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Serum proteome profiling reveals SOX3 as a candidate prognostic marker for gastric cancer
Searching for the novel tumour biomarkers is pressing for gastric cancer diagnostication and prognostication. The serum specimens from patients diagnosed with locally advanced gastric carcinoma before operation and 4 week after surgery were collected, respectively, and serum proteome profiling was c...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7299728/ https://www.ncbi.nlm.nih.gov/pubmed/32363730 http://dx.doi.org/10.1111/jcmm.15326 |
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author | Shen, Jiajia Zhai, Jing Wu, Xinqian Xie, Guiping Shen, Lizong |
author_facet | Shen, Jiajia Zhai, Jing Wu, Xinqian Xie, Guiping Shen, Lizong |
author_sort | Shen, Jiajia |
collection | PubMed |
description | Searching for the novel tumour biomarkers is pressing for gastric cancer diagnostication and prognostication. The serum specimens from patients diagnosed with locally advanced gastric carcinoma before operation and 4 week after surgery were collected, respectively, and serum proteome profiling was conducted by liquid chromatography–mass spectrometry (MS)/MS. Fifty‐five proteins were identified to be up‐regulated and 16 proteins were down‐regulated, and these differentially expressed proteins participated in various biological processes. Serum levels of SOX3, one of down‐regulated proteins, in stomach cancer patients were higher than in healthy controls. SOX3 levels in cancer tissues were remarkably related to tumour differentiation, lymph node metastasis, primary tumour invasion and pTNM (pathological TNM) stage. Analysis with The Cancer Genome Atlas database indicated that SOX3 level and pTNM stage were the independent risk factors for the patient survival and that the overall survival was negatively associated with the SOX3 levels. Loss‐of‐function showed that SOX3 promoted gastric cancer cell invasion and migration in vitro and in vivo. SOX3 silence inhibits the expression of MMP9, and SOX3 is responsible for MMP9 expression transcriptionally. Our study highlights the potentiality of the paired pre‐ and post‐operation serum proteome signatures for the detection of biomarkers and reveals that SOX3 may serve as a candidate prognosis marker for gastric cancer. |
format | Online Article Text |
id | pubmed-7299728 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72997282020-06-18 Serum proteome profiling reveals SOX3 as a candidate prognostic marker for gastric cancer Shen, Jiajia Zhai, Jing Wu, Xinqian Xie, Guiping Shen, Lizong J Cell Mol Med Original Articles Searching for the novel tumour biomarkers is pressing for gastric cancer diagnostication and prognostication. The serum specimens from patients diagnosed with locally advanced gastric carcinoma before operation and 4 week after surgery were collected, respectively, and serum proteome profiling was conducted by liquid chromatography–mass spectrometry (MS)/MS. Fifty‐five proteins were identified to be up‐regulated and 16 proteins were down‐regulated, and these differentially expressed proteins participated in various biological processes. Serum levels of SOX3, one of down‐regulated proteins, in stomach cancer patients were higher than in healthy controls. SOX3 levels in cancer tissues were remarkably related to tumour differentiation, lymph node metastasis, primary tumour invasion and pTNM (pathological TNM) stage. Analysis with The Cancer Genome Atlas database indicated that SOX3 level and pTNM stage were the independent risk factors for the patient survival and that the overall survival was negatively associated with the SOX3 levels. Loss‐of‐function showed that SOX3 promoted gastric cancer cell invasion and migration in vitro and in vivo. SOX3 silence inhibits the expression of MMP9, and SOX3 is responsible for MMP9 expression transcriptionally. Our study highlights the potentiality of the paired pre‐ and post‐operation serum proteome signatures for the detection of biomarkers and reveals that SOX3 may serve as a candidate prognosis marker for gastric cancer. John Wiley and Sons Inc. 2020-05-04 2020-06 /pmc/articles/PMC7299728/ /pubmed/32363730 http://dx.doi.org/10.1111/jcmm.15326 Text en © 2020 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Shen, Jiajia Zhai, Jing Wu, Xinqian Xie, Guiping Shen, Lizong Serum proteome profiling reveals SOX3 as a candidate prognostic marker for gastric cancer |
title | Serum proteome profiling reveals SOX3 as a candidate prognostic marker for gastric cancer |
title_full | Serum proteome profiling reveals SOX3 as a candidate prognostic marker for gastric cancer |
title_fullStr | Serum proteome profiling reveals SOX3 as a candidate prognostic marker for gastric cancer |
title_full_unstemmed | Serum proteome profiling reveals SOX3 as a candidate prognostic marker for gastric cancer |
title_short | Serum proteome profiling reveals SOX3 as a candidate prognostic marker for gastric cancer |
title_sort | serum proteome profiling reveals sox3 as a candidate prognostic marker for gastric cancer |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7299728/ https://www.ncbi.nlm.nih.gov/pubmed/32363730 http://dx.doi.org/10.1111/jcmm.15326 |
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