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In silico analysis and verification of S100 gene expression in gastric cancer

BACKGROUND: The S100 protein family comprises 22 members whose protein sequences encompass at least one EF-hand Ca(2+ )binding motif. They were involved in the regulation of a number of cellular processes such as cell cycle progression and differentiation. However, the expression status of S100 fami...

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Autores principales: Liu, Ji, Li, Xue, Dong, Guang-Long, Zhang, Hong-Wei, Chen, Dong-Li, Du, Jian-Jun, Zheng, Jian-Yong, Li, Ji-Peng, Wang, Wei-Zhong
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2567992/
https://www.ncbi.nlm.nih.gov/pubmed/18793447
http://dx.doi.org/10.1186/1471-2407-8-261
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author Liu, Ji
Li, Xue
Dong, Guang-Long
Zhang, Hong-Wei
Chen, Dong-Li
Du, Jian-Jun
Zheng, Jian-Yong
Li, Ji-Peng
Wang, Wei-Zhong
author_facet Liu, Ji
Li, Xue
Dong, Guang-Long
Zhang, Hong-Wei
Chen, Dong-Li
Du, Jian-Jun
Zheng, Jian-Yong
Li, Ji-Peng
Wang, Wei-Zhong
author_sort Liu, Ji
collection PubMed
description BACKGROUND: The S100 protein family comprises 22 members whose protein sequences encompass at least one EF-hand Ca(2+ )binding motif. They were involved in the regulation of a number of cellular processes such as cell cycle progression and differentiation. However, the expression status of S100 family members in gastric cancer was not known yet. METHODS: Combined with analysis of series analysis of gene expression, virtual Northern blot and microarray data, the expression levels of S100 family members in normal and malignant stomach tissues were systematically investigated. The expression of S100A3 was further evaluated by quantitative RT-PCR. RESULTS: At least 5 S100 genes were found to be upregulated in gastric cance by in silico analysis. Among them, four genes, including S100A2, S100A4, S100A7 and S100A10, were reported to overexpressed in gastric cancer previously. The expression of S100A3 in eighty patients of gastric cancer was further examined. The results showed that the mean expression levels of S100A3 in gastric cancer tissues were 2.5 times as high as in adjacent non-tumorous tissues. S100A3 expression was correlated with tumor differentiation and TNM (Tumor-Node-Metastasis) stage of gastric cancer, which was relatively highly expressed in poorly differentiated and advanced gastric cancer tissues (P < 0.05). CONCLUSION: To our knowledge this is the first report of systematic evaluation of S100 gene expressions in gastric cancers by multiple in silico analysis. The results indicated that overexpression of S100 gene family members were characteristics of gastric cancers and S100A3 might play important roles in differentiation and progression of gastric cancer.
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spelling pubmed-25679922008-10-16 In silico analysis and verification of S100 gene expression in gastric cancer Liu, Ji Li, Xue Dong, Guang-Long Zhang, Hong-Wei Chen, Dong-Li Du, Jian-Jun Zheng, Jian-Yong Li, Ji-Peng Wang, Wei-Zhong BMC Cancer Research Article BACKGROUND: The S100 protein family comprises 22 members whose protein sequences encompass at least one EF-hand Ca(2+ )binding motif. They were involved in the regulation of a number of cellular processes such as cell cycle progression and differentiation. However, the expression status of S100 family members in gastric cancer was not known yet. METHODS: Combined with analysis of series analysis of gene expression, virtual Northern blot and microarray data, the expression levels of S100 family members in normal and malignant stomach tissues were systematically investigated. The expression of S100A3 was further evaluated by quantitative RT-PCR. RESULTS: At least 5 S100 genes were found to be upregulated in gastric cance by in silico analysis. Among them, four genes, including S100A2, S100A4, S100A7 and S100A10, were reported to overexpressed in gastric cancer previously. The expression of S100A3 in eighty patients of gastric cancer was further examined. The results showed that the mean expression levels of S100A3 in gastric cancer tissues were 2.5 times as high as in adjacent non-tumorous tissues. S100A3 expression was correlated with tumor differentiation and TNM (Tumor-Node-Metastasis) stage of gastric cancer, which was relatively highly expressed in poorly differentiated and advanced gastric cancer tissues (P < 0.05). CONCLUSION: To our knowledge this is the first report of systematic evaluation of S100 gene expressions in gastric cancers by multiple in silico analysis. The results indicated that overexpression of S100 gene family members were characteristics of gastric cancers and S100A3 might play important roles in differentiation and progression of gastric cancer. BioMed Central 2008-09-16 /pmc/articles/PMC2567992/ /pubmed/18793447 http://dx.doi.org/10.1186/1471-2407-8-261 Text en Copyright © 2008 Liu et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Liu, Ji
Li, Xue
Dong, Guang-Long
Zhang, Hong-Wei
Chen, Dong-Li
Du, Jian-Jun
Zheng, Jian-Yong
Li, Ji-Peng
Wang, Wei-Zhong
In silico analysis and verification of S100 gene expression in gastric cancer
title In silico analysis and verification of S100 gene expression in gastric cancer
title_full In silico analysis and verification of S100 gene expression in gastric cancer
title_fullStr In silico analysis and verification of S100 gene expression in gastric cancer
title_full_unstemmed In silico analysis and verification of S100 gene expression in gastric cancer
title_short In silico analysis and verification of S100 gene expression in gastric cancer
title_sort in silico analysis and verification of s100 gene expression in gastric cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2567992/
https://www.ncbi.nlm.nih.gov/pubmed/18793447
http://dx.doi.org/10.1186/1471-2407-8-261
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