4.4 Article

Differentiation-related zinc finger protein 750 suppresses cell growth in esophageal squamous cell carcinoma

期刊

ONCOLOGY LETTERS
卷 22, 期 1, 页码 -

出版社

SPANDIDOS PUBL LTD
DOI: 10.3892/ol.2021.12774

关键词

esophageal squamous cell carcinoma; zinc finger protein 750; keratinocyte differentiation; squamous cell carcinoma; tumor suppressor gene

类别

资金

  1. Research Grants Council Collaborative Research Fund [106150246]
  2. Theme-based Research Scheme [T12-701/17-R]
  3. Asian Cancer Research Fund

向作者/读者索取更多资源

This study investigated the role of ZNF750 in inducing cell differentiation and suppressing tumor growth in esophageal squamous cell carcinoma (ESCC). The results revealed a functional link between ZNF750's ability to induce cell differentiation through to terminal differentiation and its function as a growth suppressor in ESCC.
Esophageal squamous cell carcinoma (ESCC) is a deadly squamous cell carcinoma (SCC) of the esophagus. Development of SCCs is associated with the deregulation of the squamous cell lineage program and/or keratinocyte terminal differentiation by genomic and genetic aberrations; thus, these processes must be tightly controlled to maintain normal squamous cell development. Zinc finger protein 750 (ZNF750) is a gene involved in keratinocyte terminal differentiation and is frequently mutated and putatively silenced in ESCC, which implicates its function as a potential differentiation-related suppressor of ESCC. The present study aimed to elucidate the relationship between ZNF750 function to induce keratinocyte differentiation and tumor suppression in ESCC. The results demonstrated that chemical manipulation of esophageal keratinocyte differentiation in mouse normal esophageal epithelial organoids (mNEEO) implicated the involvement of the mouse homologue of ZNF750, Zfp750, in keratinocyte differentiation in premalignant cells. Bioinformatics analyses of data from high ZNF750-expressing ESCC tumors obtained from public databases and ZNF750-overexpressing ESCC cells compared with low ZNF750-expressing ESCC tumors and GFP-expressing ESCC cells, respectively, revealed enrichment of keratinocyte differentiation-related gene sets in these samples. Finally, the induction through to terminal differentiation of the keratinocyte by all-trans retinoic acid on parental ESCC cell lines led to the upregulation of the terminal differentiation marker Involucrin and a decrease in cell viability similar to that observed in ZNF750-overexpressing ESCC cells. The results of the present study demonstrated a functional link between the ability of ZNF750 to induce cell differentiation through to terminal differentiation and its function as a growth suppressor in ESCC. This study provides improved understanding of the role of ZNF750, a frequently mutated differentiation-related gene in ESCC, and its effects in ESCC pathogenesis.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.4
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据