject><subject>blood serum</subject><subject>Breast cancer</subject><subject>breast neoplasms</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Breast Neoplasms - pathology</subject><subject>breasts</subject><subject>Chenopodium quinoa</subject><subject>Chenopodium quinoa - chemistry</subject><subject>Colorectal cancer</subject><subject>Colorectal carcinoma</subject><subject>colorectal neoplasms</subject><subject>drug therapy</subject><subject>Emulsions</subject><subject>Female</subject><subject>Free radicals</subject><subject>Gas chromatography</subject><subject>gas chromatography-mass spectrometry</subject><subject>Gene expression</subject><subject>Histology</subject><subject>histopathology</subject><subject>Humans</subject><subject>Life Sciences</subject><subject>Mass spectroscopy</subject><subject>Morphology</subject><subject>Nanoemulsions</subject><subject>Nanoparticles - chemistry</subject><subject>neoplasm progression</subject><subject>oils</subject><subject>Oils & fats</subject><subject>Original Article</subject><subject>Oxidative stress</subject><subject>Oxidative Stress - drug effects</subject><subject>phytochemicals</subject><subject>Plant Oils - chemistry</subject><subject>Plant Oils - pharmacology</subject><subject>Quinoa</subject><subject>Rats</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>Seeds - chemistry</subject><subject>Sodium alginate</subject><subject>Toxicity</subject><subject>tumor suppressor genes</subject><issn>0301-4851</issn><issn>1573-4978</issn><issn>1573-4978</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqFkU9rFTEUxYNY7LP6BVxIwI2b2PyfyVKKVaHgpq5DJnPTpswkr8kM9O394OZ1qoILXd2Q-zsnnByE3jD6gVHanVfGqBCEckmo0cyQh2dox1QniDRd_xztqKCMyF6xU_Sy1jtKqWSdeoFORd9zyZncoR-Xuczr5JaYE84B368xZYdznIibbmJyC-ApuxFGnFzK0Nh6RF0acVxqm0v0LnkoGEJoR3_Arl3j5RaK2x9wyAX7W5jbapoOOKZx9c1sKODqgjfpK3QS3FTh9dM8Q98vP11ffCFX3z5_vfh4RbxQZiFqYGOngdKgQ0vWS85N4OBYx4Phph8GUL30on3BIMFzGHvjHIeWVg-jCeIMvd989yXfr1AXO8fqYZpcgrxW25RCa22E-j9KtZBaacYb-u4v9C6vJbUgR4obZWRnGsU3ypdca4Fg9yXOrhwso_ZYp93qtK1O-1infWiit0_W6zDD-Fvyq78GiA2obZVuoPx5-x-2PwE1W6x9</recordid><startdate>20241201</startdate><enddate>20241201</enddate><creator>El makawy, Aida I.</creator><creator>Mabrouk, Dalia M.</creator><creator>Ibrahim, Faten M.</creator><creator>Abdel-Aziem, Sekena H.</creator><creator>EL-Kader, Heba A.M. Abd</creator><creator>Youssef, Dalia A.</creator><creator>Sharaf, Hafiza A.</creator><creator>Mohammed, Shaimaa E.</creator><general>Springer Netherlands</general><general>Springer Nature B.V</general><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>7TK</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><orcidid>https://orcid.org/0000-0001-8335-5381</orcidid></search><sort><creationdate>20241201</creationdate><title>Formulation of quinoa oil-alginate loaded nanoemulsion and its anticancer efficacy as a therapy for chemically induced breast cancer</title><author>El makawy, Aida I. ; Mabrouk, Dalia M. ; Ibrahim, Faten M. ; Abdel-Aziem, Sekena H. ; EL-Kader, Heba A.M. Abd ; Youssef, Dalia A. ; Sharaf, Hafiza A. ; Mohammed, Shaimaa E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c359t-5b1d76e00f6f30184229f2ea172f9298bbe584c3157b4ec2ed89aa2e3886bd9f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>acute oral toxicity</topic><topic>Alginates - chemistry</topic><topic>Alginates - pharmacology</topic><topic>Alginic acid</topic><topic>Animal Anatomy</topic><topic>Animal Biochemistry</topic><topic>Animals</topic><topic>Anthracene</topic><topic>anthracenes</topic><topic>Anti-oncogenes</topic><topic>antineoplastic activity</topic><topic>Antineoplastic Agents - pharmacology</topic><topic>Antioxidants - pharmacology</topic><topic>Antitumor activity</topic><topic>Biomedical and Life Sciences</topic><topic>blood serum</topic><topic>Breast cancer</topic><topic>breast neoplasms</topic><topic>Breast Neoplasms - drug therapy</topic><topic>Breast Neoplasms - pathology</topic><topic>breasts</topic><topic>Chenopodium quinoa</topic><topic>Chenopodium quinoa - chemistry</topic><topic>Colorectal cancer</topic><topic>Colorectal carcinoma</topic><topic>colorectal neoplasms</topic><topic>drug therapy</topic><topic>Emulsions</topic><topic>Female</topic><topic>Free radicals</topic><topic>Gas chromatography</topic><topic>gas chromatography-mass spectrometry</topic><topic>Gene expression</topic><topic>Histology</topic><topic>histopathology</topic><topic>Humans</topic><topic>Life Sciences</topic><topic>Mass spectroscopy</topic><topic>Morphology</topic><topic>Nanoemulsions</topic><topic>Nanoparticles - chemistry</topic><topic>neoplasm progression</topic><topic>oils</topic><topic>Oils & fats</topic><topic>Original Article</topic><topic>Oxidative stress</topic><topic>Oxidative Stress - drug effects</topic><topic>phytochemicals</topic><topic>Plant Oils - chemistry</topic><topic>Plant Oils - pharmacology</topic><topic>Quinoa</topic><topic>Rats</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>Seeds - chemistry</topic><topic>Sodium alginate</topic><topic>Toxicity</topic><topic>tumor suppressor genes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>El makawy, Aida I.</creatorcontrib><creatorcontrib>Mabrouk, Dalia M.</creatorcontrib><creatorcontrib>Ibrahim, Faten M.</creatorcontrib><creatorcontrib>Abdel-Aziem, Sekena H.</creatorcontrib><creatorcontrib>EL-Kader, Heba A.M. Abd</creatorcontrib><creatorcontrib>Youssef, Dalia A.</creatorcontrib><creatorcontrib>Sharaf, Hafiza A.</creatorcontrib><creatorcontrib>Mohammed, Shaimaa E.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Molecular biology reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>El makawy, Aida I.</au><au>Mabrouk, Dalia M.</au><au>Ibrahim, Faten M.</au><au>Abdel-Aziem, Sekena H.</au><au>EL-Kader, Heba A.M. Abd</au><au>Youssef, Dalia A.</au><au>Sharaf, Hafiza A.</au><au>Mohammed, Shaimaa E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Formulation of quinoa oil-alginate loaded nanoemulsion and its anticancer efficacy as a therapy for chemically induced breast cancer</atitle><jtitle>Molecular biology reports</jtitle><stitle>Mol Biol Rep</stitle><addtitle>Mol Biol Rep</addtitle><date>2024-12-01</date><risdate>2024</risdate><volume>51</volume><issue>1</issue><spage>705</spage><epage>705</epage><pages>705-705</pages><artnum>705</artnum><issn>0301-4851</issn><issn>1573-4978</issn><eissn>1573-4978</eissn><abstract>Background
Quinoa seeds (
Chenopodium quinoa
Willd.) have gained interest due to their naturally occurring phytochemicals and antioxidants. They possess potent anticancer properties against human colorectal cancer. Methods and Results: Fatty acids in quinoa oil were studied using gas chromatography-mass spectrometry. Rats were used to test the acute oral toxicity of the nanoemulsion loaded with sodium alginate. The DPPH radical scavenging method was employed to assess the nanoemulsion’s ability to scavenge free radicals. It was examined the in vivo anticancer potential of quinoa oil nanoemulsion on rats with breast cancer induced by 7, 12-dimethylbenz (a) anthracene (DMBA). DMBA-breast cancer models received daily quinoa oil nanoemulsions for 30 days. The anticancer effect of the nanoemulsion was assessed by measuring ROS, protein carbonyl, gene expression of anti-oncogenes, and histopathological analysis. Supplying quinoa oil nanoemulsion significantly reduced the increase in serum ROS and PC levels induced in breast cancer tissue. The expression levels of antioncogenes in breast cancer tissue were decreased by the quinoa oil nanoemulsion. Nanoemulsions also improved the cellular morphology of breast tumors. Conclusion: The study results indicate that quinoa oil nanoemulsion has anticancer activity against breast cancer, effectively modulating oxidative stress markers, anti-oncogene expressions, and tissue architecture. It can be inferred from the results that quinoa oil nanoemulsion is a chemoprotective medication that may hinder breast cancer progression in rats.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>38824214</pmid><doi>10.1007/s11033-024-09619-x</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-8335-5381</orcidid></addata></record> |
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subjects | acute oral toxicity Alginates - chemistry Alginates - pharmacology Alginic acid Animal Anatomy Animal Biochemistry Animals Anthracene anthracenes Anti-oncogenes antineoplastic activity Antineoplastic Agents - pharmacology Antioxidants - pharmacology Antitumor activity Biomedical and Life Sciences blood serum Breast cancer breast neoplasms Breast Neoplasms - drug therapy Breast Neoplasms - pathology breasts Chenopodium quinoa Chenopodium quinoa - chemistry Colorectal cancer Colorectal carcinoma colorectal neoplasms drug therapy Emulsions Female Free radicals Gas chromatography gas chromatography-mass spectrometry Gene expression Histology histopathology Humans Life Sciences Mass spectroscopy Morphology Nanoemulsions Nanoparticles - chemistry neoplasm progression oils Oils & fats Original Article Oxidative stress Oxidative Stress - drug effects phytochemicals Plant Oils - chemistry Plant Oils - pharmacology Quinoa Rats Reactive Oxygen Species - metabolism Seeds - chemistry Sodium alginate Toxicity tumor suppressor genes |
title | Formulation of quinoa oil-alginate loaded nanoemulsion and its anticancer efficacy as a therapy for chemically induced breast cancer |
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