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DZIP3 is a key factor to stratify IDH1 wild-type lower-grade gliomas
Background: Malignant glioma is the most common form of primary malignant brain cancer. Heterogeneity is the hallmark of glioma. DAZ-interacting zinc finger 3 (DZIP3), acts as an RNA-binding RING-type ubiquitin ligase; however, its function in glioma is yet unclear. Results: The DZIP3 expression was...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7803555/ https://www.ncbi.nlm.nih.gov/pubmed/33229627 http://dx.doi.org/10.18632/aging.103817 |
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author | Liang, Tingyu Zhou, Xingang Li, Peiliang You, Gan Wang, Fang Wang, Peng Feng, Enshan |
author_facet | Liang, Tingyu Zhou, Xingang Li, Peiliang You, Gan Wang, Fang Wang, Peng Feng, Enshan |
author_sort | Liang, Tingyu |
collection | PubMed |
description | Background: Malignant glioma is the most common form of primary malignant brain cancer. Heterogeneity is the hallmark of glioma. DAZ-interacting zinc finger 3 (DZIP3), acts as an RNA-binding RING-type ubiquitin ligase; however, its function in glioma is yet unclear. Results: The DZIP3 expression was related to the World Health Organization (WHO) grade and isocitrate dehydrogenase 1(IDH1) status, as well as the clinical outcome. Malignant cases exhibit lower DZIP3 expression. DZIP3 was an independent predictive factor of good prognosis in all grade and lower grade gliomas (p < 0.0001). Gene enrichment analysis and immunohistochemistry indicated that DZIP3 affected the biological behavior of glioma through the angiogenesis pathway. Moreover, based on DZIP3 expression, IDH1 wild-type lower-grade gliomas could be divided into two groups with different survival time. Conclusion: In conclusion, the loss of DZIP3 may be involved in the mechanism of angiogenesis in the invasive biological process of glioma. These findings laid an understanding of DZIP3-specific clinical features in glioma. Methods: A total of 325 glioma patients from the Chinese Glioma Genome Atlas (CGGA) RNA-seq cohort comprised the training cohort, while 265 patients from the GSE 16011 array cohort formed the validation cohort. The mRNA expression of DZIP3 and clinical characteristics was assessed. DZIP3 protein expression and microvessel density (MVD) were evaluated by immunohistochemistry (IHC). |
format | Online Article Text |
id | pubmed-7803555 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-78035552021-01-15 DZIP3 is a key factor to stratify IDH1 wild-type lower-grade gliomas Liang, Tingyu Zhou, Xingang Li, Peiliang You, Gan Wang, Fang Wang, Peng Feng, Enshan Aging (Albany NY) Research Paper Background: Malignant glioma is the most common form of primary malignant brain cancer. Heterogeneity is the hallmark of glioma. DAZ-interacting zinc finger 3 (DZIP3), acts as an RNA-binding RING-type ubiquitin ligase; however, its function in glioma is yet unclear. Results: The DZIP3 expression was related to the World Health Organization (WHO) grade and isocitrate dehydrogenase 1(IDH1) status, as well as the clinical outcome. Malignant cases exhibit lower DZIP3 expression. DZIP3 was an independent predictive factor of good prognosis in all grade and lower grade gliomas (p < 0.0001). Gene enrichment analysis and immunohistochemistry indicated that DZIP3 affected the biological behavior of glioma through the angiogenesis pathway. Moreover, based on DZIP3 expression, IDH1 wild-type lower-grade gliomas could be divided into two groups with different survival time. Conclusion: In conclusion, the loss of DZIP3 may be involved in the mechanism of angiogenesis in the invasive biological process of glioma. These findings laid an understanding of DZIP3-specific clinical features in glioma. Methods: A total of 325 glioma patients from the Chinese Glioma Genome Atlas (CGGA) RNA-seq cohort comprised the training cohort, while 265 patients from the GSE 16011 array cohort formed the validation cohort. The mRNA expression of DZIP3 and clinical characteristics was assessed. DZIP3 protein expression and microvessel density (MVD) were evaluated by immunohistochemistry (IHC). Impact Journals 2020-11-21 /pmc/articles/PMC7803555/ /pubmed/33229627 http://dx.doi.org/10.18632/aging.103817 Text en Copyright: © 2020 Liang et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Liang, Tingyu Zhou, Xingang Li, Peiliang You, Gan Wang, Fang Wang, Peng Feng, Enshan DZIP3 is a key factor to stratify IDH1 wild-type lower-grade gliomas |
title | DZIP3 is a key factor to stratify IDH1 wild-type lower-grade gliomas |
title_full | DZIP3 is a key factor to stratify IDH1 wild-type lower-grade gliomas |
title_fullStr | DZIP3 is a key factor to stratify IDH1 wild-type lower-grade gliomas |
title_full_unstemmed | DZIP3 is a key factor to stratify IDH1 wild-type lower-grade gliomas |
title_short | DZIP3 is a key factor to stratify IDH1 wild-type lower-grade gliomas |
title_sort | dzip3 is a key factor to stratify idh1 wild-type lower-grade gliomas |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7803555/ https://www.ncbi.nlm.nih.gov/pubmed/33229627 http://dx.doi.org/10.18632/aging.103817 |
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