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Expression of centrosomal protein 55 in glioma tissue and the influence on glioma cell functions

BACKGROUND: Centrosomal protein 55 (CEP55) protein has high expression levels in various tumors and plays important regulatory effects on cell cycle. We aimed to detect the expressions of CEP55 in glioma tissues, and to evaluate the effects on glioma cell functions and apoptosis. METHODS: Fifty fres...

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Autores principales: Xu, Yifan, Lu, Tianyu, Xu, Wu, Chen, Weitao, Liang, Weibang, Jin, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8799232/
https://www.ncbi.nlm.nih.gov/pubmed/35116751
http://dx.doi.org/10.21037/tcr.2019.01.33
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author Xu, Yifan
Lu, Tianyu
Xu, Wu
Chen, Weitao
Liang, Weibang
Jin, Wei
author_facet Xu, Yifan
Lu, Tianyu
Xu, Wu
Chen, Weitao
Liang, Weibang
Jin, Wei
author_sort Xu, Yifan
collection PubMed
description BACKGROUND: Centrosomal protein 55 (CEP55) protein has high expression levels in various tumors and plays important regulatory effects on cell cycle. We aimed to detect the expressions of CEP55 in glioma tissues, and to evaluate the effects on glioma cell functions and apoptosis. METHODS: Fifty fresh astrocytoma tissue samples resected from surgeries were collected, and twenty normal brain tissue samples were obtained as a control group. CEP55 protein expressions were measured by Western blot and immunohistochemical assay. After siRNA interference, the proliferation, migration, invasion and apoptosis of glioma cell lines LN229/T98G were detected by MTT assay, scratch assay, Transwell assay and flow cytometry respectively. RESULTS: The expression level of CEP55 protein in glioma tissue was significantly higher than that in normal control group, and the expressions in glioma tissues were elevated with increasing grade. Glioma cell lines in which CEP55 expression was stably knocked down were successfully constructed. MTT assay showed that the growth of these cells was significantly slowed down compared with that of normal cells. Scratch assay exhibited that their migration capability significantly decreased. Transwell assay revealed that the invasive ability was also attenuated with decreasing CEP55 expression. Flow cytometry showed that down-regulated expression of CEP55 promoted the apoptosis of LN229/T98G cells. CONCLUSIONS: CEP55 expression increased in glioma tissues. After interference of its expression, glioma cell functions were significantly weakened, and apoptosis was facilitated. CEP55 may be a molecular marker for glioma diagnosis or a new target for molecular therapy.
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spelling pubmed-87992322022-02-02 Expression of centrosomal protein 55 in glioma tissue and the influence on glioma cell functions Xu, Yifan Lu, Tianyu Xu, Wu Chen, Weitao Liang, Weibang Jin, Wei Transl Cancer Res Original Article BACKGROUND: Centrosomal protein 55 (CEP55) protein has high expression levels in various tumors and plays important regulatory effects on cell cycle. We aimed to detect the expressions of CEP55 in glioma tissues, and to evaluate the effects on glioma cell functions and apoptosis. METHODS: Fifty fresh astrocytoma tissue samples resected from surgeries were collected, and twenty normal brain tissue samples were obtained as a control group. CEP55 protein expressions were measured by Western blot and immunohistochemical assay. After siRNA interference, the proliferation, migration, invasion and apoptosis of glioma cell lines LN229/T98G were detected by MTT assay, scratch assay, Transwell assay and flow cytometry respectively. RESULTS: The expression level of CEP55 protein in glioma tissue was significantly higher than that in normal control group, and the expressions in glioma tissues were elevated with increasing grade. Glioma cell lines in which CEP55 expression was stably knocked down were successfully constructed. MTT assay showed that the growth of these cells was significantly slowed down compared with that of normal cells. Scratch assay exhibited that their migration capability significantly decreased. Transwell assay revealed that the invasive ability was also attenuated with decreasing CEP55 expression. Flow cytometry showed that down-regulated expression of CEP55 promoted the apoptosis of LN229/T98G cells. CONCLUSIONS: CEP55 expression increased in glioma tissues. After interference of its expression, glioma cell functions were significantly weakened, and apoptosis was facilitated. CEP55 may be a molecular marker for glioma diagnosis or a new target for molecular therapy. AME Publishing Company 2019-02 /pmc/articles/PMC8799232/ /pubmed/35116751 http://dx.doi.org/10.21037/tcr.2019.01.33 Text en 2019 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
spellingShingle Original Article
Xu, Yifan
Lu, Tianyu
Xu, Wu
Chen, Weitao
Liang, Weibang
Jin, Wei
Expression of centrosomal protein 55 in glioma tissue and the influence on glioma cell functions
title Expression of centrosomal protein 55 in glioma tissue and the influence on glioma cell functions
title_full Expression of centrosomal protein 55 in glioma tissue and the influence on glioma cell functions
title_fullStr Expression of centrosomal protein 55 in glioma tissue and the influence on glioma cell functions
title_full_unstemmed Expression of centrosomal protein 55 in glioma tissue and the influence on glioma cell functions
title_short Expression of centrosomal protein 55 in glioma tissue and the influence on glioma cell functions
title_sort expression of centrosomal protein 55 in glioma tissue and the influence on glioma cell functions
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8799232/
https://www.ncbi.nlm.nih.gov/pubmed/35116751
http://dx.doi.org/10.21037/tcr.2019.01.33
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