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ABSTRACT: Objective
The aim of this study was to investigate the role of KIF26A in breast cancer.Method
qRT-PCR and immunohistochemistry were conducted to explore KIF26A expression and functional contribution to breast cancer development. MTS, EDU, colony formation assays, and flow cytometry analysis were conducted to assess cell proliferation characteristics and cell cycle progression. A series of 5'-flanking region deletion plasmids and mutating the binding site, with the luciferase reporter assay, were used to identify the core promotor region of KIF26A. The prediction by software and construction of the transcriptional factor plasmids were used to identify the transcriptional factor. Chromatin immunoprecipitation assay could demonstrate transcriptional factor directly binding to
SUBMITTER: Xu J
PROVIDER: S-EPMC7832431 | biostudies-literature | 2020
REPOSITORIES: biostudies-literature