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Overexpression of CCDC34 in colorectal cancer and its involvement in tumor growth, apoptosis and invasion

It has been previously reported that increased expression of coiled-coil domain containing 34 (CCDC34), a member of the CCDCs family, may promote the proliferation and invasion of bladder cancer cells. However, its role in colorectal cancer (CRC) remains unclear. The present study investigated CCDC3...

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Autores principales: Geng, Wei, Liang, Wei, Fan, Yanan, Ye, Zhibin, Zhang, Lixiao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5780142/
https://www.ncbi.nlm.nih.gov/pubmed/29115580
http://dx.doi.org/10.3892/mmr.2017.7860
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author Geng, Wei
Liang, Wei
Fan, Yanan
Ye, Zhibin
Zhang, Lixiao
author_facet Geng, Wei
Liang, Wei
Fan, Yanan
Ye, Zhibin
Zhang, Lixiao
author_sort Geng, Wei
collection PubMed
description It has been previously reported that increased expression of coiled-coil domain containing 34 (CCDC34), a member of the CCDCs family, may promote the proliferation and invasion of bladder cancer cells. However, its role in colorectal cancer (CRC) remains unclear. The present study investigated CCDC34 expression in CRC tissues and determined the association between CCDC34 expression and biological characteristics in patients with CRC. Additionally, the variation of cell activity, apoptosis, invasion and associated mechanisms were evaluated following CCDC34 inhibition in SW620 cells with small interfering RNA (siRNA). The role of CCDC34 in CRC growth, apoptosis and invasion was investigated. In the current study, immunohistochemistry revealed an overexpression of CCDC34 in CRC tissues compared with paracancerous tissue (χ(2)=29.810; P<0.001). Furthermore, CCDC34 expression was revealed to be associated with tumor invasion depth and lymphatic metastasis (χ(2)=4.343, P=0.037; χ(2)=7.915, P=0.005). Additionally, the inhibition of CCDC34 expression in SW620 cells led to reduced tumor cell activity, increased apoptosis rate and reduced invasion ability, and expression of apoptosis and invasion-associated genes varied simultaneously which demonstrated that B cell leukemia/lymphoma 2, survivin, N-cadherin, and MMP-9 were decreased, whereas E-cadherin increased significantly in cells of CCDC34-siRNA group compared with the control group (P<0.05). Therefore, CCDC34 may contribute to CRC development by inhibiting apoptosis of cancer cells and promoting invasion.
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spelling pubmed-57801422018-02-05 Overexpression of CCDC34 in colorectal cancer and its involvement in tumor growth, apoptosis and invasion Geng, Wei Liang, Wei Fan, Yanan Ye, Zhibin Zhang, Lixiao Mol Med Rep Articles It has been previously reported that increased expression of coiled-coil domain containing 34 (CCDC34), a member of the CCDCs family, may promote the proliferation and invasion of bladder cancer cells. However, its role in colorectal cancer (CRC) remains unclear. The present study investigated CCDC34 expression in CRC tissues and determined the association between CCDC34 expression and biological characteristics in patients with CRC. Additionally, the variation of cell activity, apoptosis, invasion and associated mechanisms were evaluated following CCDC34 inhibition in SW620 cells with small interfering RNA (siRNA). The role of CCDC34 in CRC growth, apoptosis and invasion was investigated. In the current study, immunohistochemistry revealed an overexpression of CCDC34 in CRC tissues compared with paracancerous tissue (χ(2)=29.810; P<0.001). Furthermore, CCDC34 expression was revealed to be associated with tumor invasion depth and lymphatic metastasis (χ(2)=4.343, P=0.037; χ(2)=7.915, P=0.005). Additionally, the inhibition of CCDC34 expression in SW620 cells led to reduced tumor cell activity, increased apoptosis rate and reduced invasion ability, and expression of apoptosis and invasion-associated genes varied simultaneously which demonstrated that B cell leukemia/lymphoma 2, survivin, N-cadherin, and MMP-9 were decreased, whereas E-cadherin increased significantly in cells of CCDC34-siRNA group compared with the control group (P<0.05). Therefore, CCDC34 may contribute to CRC development by inhibiting apoptosis of cancer cells and promoting invasion. D.A. Spandidos 2018-01 2017-10-24 /pmc/articles/PMC5780142/ /pubmed/29115580 http://dx.doi.org/10.3892/mmr.2017.7860 Text en Copyright: © Geng et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Geng, Wei
Liang, Wei
Fan, Yanan
Ye, Zhibin
Zhang, Lixiao
Overexpression of CCDC34 in colorectal cancer and its involvement in tumor growth, apoptosis and invasion
title Overexpression of CCDC34 in colorectal cancer and its involvement in tumor growth, apoptosis and invasion
title_full Overexpression of CCDC34 in colorectal cancer and its involvement in tumor growth, apoptosis and invasion
title_fullStr Overexpression of CCDC34 in colorectal cancer and its involvement in tumor growth, apoptosis and invasion
title_full_unstemmed Overexpression of CCDC34 in colorectal cancer and its involvement in tumor growth, apoptosis and invasion
title_short Overexpression of CCDC34 in colorectal cancer and its involvement in tumor growth, apoptosis and invasion
title_sort overexpression of ccdc34 in colorectal cancer and its involvement in tumor growth, apoptosis and invasion
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5780142/
https://www.ncbi.nlm.nih.gov/pubmed/29115580
http://dx.doi.org/10.3892/mmr.2017.7860
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