Division of Biomedical Sciences, Faculty of Medicine, Memorial University of Newfoundland, St. John's, NL, A1B 3V6, Canada.
Discipline of Oncology, Faculty of Medicine, Memorial University of Newfoundland, St. John's, NL, A1B 3V6, Canada.
J Otolaryngol Head Neck Surg. 2023 May 30;52(1):41. doi: 10.1186/s40463-023-00640-x.
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.
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.
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.
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.
位于 19 号染色体上的 Krüppel 型锌指蛋白基因在头颈部癌症以及其他上皮肿瘤的所有解剖部位都高频出现异常高甲基化,导致表达降低。
我们在癌症基因组图谱(TCGA)中约 500 名头颈部癌症患者的独立患者队列中检查了 ZNF154 和 ZNF132 表达和 DNA 甲基化的预后意义。我们还在 HEK-293 细胞以及口腔癌细胞系 UM-SCC-1 中过表达了这些基因。
在 TCGA 队列中 20 名头颈部癌症患者中,可比较肿瘤和相邻正常组织中的 ZNF154 和 ZNF132 DNA 甲基化和 RNA 表达,原发肿瘤中 ZNF154 和 ZNF132 的 DNA 甲基化增加且表达降低。ZNF154 和 ZNF132 低表达与头颈部鳞状细胞癌(HNSCC)和肺腺癌(LUAC 患者)患者的总生存期较短相关。虽然这些蛋白在 HEK-293 细胞中的表达产生全长蛋白,但仅在头颈部癌症细胞(UM-SCC-1)中可表达截断拷贝。ZNF154 蛋白的截断形式增加了 UM-SCC-1 癌细胞的倍增时间并减少了细胞迁移。
ZNF132 和 ZNF154 均代表头颈部癌症中具有潜在肿瘤抑制特性的新型临床显著生物标志物。未来的研究将解决 ZNF154 在 HNSCC 中表达如何控制细胞生长和迁移的潜在分子机制。