Kruppel-family zinc finger proteins as emerging epigenetic biomarkers in head and neck squamous cell carcinoma

Author:

Pearson Patrick1,Smith Kendra12,Sood Nilita2,Chia Elizabeth12,Follett Alicia1,Prystowsky Michael B.3,Kirby Simon4,Belbin Thomas J.123ORCID

Affiliation:

1. Division of Biomedical Sciences, Faculty of Medicine, Memorial University of Newfoundland, A1B 3V6, St. John's, NL, Canada

2. Discipline of Oncology, Faculty of Medicine, Memorial University of Newfoundland, A1B 3V6, St. John's, NL, Canada

3. Department of Pathology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, 10461, Bronx, NY, USA

4. Discipline of Laboratory Medicine, Faculty of Medicine, Memorial University of Newfoundland, A1B 3V6, St. John's, NL, Canada

Abstract

Background Krüppel-type zinc finger protein genes located on chromosome 19q13 are aberrantly hypermethylated with high frequency in all anatomic sub-sites of head and neck cancers as well as other epithelial tumours resulting in decreased expression. Methods We examined prognostic significance of ZNF154 and ZNF132 expression and DNA methylation in independent patient cohort of about 500 head and neck cancer patients in the Cancer Genome Atlas (TCGA). We also overexpressed these genes in HEK-293 cells, as well as the oral cancer cell line UM-SCC-1. Results In 20 patients from the TCGA cohort of HNSCC patients where ZNF154 and ZNF132 DNA methylation and RNA expression could be compared in tumor and adjacent normal tissue, there was increased DNA methylation and decreased expression of both ZNF154 and ZNF132 in primary tumours. Low ZNF154 and low ZNF132 expression were associated with shorter overall survival in both head and neck squamous cell carcinoma (HNSCC) and lung adenocarcinoma (LUAC patients). While expression of these proteins in HEK-293 cells produced full-length protein, only truncated copies could be expressed in head and neck cancer cells (UM-SCC-1). The truncated version of ZNF154 protein increased doubling time and reduced cell migration in UM-SCC-1 cancer cells. Conclusions Both ZNF132 and ZNF154 represent novel clinically significant biomarkers in head and neck cancer with potential tumour suppressive properties. Future studies will address the underlying molecular mechanisms by which ZNF154 expression in HNSCC contributes to the control of cell growth and migration. Graphical Abstract

Funder

Beatrice Hunter Cancer Research Institute

Publisher

SAGE Publications

Subject

Otorhinolaryngology,Surgery

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