The cooperation of the tumor suppressor gene Dlc1 and the oncogene Kras in tumorigenesis

dc.contributor.authorBuse, Cordula
dc.contributor.examiningcommitteeMai, Sabine (Biochemistry and Medical Genetics) Merz, David (Biochemistry and Medical Genetics) Halayko, Andrew (Physiology)en_US
dc.contributor.supervisorMowat, Michael (Biochemistry and Medical Genetics)en_US
dc.date.accessioned2012-10-25T13:12:07Z
dc.date.available2012-10-25T13:12:07Z
dc.date.issued2012-10-25
dc.degree.disciplineBiochemistry and Medical Geneticsen_US
dc.degree.levelMaster of Science (M.Sc.)en_US
dc.description.abstractThis thesis investigated the cooperation of the Kras2 oncogene with the tumor suppressor gene Dlc1 in lung tumor development. Dlc1 is a negative regulator of RhoGTPase proteins, which are mainly involved in the regulation of the actin cytoskeleton and cell migration. We hypothesized that loss of Dlc1 expression leads to more aggressive tumors, which should also result in increased incidence of metastasis. All experiments were performed in mice containing a heterozygous oncogenic Kras allele and a heterozygous gene trapped Dlc1 allele (KD) and in mice only carrying the oncogenic Kras allele (K+). Throughout all experiments we have consistently found no significant differences between the two groups in terms of tumor burden (tumor numbers, sizes and areas), metastases or methylation patterns. These results suggest that heterozygous downregulation of Dlc1 is not enough to increase tumor formation and metastasis development in the Kras lung tumors.en_US
dc.description.noteFebruary 2013en_US
dc.identifier.urihttp://hdl.handle.net/1993/9675
dc.language.isoengen_US
dc.rightsopen accessen_US
dc.subjectlung canceren_US
dc.subjectmouse modelen_US
dc.subjectKrasen_US
dc.subjectDlc1en_US
dc.subjectoncogeneen_US
dc.subjecttumor suppressoren_US
dc.titleThe cooperation of the tumor suppressor gene Dlc1 and the oncogene Kras in tumorigenesisen_US
dc.typemaster thesisen_US
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