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dc.contributor.authorConstantinou, Andreas I.en
dc.contributor.authorMehta, R. G.en
dc.contributor.authorVaughan, A.en
dc.creatorConstantinou, Andreas I.en
dc.creatorMehta, R. G.en
dc.creatorVaughan, A.en
dc.date.accessioned2019-11-04T12:50:23Z
dc.date.available2019-11-04T12:50:23Z
dc.date.issued1996
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/53000
dc.description.abstractSoy-based diets, rich in the isoflavones genistein and daidzein, are thought to protect against breast and prostate cancer. Soy-based diets, rich in the isoflavones genistein and daidzein, are thought to protect against breast and prostate cancer. We used the N-methyl-N-nitrosourea (MNU)-induced mammary carcinogenesis animal model to test the effectiveness of these two isoflavones as chemopreventive agents. Each isoflavone was injected daily into 35-day-old rats for six months while we monitored the animals' body weight and mammary tumor appearance. Genistein was effective in reducing tumor multiplicity, but it reduced tumor incidence only marginally. Daidzein was less effective in reducing both tumor incidence and multiplicity. To investigate genistein's mechanism of action we determined the topoisomerase II (topo II) activity and detected the phosphotyrosine-containing peptides in the extracts of mammary tissues isolated from control and isoflavone-treated animals. Mammary tumors contained over 60-fold higher topo II enzymatic activity than the mammary glands. Similarly, more tyrosine phosphopeptides were detectable in mammary tumors than in mammary glands. Tissue samples from genistein treated animals contained similar topo II and protein tyrosine kinase (PTK) activities as the control group. These data suggest that mammary tumorigenesis is accompanied by an extensive increase in topo II and PTK activities. The mechanism of chemoprevention by genistein, however, is independent of topo II or PTK inhibition.en
dc.sourceAnticancer Researchen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-0030507470&partnerID=40&md5=41454b5761116f344ddb083d130ba9db
dc.subjectarticleen
dc.subjectAntineoplastic Agentsen
dc.subjectcontrolled studyen
dc.subjectfemaleen
dc.subjectpriority journalen
dc.subjectdrug efficacyen
dc.subjectcancer incidenceen
dc.subjectChemopreventionen
dc.subjectnonhumanen
dc.subjectdrug mechanismen
dc.subjectAnimalsen
dc.subjectanimal experimenten
dc.subjectanimal modelen
dc.subjectanimal tissueen
dc.subjectbreast carcinogenesisen
dc.subjectenzyme activityen
dc.subjectbody weighten
dc.subjectbreast tumoren
dc.subjectchemoprophylaxisen
dc.subjectDNA Topoisomerases, Type IIen
dc.subjectPhosphorylationen
dc.subjectdaidzeinen
dc.subjectgenisteinen
dc.subjectsoybeanen
dc.subjectisoflavone derivativeen
dc.subjectIsoflavonesen
dc.subjectMammary Glands, Animalen
dc.subjectraten
dc.subjectRatsen
dc.subjectRats, Sprague-Dawleyen
dc.subjectCarcinogenesisen
dc.subjectDrug Screening Assays, Antitumoren
dc.subjectTopoisomerase IIen
dc.subjectdna topoisomerase (atp hydrolysing)en
dc.subjectMammary Neoplasms, Experimentalen
dc.subjectSoybeansen
dc.subjectCarcinogensen
dc.subjectintraperitoneal drug administrationen
dc.subjectmethylnitrosoureaen
dc.subjectProtein tyrosine kinaseen
dc.subjectProtein-Tyrosine Kinasesen
dc.titleInhibition of N-methyl-N-nitrosourea-induced mammary tumors in rats by the soybean isoflavonesen
dc.typeinfo:eu-repo/semantics/article
dc.description.volume16
dc.description.startingpage3293
dc.description.endingpage3298
dc.author.facultyΣχολή Θετικών και Εφαρμοσμένων Επιστημών / Faculty of Pure and Applied Sciences
dc.author.departmentΤμήμα Βιολογικών Επιστημών / Department of Biological Sciences
dc.type.uhtypeArticleen
dc.description.notes<p>Manufacturers: indofine, United Statesen
dc.description.notesCited By :115</p>en
dc.source.abbreviationAnticancer Res.en
dc.contributor.orcidConstantinou, Andreas I. [0000-0003-0365-1821]
dc.gnosis.orcid0000-0003-0365-1821


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