Abstract

The human zinc finger (C2H2-type) protein ZNF750 is a transcription factor regulated by p63 that plays a critical role in epithelial tissues homoeostasis, as well as being involved in the pathogenesis of cancer. Indeed, missense mutations, truncation and genomic deletion have been found in oesophageal squamous cell carcinoma. In keeping, we showed that ZNF750 negatively regulates cell migration and invasion in breast cancer cells; in particular, ZNF750 binds and recruits KDM1A and HDAC1 on the LAMB3 and CTNNAL1 promoters. This interaction, in turn, represses the transcription of LAMB3 and CTNNAL1 genes, which are involved in cell migration and invasion. Given that ZNF750 is emerging as a crucial transcription factor that acts as tumour suppressor gene, here, we show that ZNF750 represses the expression of the small GTPase, Ras-related C3 botulinum toxin substrate 1 (RAC1) in breast cancer cell lines, by directly binding its promoter region. In keeping with ZNF750 controlling RAC1 expression, we found an inverse correlation between ZNF750 and RAC1 in human breast cancer datasets. More importantly, we found a significant upregulation of RAC1 in human breast cancer datasets and we identified a direct correlation between RAC1 expression and the survival rate of breast cancer patient. Overall, our findings provide a novel molecular mechanism by which ZNF750 acts as tumour suppressor gene. Hence, we report a potential clinical relevance of ZNF750/RAC1 axis in breast cancer.

Highlights

  • ZNF750 is a zinc finger transcription factor that plays an important role in controlling the homoeostasis of epithelial tissue[1,2]

  • related C3 botulinum toxin substrate 1 (RAC1) is upregulated in breast cancer cells and its expression is controlled by ZNF750

  • We have recently found that RAC1 was upregulated after ZNF750 depletion in breast cancer cell lines

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Summary

Introduction

ZNF750 is a zinc finger transcription factor that plays an important role in controlling the homoeostasis of epithelial tissue[1,2]. ZNF750 deregulation results in neoplastic transformation[3]. ZNF750 consists of an atypical C2H2 zinc finger motif in the N-terminal domain, which is required for ZNF750 transcriptional function. Two highly conserved PLNLS motifs, that are required for protein–protein interaction, are present in the C-terminal domain[4]. ZNF750 regulates epidermal differentiation by activating differentiation gene expression cooperatively with KLF4 and by inhibiting the expression of progenitor genes in association with KDM1A. ZNF750 has been described as a tumour suppressor protein in squamous cell

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