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Article: Differentiation‑related zinc finger protein 750 suppresses cell growth in esophageal squamous cell carcinoma

TitleDifferentiation‑related zinc finger protein 750 suppresses cell growth in esophageal squamous cell carcinoma
Authors
KeywordsEsophageal squamous cell carcinoma
Keratinocyte differentiation
Squamous cell carcinoma
Tumor suppressor gene
Zinc finger protein 750
Issue Date2021
PublisherSpandidos Publications. The Journal's web site is located at http://www.spandidos-publications.com/ol
Citation
Oncology Letters, 2021, v. 22 n. 1, p. article no. 513 How to Cite?
AbstractEsophageal 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.
Persistent Identifierhttp://hdl.handle.net/10722/301262
ISSN
2021 Impact Factor: 3.111
2020 SCImago Journal Rankings: 0.766
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorChoi, SSA-
dc.contributor.authorKo, JMY-
dc.contributor.authorYu, VZ-
dc.contributor.authorNing, L-
dc.contributor.authorLung, ML-
dc.date.accessioned2021-07-27T08:08:31Z-
dc.date.available2021-07-27T08:08:31Z-
dc.date.issued2021-
dc.identifier.citationOncology Letters, 2021, v. 22 n. 1, p. article no. 513-
dc.identifier.issn1792-1074-
dc.identifier.urihttp://hdl.handle.net/10722/301262-
dc.description.abstractEsophageal 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.-
dc.languageeng-
dc.publisherSpandidos Publications. The Journal's web site is located at http://www.spandidos-publications.com/ol-
dc.relation.ispartofOncology Letters-
dc.subjectEsophageal squamous cell carcinoma-
dc.subjectKeratinocyte differentiation-
dc.subjectSquamous cell carcinoma-
dc.subjectTumor suppressor gene-
dc.subjectZinc finger protein 750-
dc.titleDifferentiation‑related zinc finger protein 750 suppresses cell growth in esophageal squamous cell carcinoma-
dc.typeArticle-
dc.identifier.emailKo, JMY: joko@hku.hk-
dc.identifier.emailYu, VZ: zvyu@hku.hk-
dc.identifier.emailLung, ML: mlilung@hku.hk-
dc.identifier.authorityKo, JMY=rp02011-
dc.identifier.authorityYu, VZ=rp02756-
dc.identifier.authorityLung, ML=rp00300-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.3892/ol.2021.12774-
dc.identifier.scopuseid_2-s2.0-85105686549-
dc.identifier.hkuros323395-
dc.identifier.volume22-
dc.identifier.issue1-
dc.identifier.spagearticle no. 513-
dc.identifier.epagearticle no. 513-
dc.identifier.isiWOS:000649706800001-
dc.publisher.placeGreece-

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