Cargando…

Identification of specific biomarkers for gastric adenocarcinoma by ITRAQ proteomic approach

The aim of this study was to identify biomarkers for gastric cancer (GC) by iTRAQ. Using proteins extracted from a panel of 4 pairs of gastric adenocarcinoma samples (stage III-IV, Her-2 negative), we identified 10 up regulated and 9 down regulated proteins in all four pairs of GC samples compared t...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Xiaoxiao, Zhi, Qiaoming, Liu, Songbai, Xue, Sheng-Li, Shen, Congcong, Li, Yangxin, Wu, Chaofan, Tang, Zaixiang, Chen, Weichang, Song, Jenny Lee, Bao, Meiyu, Song, Yao-Hua, Zhou, Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5150883/
https://www.ncbi.nlm.nih.gov/pubmed/27941907
http://dx.doi.org/10.1038/srep38871
_version_ 1782474281248096256
author Wang, Xiaoxiao
Zhi, Qiaoming
Liu, Songbai
Xue, Sheng-Li
Shen, Congcong
Li, Yangxin
Wu, Chaofan
Tang, Zaixiang
Chen, Weichang
Song, Jenny Lee
Bao, Meiyu
Song, Yao-Hua
Zhou, Jin
author_facet Wang, Xiaoxiao
Zhi, Qiaoming
Liu, Songbai
Xue, Sheng-Li
Shen, Congcong
Li, Yangxin
Wu, Chaofan
Tang, Zaixiang
Chen, Weichang
Song, Jenny Lee
Bao, Meiyu
Song, Yao-Hua
Zhou, Jin
author_sort Wang, Xiaoxiao
collection PubMed
description The aim of this study was to identify biomarkers for gastric cancer (GC) by iTRAQ. Using proteins extracted from a panel of 4 pairs of gastric adenocarcinoma samples (stage III-IV, Her-2 negative), we identified 10 up regulated and 9 down regulated proteins in all four pairs of GC samples compared to adjacent normal gastric tissue. The up regulated proteins are mainly involved in cell motility, while the down regulated proteins are mitochondrial enzymes involved in energy metabolism. The expression of three up regulated proteins (ANXA1, NNMT, fibulin-5) and one of the down regulated proteins (UQCRC1) was validated by Western Blot in 97 GC samples. ANXA1 was up regulated in 61.36% of stage I/II GC samples compared to matched adjacent normal gastric tissue, and its expression increased further in stage III/IV samples. Knockdown of ANXA1 by siRNA significantly inhibited GC cell migration and invasion, whereas over expression of ANXA1 promoted migration and invasion. We found decreased expression of UQCRC1 in all stages of GC samples. Our data suggest that increased cell motility and decreased mitochondrial energy metabolism are important hallmarks during the development of GC.
format Online
Article
Text
id pubmed-5150883
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-51508832016-12-19 Identification of specific biomarkers for gastric adenocarcinoma by ITRAQ proteomic approach Wang, Xiaoxiao Zhi, Qiaoming Liu, Songbai Xue, Sheng-Li Shen, Congcong Li, Yangxin Wu, Chaofan Tang, Zaixiang Chen, Weichang Song, Jenny Lee Bao, Meiyu Song, Yao-Hua Zhou, Jin Sci Rep Article The aim of this study was to identify biomarkers for gastric cancer (GC) by iTRAQ. Using proteins extracted from a panel of 4 pairs of gastric adenocarcinoma samples (stage III-IV, Her-2 negative), we identified 10 up regulated and 9 down regulated proteins in all four pairs of GC samples compared to adjacent normal gastric tissue. The up regulated proteins are mainly involved in cell motility, while the down regulated proteins are mitochondrial enzymes involved in energy metabolism. The expression of three up regulated proteins (ANXA1, NNMT, fibulin-5) and one of the down regulated proteins (UQCRC1) was validated by Western Blot in 97 GC samples. ANXA1 was up regulated in 61.36% of stage I/II GC samples compared to matched adjacent normal gastric tissue, and its expression increased further in stage III/IV samples. Knockdown of ANXA1 by siRNA significantly inhibited GC cell migration and invasion, whereas over expression of ANXA1 promoted migration and invasion. We found decreased expression of UQCRC1 in all stages of GC samples. Our data suggest that increased cell motility and decreased mitochondrial energy metabolism are important hallmarks during the development of GC. Nature Publishing Group 2016-12-12 /pmc/articles/PMC5150883/ /pubmed/27941907 http://dx.doi.org/10.1038/srep38871 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Wang, Xiaoxiao
Zhi, Qiaoming
Liu, Songbai
Xue, Sheng-Li
Shen, Congcong
Li, Yangxin
Wu, Chaofan
Tang, Zaixiang
Chen, Weichang
Song, Jenny Lee
Bao, Meiyu
Song, Yao-Hua
Zhou, Jin
Identification of specific biomarkers for gastric adenocarcinoma by ITRAQ proteomic approach
title Identification of specific biomarkers for gastric adenocarcinoma by ITRAQ proteomic approach
title_full Identification of specific biomarkers for gastric adenocarcinoma by ITRAQ proteomic approach
title_fullStr Identification of specific biomarkers for gastric adenocarcinoma by ITRAQ proteomic approach
title_full_unstemmed Identification of specific biomarkers for gastric adenocarcinoma by ITRAQ proteomic approach
title_short Identification of specific biomarkers for gastric adenocarcinoma by ITRAQ proteomic approach
title_sort identification of specific biomarkers for gastric adenocarcinoma by itraq proteomic approach
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5150883/
https://www.ncbi.nlm.nih.gov/pubmed/27941907
http://dx.doi.org/10.1038/srep38871
work_keys_str_mv AT wangxiaoxiao identificationofspecificbiomarkersforgastricadenocarcinomabyitraqproteomicapproach
AT zhiqiaoming identificationofspecificbiomarkersforgastricadenocarcinomabyitraqproteomicapproach
AT liusongbai identificationofspecificbiomarkersforgastricadenocarcinomabyitraqproteomicapproach
AT xueshengli identificationofspecificbiomarkersforgastricadenocarcinomabyitraqproteomicapproach
AT shencongcong identificationofspecificbiomarkersforgastricadenocarcinomabyitraqproteomicapproach
AT liyangxin identificationofspecificbiomarkersforgastricadenocarcinomabyitraqproteomicapproach
AT wuchaofan identificationofspecificbiomarkersforgastricadenocarcinomabyitraqproteomicapproach
AT tangzaixiang identificationofspecificbiomarkersforgastricadenocarcinomabyitraqproteomicapproach
AT chenweichang identificationofspecificbiomarkersforgastricadenocarcinomabyitraqproteomicapproach
AT songjennylee identificationofspecificbiomarkersforgastricadenocarcinomabyitraqproteomicapproach
AT baomeiyu identificationofspecificbiomarkersforgastricadenocarcinomabyitraqproteomicapproach
AT songyaohua identificationofspecificbiomarkersforgastricadenocarcinomabyitraqproteomicapproach
AT zhoujin identificationofspecificbiomarkersforgastricadenocarcinomabyitraqproteomicapproach