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Knockdown of CDCA8 inhibits the proliferation and enhances the apoptosis of bladder cancer cells
Bladder cancer is a tumour of the urinary system with high mortality, and there is also a great lack of therapeutic targets in the clinic. Cell division cycle associated 8 (CDCA8), an important component of the vertebrate chromosomal passenger complex, is highly expressed in various tumours and prom...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PeerJ Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7194097/ https://www.ncbi.nlm.nih.gov/pubmed/32377458 http://dx.doi.org/10.7717/peerj.9078 |
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author | Gao, Xin Wen, Xiaohong He, Haowei Zheng, Linlin Yang, Yibo Yang, Jinlian Liu, Haifang Zhou, Xiguo Yang, Changshun Chen, Yinyi Chen, Mei Zhang, Shufang |
author_facet | Gao, Xin Wen, Xiaohong He, Haowei Zheng, Linlin Yang, Yibo Yang, Jinlian Liu, Haifang Zhou, Xiguo Yang, Changshun Chen, Yinyi Chen, Mei Zhang, Shufang |
author_sort | Gao, Xin |
collection | PubMed |
description | Bladder cancer is a tumour of the urinary system with high mortality, and there is also a great lack of therapeutic targets in the clinic. Cell division cycle associated 8 (CDCA8), an important component of the vertebrate chromosomal passenger complex, is highly expressed in various tumours and promotes tumour development. However, the role of CDCA8 in bladder cancer is not fully understood. This study aimed to reveal the function of CDCA8 in bladder cancer by determining the relationship between CDCA8 expression and proliferation, metastasis and apoptosis of bladder cancer cells. Firstly, we studied the mRNA expression of CDCA8 through the Gene Expression Omnibus (GEO) and the Cancer Genome Atlas (TCGA) databases and analysed the correlation between CDCA8 expression and prognosis of patients with bladder cancer. We also verified CDCA8 expression in bladder cancer tissues by immunohistochemistry. In addition, CDCA8 expression was inhibited in bladder cancer T24 and 5637 cells, and the effects of CDCA8 on the proliferation, migration and invasion of bladder cancer cell lines were investigated using cell counting kit-8, colony formation, cell cycle, apoptosis, wound healing and Transwell invasion assays. Results showed that CDCA8 was highly expressed in bladder cancer compared with normal tissues, and the high CDCA8 expression was significantly correlated with the poor prognosis of patients. Inhibiting CDCA8 expression inhibited the proliferation, migration and invasion of T24 and 5637 cells and induced the apoptosis of bladder cancer cells. CDCA8 was involved in the regulation of the growth cycle of bladder cancer cells. Bioinformatics-based mechanism analysis revealed that high CDCA8 expression may affect the cell cycle and P53 signalling pathways. In conclusion, our results suggest that CDCA8 is highly expressed in bladder cancer and can promote tumour development. Hence, CDCA8 may serve as an effective therapeutic target for treatment of bladder cancer. |
format | Online Article Text |
id | pubmed-7194097 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | PeerJ Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71940972020-05-06 Knockdown of CDCA8 inhibits the proliferation and enhances the apoptosis of bladder cancer cells Gao, Xin Wen, Xiaohong He, Haowei Zheng, Linlin Yang, Yibo Yang, Jinlian Liu, Haifang Zhou, Xiguo Yang, Changshun Chen, Yinyi Chen, Mei Zhang, Shufang PeerJ Molecular Biology Bladder cancer is a tumour of the urinary system with high mortality, and there is also a great lack of therapeutic targets in the clinic. Cell division cycle associated 8 (CDCA8), an important component of the vertebrate chromosomal passenger complex, is highly expressed in various tumours and promotes tumour development. However, the role of CDCA8 in bladder cancer is not fully understood. This study aimed to reveal the function of CDCA8 in bladder cancer by determining the relationship between CDCA8 expression and proliferation, metastasis and apoptosis of bladder cancer cells. Firstly, we studied the mRNA expression of CDCA8 through the Gene Expression Omnibus (GEO) and the Cancer Genome Atlas (TCGA) databases and analysed the correlation between CDCA8 expression and prognosis of patients with bladder cancer. We also verified CDCA8 expression in bladder cancer tissues by immunohistochemistry. In addition, CDCA8 expression was inhibited in bladder cancer T24 and 5637 cells, and the effects of CDCA8 on the proliferation, migration and invasion of bladder cancer cell lines were investigated using cell counting kit-8, colony formation, cell cycle, apoptosis, wound healing and Transwell invasion assays. Results showed that CDCA8 was highly expressed in bladder cancer compared with normal tissues, and the high CDCA8 expression was significantly correlated with the poor prognosis of patients. Inhibiting CDCA8 expression inhibited the proliferation, migration and invasion of T24 and 5637 cells and induced the apoptosis of bladder cancer cells. CDCA8 was involved in the regulation of the growth cycle of bladder cancer cells. Bioinformatics-based mechanism analysis revealed that high CDCA8 expression may affect the cell cycle and P53 signalling pathways. In conclusion, our results suggest that CDCA8 is highly expressed in bladder cancer and can promote tumour development. Hence, CDCA8 may serve as an effective therapeutic target for treatment of bladder cancer. PeerJ Inc. 2020-04-28 /pmc/articles/PMC7194097/ /pubmed/32377458 http://dx.doi.org/10.7717/peerj.9078 Text en © 2020 Gao et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited. |
spellingShingle | Molecular Biology Gao, Xin Wen, Xiaohong He, Haowei Zheng, Linlin Yang, Yibo Yang, Jinlian Liu, Haifang Zhou, Xiguo Yang, Changshun Chen, Yinyi Chen, Mei Zhang, Shufang Knockdown of CDCA8 inhibits the proliferation and enhances the apoptosis of bladder cancer cells |
title | Knockdown of CDCA8 inhibits the proliferation and enhances the apoptosis of bladder cancer cells |
title_full | Knockdown of CDCA8 inhibits the proliferation and enhances the apoptosis of bladder cancer cells |
title_fullStr | Knockdown of CDCA8 inhibits the proliferation and enhances the apoptosis of bladder cancer cells |
title_full_unstemmed | Knockdown of CDCA8 inhibits the proliferation and enhances the apoptosis of bladder cancer cells |
title_short | Knockdown of CDCA8 inhibits the proliferation and enhances the apoptosis of bladder cancer cells |
title_sort | knockdown of cdca8 inhibits the proliferation and enhances the apoptosis of bladder cancer cells |
topic | Molecular Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7194097/ https://www.ncbi.nlm.nih.gov/pubmed/32377458 http://dx.doi.org/10.7717/peerj.9078 |
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