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High brain acid soluble protein 1(BASP1) is a poor prognostic factor for cervical cancer and promotes tumor growth
BACKGROUND: The aim of this study was to determine whether brain abundant membrane attached signal protein 1 (BASP1) is a valuable prognostic biomarker for cervical cancer and whether BASP1 regulates the progression of cervical cancer. METHODS: Quantitative real-time PCR, western blotting, and immun...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5655910/ https://www.ncbi.nlm.nih.gov/pubmed/29089860 http://dx.doi.org/10.1186/s12935-017-0452-4 |
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author | Tang, Huiru Wang, Yan Zhang, Bing Xiong, Shiqiu Liu, Liangshuai Chen, Wei Tan, Guosheng Li, Heping |
author_facet | Tang, Huiru Wang, Yan Zhang, Bing Xiong, Shiqiu Liu, Liangshuai Chen, Wei Tan, Guosheng Li, Heping |
author_sort | Tang, Huiru |
collection | PubMed |
description | BACKGROUND: The aim of this study was to determine whether brain abundant membrane attached signal protein 1 (BASP1) is a valuable prognostic biomarker for cervical cancer and whether BASP1 regulates the progression of cervical cancer. METHODS: Quantitative real-time PCR, western blotting, and immunohistochemistry were used to determined BASP1 levels. Statistical analyses were used to examine whether BASP1 was a prognostic factor for patients with cervical cancer. The MTT assay, colony formation assay, cell cycle assay, anchorage-independent growth assay, and a tumor xenograft model were used to determine the role of BASP1 in the proliferation and tumorigenicity of cervical cancer. RESULTS: Brain abundant membrane attached signal protein 1 was upregulated in cervical cancer tissues and cells, and BASP1 expression levels were higher in patients that had died during follow-up compared with those that survived. There was a positive correlation between BASP1 expression and clinical stage (p < 0.001), T classification (p < 0.001), N classification (p < 0.05), and survival or mortality (p < 0.05). Patients with higher BASP1 expression had a shorter overall survival time. Cox regression analysis shown BSAP1 was an unfavorable prognostic factor for patients with cervical cancer. Overexpression of BASP1 promoted the proliferation of cervical cancer and its colony formation ability, accelerated cell cycle progression, and enhanced tumorgenicity. BASP1 knockdown inhibited the proliferation of cervical cancer and its colony formation ability, suppressed cell cycle progression, and decreased tumorgenicity. CONCLUSIONS: The results showed that BASP1 not only is a novel prognostic factor for patients with cervical cancer, but also promotes the proliferation and tumorigenicity of cervical cancer. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12935-017-0452-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5655910 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-56559102017-10-31 High brain acid soluble protein 1(BASP1) is a poor prognostic factor for cervical cancer and promotes tumor growth Tang, Huiru Wang, Yan Zhang, Bing Xiong, Shiqiu Liu, Liangshuai Chen, Wei Tan, Guosheng Li, Heping Cancer Cell Int Primary Research BACKGROUND: The aim of this study was to determine whether brain abundant membrane attached signal protein 1 (BASP1) is a valuable prognostic biomarker for cervical cancer and whether BASP1 regulates the progression of cervical cancer. METHODS: Quantitative real-time PCR, western blotting, and immunohistochemistry were used to determined BASP1 levels. Statistical analyses were used to examine whether BASP1 was a prognostic factor for patients with cervical cancer. The MTT assay, colony formation assay, cell cycle assay, anchorage-independent growth assay, and a tumor xenograft model were used to determine the role of BASP1 in the proliferation and tumorigenicity of cervical cancer. RESULTS: Brain abundant membrane attached signal protein 1 was upregulated in cervical cancer tissues and cells, and BASP1 expression levels were higher in patients that had died during follow-up compared with those that survived. There was a positive correlation between BASP1 expression and clinical stage (p < 0.001), T classification (p < 0.001), N classification (p < 0.05), and survival or mortality (p < 0.05). Patients with higher BASP1 expression had a shorter overall survival time. Cox regression analysis shown BSAP1 was an unfavorable prognostic factor for patients with cervical cancer. Overexpression of BASP1 promoted the proliferation of cervical cancer and its colony formation ability, accelerated cell cycle progression, and enhanced tumorgenicity. BASP1 knockdown inhibited the proliferation of cervical cancer and its colony formation ability, suppressed cell cycle progression, and decreased tumorgenicity. CONCLUSIONS: The results showed that BASP1 not only is a novel prognostic factor for patients with cervical cancer, but also promotes the proliferation and tumorigenicity of cervical cancer. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12935-017-0452-4) contains supplementary material, which is available to authorized users. BioMed Central 2017-10-24 /pmc/articles/PMC5655910/ /pubmed/29089860 http://dx.doi.org/10.1186/s12935-017-0452-4 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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. |
spellingShingle | Primary Research Tang, Huiru Wang, Yan Zhang, Bing Xiong, Shiqiu Liu, Liangshuai Chen, Wei Tan, Guosheng Li, Heping High brain acid soluble protein 1(BASP1) is a poor prognostic factor for cervical cancer and promotes tumor growth |
title | High brain acid soluble protein 1(BASP1) is a poor prognostic factor for cervical cancer and promotes tumor growth |
title_full | High brain acid soluble protein 1(BASP1) is a poor prognostic factor for cervical cancer and promotes tumor growth |
title_fullStr | High brain acid soluble protein 1(BASP1) is a poor prognostic factor for cervical cancer and promotes tumor growth |
title_full_unstemmed | High brain acid soluble protein 1(BASP1) is a poor prognostic factor for cervical cancer and promotes tumor growth |
title_short | High brain acid soluble protein 1(BASP1) is a poor prognostic factor for cervical cancer and promotes tumor growth |
title_sort | high brain acid soluble protein 1(basp1) is a poor prognostic factor for cervical cancer and promotes tumor growth |
topic | Primary Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5655910/ https://www.ncbi.nlm.nih.gov/pubmed/29089860 http://dx.doi.org/10.1186/s12935-017-0452-4 |
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