12-O-Tetradecanoylphorbol-13-acetate Promotes Breast Cancer Cell Motility by Increasing S100A14 Level in a Kruppel-like Transcription Factor 4 (KLF4)-dependent Manner

• Published in: The Journal of biological chemistry 2014-03, Vol.289 (13), p.9089-9099
• Main Authors: He, Huan, Li, Sheng, Chen, Hongyan, Li, Lin, Xu, Chengshan, Ding, Fang, Zhan, Yun, Ma, Jianlin, Zhang, Shuguang, Shi, Yaoting, Qu, Chunfeng, Liu, Zhihua
• Format: Article
• Language: English
• Subjects: Animals; Base Sequence; Binding Sites; Breast Cancer; Breast Neoplasms - pathology; Calcium-Binding Proteins - deficiency; Calcium-Binding Proteins - genetics; Calcium-Binding Proteins - metabolism; Cell Biology; Cell Line, Tumor; Cell Motility; Cell Movement - drug effects; Dose-Response Relationship, Drug; Gene Expression Regulation, Neoplastic - drug effects; Gene Regulation; Gene Silencing; Humans; Kruppel-like Factor (KLF); Kruppel-Like Transcription Factors - deficiency; Kruppel-Like Transcription Factors - genetics; Kruppel-Like Transcription Factors - metabolism; Mice; RNA, Messenger - genetics; RNA, Messenger - metabolism; S100 Proteins; Tetradecanoylphorbol Acetate - pharmacology; Time Factors; TPA
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M113.534271

The S100 protein family represents the largest subgroup of calcium binding EF-hand type proteins. These proteins have been reported to be involved in a wide range of biological functions that are related to normal cell development and tumorigenesis. S100A14 is a recently identified member of the S100 protein family and differentially expressed in a number of different human malignancies. However, the transcriptional regulation of S100A14 and its role in breast cancer needs to be further investigated. Here, we determined that 12-O-tetradecanoylphorbol-13-acetate (TPA) up-regulated the expression of KLF4 and facilitated its binding directly to two conserved GC-rich DNA segments within the S100A14 promoter, which is essential for the transactivation of KLF4 induced S100A14 expression. Furthermore, stable silencing of KLF4 significantly suppressed breast cancer cell migration induced by TPA. Collectively, these results offer insights into the fact that TPA provokes cell motility through regulating the expression and function of S100A14 in a KLF4-dependent manner. Background: The transcriptional regulation of S100A14 and its underlying mechanism have not been fully elucidated. Results: The activation of S100A14 promoter by KLF4 mediates its up-regulation upon TPA stimulation. Conclusion: S100A14 partly mediates TPA-induced cell motility in a KLF4-dependent manner. Significance: KLF4 plays a significant and previously unrecognized role in regulation of S100A14.