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Overexpression of SAPCD2 correlates with proliferation and invasion of colorectal carcinoma cells

BACKGROUND: Suppressor anaphase-promoting complex domain containing 2 (SAPCD2) is a novel gene playing important roles in the initiation, invasion, and metastasis of several malignancies. However, its role in colorectal carcinoma (CRC) still remains unclear. METHOD: In this study, we investigated th...

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Autores principales: Luo, Yage, Wang, Lili, Ran, Wenwen, Li, Guangqi, Xiao, Yujing, Wang, Xiaonan, Zhao, Han, Xing, Xiaoming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7006392/
https://www.ncbi.nlm.nih.gov/pubmed/32055236
http://dx.doi.org/10.1186/s12935-020-1121-6
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author Luo, Yage
Wang, Lili
Ran, Wenwen
Li, Guangqi
Xiao, Yujing
Wang, Xiaonan
Zhao, Han
Xing, Xiaoming
author_facet Luo, Yage
Wang, Lili
Ran, Wenwen
Li, Guangqi
Xiao, Yujing
Wang, Xiaonan
Zhao, Han
Xing, Xiaoming
author_sort Luo, Yage
collection PubMed
description BACKGROUND: Suppressor anaphase-promoting complex domain containing 2 (SAPCD2) is a novel gene playing important roles in the initiation, invasion, and metastasis of several malignancies. However, its role in colorectal carcinoma (CRC) still remains unclear. METHOD: In this study, we investigated the expression and biological function of SAPCD2 in CRC. Immunohistochemistry (IHC) for SAPCD2 was performed in 410 pairs of CRC specimens and corresponding normal epithelial tissues, and in 50 adenoma tissues. Clinical pathological factors were analyzed in relation to the expression of SAPCD2. The biological functions of SAPCD2 in CRC cells and its effect on cell cycle were investigated in vitro and in vivo through gain/loss-of-function approaches. RESULTS: IHC showed that SAPCD2 expression was significantly higher in CRC tissues compared to adenoma and normal epithelium tissues and was correlated with tumor location (p = 0.018). SAPCD2 significantly promoted cell proliferation, migration, and invasion both in vitro and in vivo (p < 0.05). In addition, SAPCD2 knockdown in CRC cells was associated with reduced G(1)/S transition, while overexpression caused G(2)/M phase arrest (p < 0.05). CONCLUSIONS: In sum, SAPCD2 is overexpressed in CRC tissues and plays a critical role in CRC progression. Therefore, it might represent a promising therapeutic target for CRC treatment.
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spelling pubmed-70063922020-02-13 Overexpression of SAPCD2 correlates with proliferation and invasion of colorectal carcinoma cells Luo, Yage Wang, Lili Ran, Wenwen Li, Guangqi Xiao, Yujing Wang, Xiaonan Zhao, Han Xing, Xiaoming Cancer Cell Int Primary Research BACKGROUND: Suppressor anaphase-promoting complex domain containing 2 (SAPCD2) is a novel gene playing important roles in the initiation, invasion, and metastasis of several malignancies. However, its role in colorectal carcinoma (CRC) still remains unclear. METHOD: In this study, we investigated the expression and biological function of SAPCD2 in CRC. Immunohistochemistry (IHC) for SAPCD2 was performed in 410 pairs of CRC specimens and corresponding normal epithelial tissues, and in 50 adenoma tissues. Clinical pathological factors were analyzed in relation to the expression of SAPCD2. The biological functions of SAPCD2 in CRC cells and its effect on cell cycle were investigated in vitro and in vivo through gain/loss-of-function approaches. RESULTS: IHC showed that SAPCD2 expression was significantly higher in CRC tissues compared to adenoma and normal epithelium tissues and was correlated with tumor location (p = 0.018). SAPCD2 significantly promoted cell proliferation, migration, and invasion both in vitro and in vivo (p < 0.05). In addition, SAPCD2 knockdown in CRC cells was associated with reduced G(1)/S transition, while overexpression caused G(2)/M phase arrest (p < 0.05). CONCLUSIONS: In sum, SAPCD2 is overexpressed in CRC tissues and plays a critical role in CRC progression. Therefore, it might represent a promising therapeutic target for CRC treatment. BioMed Central 2020-02-06 /pmc/articles/PMC7006392/ /pubmed/32055236 http://dx.doi.org/10.1186/s12935-020-1121-6 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Primary Research
Luo, Yage
Wang, Lili
Ran, Wenwen
Li, Guangqi
Xiao, Yujing
Wang, Xiaonan
Zhao, Han
Xing, Xiaoming
Overexpression of SAPCD2 correlates with proliferation and invasion of colorectal carcinoma cells
title Overexpression of SAPCD2 correlates with proliferation and invasion of colorectal carcinoma cells
title_full Overexpression of SAPCD2 correlates with proliferation and invasion of colorectal carcinoma cells
title_fullStr Overexpression of SAPCD2 correlates with proliferation and invasion of colorectal carcinoma cells
title_full_unstemmed Overexpression of SAPCD2 correlates with proliferation and invasion of colorectal carcinoma cells
title_short Overexpression of SAPCD2 correlates with proliferation and invasion of colorectal carcinoma cells
title_sort overexpression of sapcd2 correlates with proliferation and invasion of colorectal carcinoma cells
topic Primary Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7006392/
https://www.ncbi.nlm.nih.gov/pubmed/32055236
http://dx.doi.org/10.1186/s12935-020-1121-6
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