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The azoxymethane plus dextran sulfate sodium-induced mouse colon cancer model for the study of dietary chemoprevention of inflammation-associated carcinogenesis

DC Field Value Language
dc.contributor.authorLee, Ha-Na-
dc.contributor.authorYum, Hye-Won-
dc.contributor.authorSurh, Young-Joon-
dc.date.accessioned2021-01-31T10:19:30Z-
dc.date.available2021-01-31T10:19:30Z-
dc.date.created2017-11-15-
dc.date.issued2014-
dc.identifier.citationMethods in Pharmacology and Toxicology, pp.155-172-
dc.identifier.issn1557-2153-
dc.identifier.other5746-
dc.identifier.urihttps://hdl.handle.net/10371/172826-
dc.description.abstractThe azoxymethane (AOM) plus dextran sulfate sodium (DSS)-induced mouse colon carcinogenesis model is a fascinating tool for investigating the pathogenesis and chemoprevention of colitis-associated colorectal cancer. In this two-stage mouse colon cancer model, tumorigenesis is initiated by a single intraperitoneal administration of the carcinogen AOM and promoted by DSS-induced inflammation. The successful induction of AOM plus DSS-induced colorectal cancer relies on several critical factors, such as the molecular weight and the dosage of DSS, the strain, age, and sex of animals, and other experimental conditions. Here, we provide the optimized protocol for effective induction of colon tumors in mice by treatment with AOM plus DSS. Inflammation-induced colon carcinogenesis is accompanied by a series of histopathological and molecular changes. In this chapter, we also describe the step-by-step protocols for macroscopic examination, hematoxylin and eosin (H & E) staining, immunohistochemical analysis, immunoblot analysis, and the electrophoretic mobility shift assay, all of which are used for investigating the inflammation-associated colon carcinogenesis and the chemopreventive effect of dietary phytochemicals. © 2014 Springer Science+Business Media New York.-
dc.language영어-
dc.publisherHumana Press, Inc.-
dc.titleThe azoxymethane plus dextran sulfate sodium-induced mouse colon cancer model for the study of dietary chemoprevention of inflammation-associated carcinogenesis-
dc.typeArticle-
dc.contributor.AlternativeAuthor서영준-
dc.citation.journaltitleMethods in Pharmacology and Toxicology-
dc.identifier.scopusid2-s2.0-84891786193-
dc.citation.endpage172-
dc.citation.startpage155-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorSurh, Young-Joon-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusazoxymethane-
dc.subject.keywordPlusdextran sulfate-
dc.subject.keywordPlusDNA-
dc.subject.keywordPlustumor protein-
dc.subject.keywordPlusanimal experiment-
dc.subject.keywordPlusanimal model-
dc.subject.keywordPlusanimal tissue-
dc.subject.keywordPlusarticle-
dc.subject.keywordPlusbinding affinity-
dc.subject.keywordPlusbinding site-
dc.subject.keywordPluscancer prevention-
dc.subject.keywordPluscolitis-
dc.subject.keywordPluscolon cancer-
dc.subject.keywordPluscolon carcinogenesis-
dc.subject.keywordPluscontrolled study-
dc.subject.keywordPlusdietary intake-
dc.subject.keywordPlusdisease activity-
dc.subject.keywordPlusdisease association-
dc.subject.keywordPlusdisease severity-
dc.subject.keywordPlusfemale-
dc.subject.keywordPlusgel mobility shift assay-
dc.subject.keywordPlushistopathology-
dc.subject.keywordPlusimmunoblotting-
dc.subject.keywordPlusimmunohistochemistry-
dc.subject.keywordPlusmale-
dc.subject.keywordPlusmolecular dynamics-
dc.subject.keywordPlusmolecular pathology-
dc.subject.keywordPlusmouse-
dc.subject.keywordPlusnonhuman-
dc.subject.keywordPlusphytochemistry-
dc.subject.keywordPluspriority journal-
dc.subject.keywordPlusprotein determination-
dc.subject.keywordPlusprotein DNA binding-
dc.subject.keywordPlusprotein expression-
dc.subject.keywordPlusprotein function-
dc.subject.keywordAuthorAOM plus DSS-induced colon carcinogenesis-
dc.subject.keywordAuthorDSS-induced colitis-
dc.subject.keywordAuthorEMSA-
dc.subject.keywordAuthorH &-
dc.subject.keywordAuthorE staining-
dc.subject.keywordAuthorIHC analysis-
dc.subject.keywordAuthorImmunoblot analysis-
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  • College of Pharmacy
  • Department of Pharmacy
Research Area Agricultural Sciences

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