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Journal of Korean Medical Science ; : e100-2019.
Article in English | WPRIM | ID: wpr-764935

ABSTRACT

BACKGROUND: Increased expression of MDR1 gene is one of the major mechanisms responsible for multidrug resistance in cancer cells. Two alternative promoters, upstream and downstream, are responsible for transcription of MDR1 gene in the human. However, the molecular mechanism regarding the transactivation of MDR1 upstream promoter (USP) has not been determined. METHODS: Dual-luciferase reporter gene assays were used to assess the effect of Nkx-2.5 on MDR1 USP activity using reporter plasmids for human MDR1 USP and its mutants. MDR1 mRNA level was examined by quantitative real-time PCR. The direct binding of Nkx-2.5 to the USP of MDR1 was evaluated by promoter enzyme immunoassays and chromatin immunoprecipitation assays.


Subject(s)
Humans , Breast Neoplasms , Breast , Chromatin Immunoprecipitation , Drug Resistance, Multiple , Genes, Reporter , Immunoassay , Immunoenzyme Techniques , Phenotype , Plasmids , Real-Time Polymerase Chain Reaction , RNA, Messenger , Transcriptional Activation
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