Cargando…
Identification of ZNF704 as a Novel Oncogene and an Independent Prognostic Marker in Chondrosarcoma
PURPOSE: The transcription factor zinc finger protein 704 (ZNF704) is implicated in tumorigenesis. However, the underlying role of ZNF704 in the pathogenesis of chondrosarcoma remains not well delineated. This study investigates the expression level, prognostic significance and potential biological...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8232878/ https://www.ncbi.nlm.nih.gov/pubmed/34188544 http://dx.doi.org/10.2147/CMAR.S313229 |
_version_ | 1783713730490531840 |
---|---|
author | Chen, Changbao Zhou, Hua Zhang, Xiaolin Liu, Zhongjun Ma, Xinlong |
author_facet | Chen, Changbao Zhou, Hua Zhang, Xiaolin Liu, Zhongjun Ma, Xinlong |
author_sort | Chen, Changbao |
collection | PubMed |
description | PURPOSE: The transcription factor zinc finger protein 704 (ZNF704) is implicated in tumorigenesis. However, the underlying role of ZNF704 in the pathogenesis of chondrosarcoma remains not well delineated. This study investigates the expression level, prognostic significance and potential biological function of ZNF704 in human chondrosarcoma. MATERIALS AND METHODS: The mRNA and protein levels of ZNF704 in fresh chondrosarcomas and the paired adjacent non-tumor tissues were evaluated using real-time PCR and immunoblotting, respectively. The protein expression of ZNF704 in chondrosarcoma specimens was detected by immunohistochemistry, and the associations among its expression level, clinicopathological characteristics and prognosis were further investigated. Cell viability, colony formation and apoptosis assay were determined in chondrosarcoma cells and a xenograft model with ZNF704 knockdown. RESULTS: The expression levels of ZNF704 mRNA and protein in chondrosarcoma tissues were significantly higher than those in the paired adjacent non-tumor tissues and benign cartilage tumors. Clinicopathological analysis revealed that ZNF704 was expressed at higher levels in chondrosarcoma patients with higher histological grade and advanced MSTS stage. We also found that high expression of ZNF704 significantly correlated with a worse overall survival of chondrosarcoma patients. Multivariate Cox regression analysis indicated that ZNF704 was an independent prognostic marker in chondrosarcoma patients. Our in vitro studies demonstrated that knockdown of ZNF704 markedly inhibited chondrosarcoma cell viability, colony formation and induced apoptosis. In a nude mouse xenograft model, ZNF704 knockdown slowed down chondrosarcoma growth by inducing apoptosis in vivo. CONCLUSION: These findings suggest that ZNF704 may act as a potent oncogene implicated in chondrosarcoma development, and serve as a independent prognostic marker, highlight the potential of ZNF704 as a novel biomarker and therapeutic target for chondrosarcoma. |
format | Online Article Text |
id | pubmed-8232878 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-82328782021-06-28 Identification of ZNF704 as a Novel Oncogene and an Independent Prognostic Marker in Chondrosarcoma Chen, Changbao Zhou, Hua Zhang, Xiaolin Liu, Zhongjun Ma, Xinlong Cancer Manag Res Original Research PURPOSE: The transcription factor zinc finger protein 704 (ZNF704) is implicated in tumorigenesis. However, the underlying role of ZNF704 in the pathogenesis of chondrosarcoma remains not well delineated. This study investigates the expression level, prognostic significance and potential biological function of ZNF704 in human chondrosarcoma. MATERIALS AND METHODS: The mRNA and protein levels of ZNF704 in fresh chondrosarcomas and the paired adjacent non-tumor tissues were evaluated using real-time PCR and immunoblotting, respectively. The protein expression of ZNF704 in chondrosarcoma specimens was detected by immunohistochemistry, and the associations among its expression level, clinicopathological characteristics and prognosis were further investigated. Cell viability, colony formation and apoptosis assay were determined in chondrosarcoma cells and a xenograft model with ZNF704 knockdown. RESULTS: The expression levels of ZNF704 mRNA and protein in chondrosarcoma tissues were significantly higher than those in the paired adjacent non-tumor tissues and benign cartilage tumors. Clinicopathological analysis revealed that ZNF704 was expressed at higher levels in chondrosarcoma patients with higher histological grade and advanced MSTS stage. We also found that high expression of ZNF704 significantly correlated with a worse overall survival of chondrosarcoma patients. Multivariate Cox regression analysis indicated that ZNF704 was an independent prognostic marker in chondrosarcoma patients. Our in vitro studies demonstrated that knockdown of ZNF704 markedly inhibited chondrosarcoma cell viability, colony formation and induced apoptosis. In a nude mouse xenograft model, ZNF704 knockdown slowed down chondrosarcoma growth by inducing apoptosis in vivo. CONCLUSION: These findings suggest that ZNF704 may act as a potent oncogene implicated in chondrosarcoma development, and serve as a independent prognostic marker, highlight the potential of ZNF704 as a novel biomarker and therapeutic target for chondrosarcoma. Dove 2021-06-21 /pmc/articles/PMC8232878/ /pubmed/34188544 http://dx.doi.org/10.2147/CMAR.S313229 Text en © 2021 Chen et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Chen, Changbao Zhou, Hua Zhang, Xiaolin Liu, Zhongjun Ma, Xinlong Identification of ZNF704 as a Novel Oncogene and an Independent Prognostic Marker in Chondrosarcoma |
title | Identification of ZNF704 as a Novel Oncogene and an Independent Prognostic Marker in Chondrosarcoma |
title_full | Identification of ZNF704 as a Novel Oncogene and an Independent Prognostic Marker in Chondrosarcoma |
title_fullStr | Identification of ZNF704 as a Novel Oncogene and an Independent Prognostic Marker in Chondrosarcoma |
title_full_unstemmed | Identification of ZNF704 as a Novel Oncogene and an Independent Prognostic Marker in Chondrosarcoma |
title_short | Identification of ZNF704 as a Novel Oncogene and an Independent Prognostic Marker in Chondrosarcoma |
title_sort | identification of znf704 as a novel oncogene and an independent prognostic marker in chondrosarcoma |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8232878/ https://www.ncbi.nlm.nih.gov/pubmed/34188544 http://dx.doi.org/10.2147/CMAR.S313229 |
work_keys_str_mv | AT chenchangbao identificationofznf704asanoveloncogeneandanindependentprognosticmarkerinchondrosarcoma AT zhouhua identificationofznf704asanoveloncogeneandanindependentprognosticmarkerinchondrosarcoma AT zhangxiaolin identificationofznf704asanoveloncogeneandanindependentprognosticmarkerinchondrosarcoma AT liuzhongjun identificationofznf704asanoveloncogeneandanindependentprognosticmarkerinchondrosarcoma AT maxinlong identificationofznf704asanoveloncogeneandanindependentprognosticmarkerinchondrosarcoma |