Abstract

Zinc finger protein 91 (ZFP91) has been reported to be involved in various biological processes. However, the clinical significance and biological role of ZFP91 in colon cancer remains unknown. Here, we show that ZFP91 expression is upregulated in patients with colon cancer. We found that ZFP91 upregulated HIF-1α at the levels of promoter and protein in colon cancer cells. Using chromatin immunoprecipitation, electrophoretic mobility shift assay and luciferase reporter gene assay, we found that NF-κB/p65 is required for the binding of ZFP91 to the HIF-1α promoter at −197/−188 base pairs and for the transcriptional activation of HIF-1α gene mediated by ZFP91. Flow cytometry, 5-ethynyl-2′-deoxyuridine (EdU) incorporation and tumor xenograft assay demonstrated that ZFP91 enhanced cell proliferation of colon cancer through upregulating HIF-1α in vitro and in vivo. Furthermore, ZFP91 is positively associated with HIF-1α in human colon cancer. Thus, we concluded that ZFP91 activates transcriptional coregulatory protein HIF-1α through transcription factor NF-κB/p65 in the promotion of proliferation and tumorigenesis in colon cancer cell. ZFP91 may serve as a driver gene to activate HIF-1α transcription in the development of cancer.

Highlights

  • Zinc finger protein (ZFP91), a conserved 63.5kDa nuclear protein with structural motifs characteristic of transcription factor, contain five zinc-finer domains, one leucine-zipper pattern, one coiled-coil structure, and several nuclear localization signals [1]

  • Zinc finger protein 91 (ZFP91) is positively associated with HIF-1α in human colon cancer

  • The human colon cancer specimens exhibited a robust expression of ZFP91 and HIF-1α compared with adjacent tissues (Figure 1A)

Read more

Summary

Introduction

Zinc finger protein (ZFP91), a conserved 63.5kDa nuclear protein with structural motifs characteristic of transcription factor, contain five zinc-finer domains, one leucine-zipper pattern, one coiled-coil structure, and several nuclear localization signals [1]. It has been reported that ZFP91 interacts with ARF tumor suppressor (cyclin-dependent kinase inhibitor 2A), which is known for its induction of p53-dependent cell death or growth arrest in response to activated oncogenes [2]. ZFP91 plays a critical role in acute myelogenous leukemia and prostate pathology [3, 4]. Our previous study indicated that ZFP91 is an atypical E3 ligase activating NF-κBinducing kinase (NIK) via Lys63-linked ubiquitination in the noncanonical NF-κB signaling pathway [5, 6]. HIF-1 is a heterodimeric transcription factor composed of α and β subunits [8]

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call