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Increased expression of argininosuccinate synthetase protein predicts poor prognosis in human gastric cancer

Aberrant expression of argininosuccinate synthetase (ASS1, also known as ASS) has been found in cancer cells and is involved in the carcinogenesis of gastric cancer. The aim of the present study was to investigate the level of ASS expression in human gastric cancer and to determine the possible corr...

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Autores principales: SHAN, YAN-SHEN, HSU, HUI-PING, LAI, MING-DERG, YEN, MENG-CHI, LUO, YI-PEY, CHEN, YI-LING
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4254671/
https://www.ncbi.nlm.nih.gov/pubmed/25333458
http://dx.doi.org/10.3892/or.2014.3556
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author SHAN, YAN-SHEN
HSU, HUI-PING
LAI, MING-DERG
YEN, MENG-CHI
LUO, YI-PEY
CHEN, YI-LING
author_facet SHAN, YAN-SHEN
HSU, HUI-PING
LAI, MING-DERG
YEN, MENG-CHI
LUO, YI-PEY
CHEN, YI-LING
author_sort SHAN, YAN-SHEN
collection PubMed
description Aberrant expression of argininosuccinate synthetase (ASS1, also known as ASS) has been found in cancer cells and is involved in the carcinogenesis of gastric cancer. The aim of the present study was to investigate the level of ASS expression in human gastric cancer and to determine the possible correlations between ASS expression and clinicopathological findings. Immunohistochemistry was performed on paraffin-embedded tissues to determine whether ASS was expressed in 11 of 11 specimens from patients with gastric cancer. The protein was localized primarily to the cytoplasm of cancer cells and normal epithelium. In the Oncomine cancer microarray database, expression of the ASS gene was significantly increased in gastric cancer tissues. To investigate the clinicopathological and prognostic roles of ASS expression, we performed western blot analysis of 35 matched specimens of gastric adenocarcinomas and normal tissue obtained from patients treated at the National Cheng Kung University Hospital. The ratio of relative ASS expression (expressed as the ASS/β-actin ratio) in tumor tissues to that in normal tissues was correlated with large tumor size (P=0.007) and with the tumor, node, metastasis (TNM) stage of the American Joint Committee on Cancer staging system (P=0.031). Patients whose cancer had increased the relative expression of ASS were positive for perineural invasion and had poor recurrence-free survival. In summary, ASS expression in gastric cancer was associated with a poor prognosis. Further study of mechanisms to silence the ASS gene or decrease the enzymatic activity of ASS protein has the potential to provide new treatments for patients with gastric cancer.
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spelling pubmed-42546712014-12-05 Increased expression of argininosuccinate synthetase protein predicts poor prognosis in human gastric cancer SHAN, YAN-SHEN HSU, HUI-PING LAI, MING-DERG YEN, MENG-CHI LUO, YI-PEY CHEN, YI-LING Oncol Rep Articles Aberrant expression of argininosuccinate synthetase (ASS1, also known as ASS) has been found in cancer cells and is involved in the carcinogenesis of gastric cancer. The aim of the present study was to investigate the level of ASS expression in human gastric cancer and to determine the possible correlations between ASS expression and clinicopathological findings. Immunohistochemistry was performed on paraffin-embedded tissues to determine whether ASS was expressed in 11 of 11 specimens from patients with gastric cancer. The protein was localized primarily to the cytoplasm of cancer cells and normal epithelium. In the Oncomine cancer microarray database, expression of the ASS gene was significantly increased in gastric cancer tissues. To investigate the clinicopathological and prognostic roles of ASS expression, we performed western blot analysis of 35 matched specimens of gastric adenocarcinomas and normal tissue obtained from patients treated at the National Cheng Kung University Hospital. The ratio of relative ASS expression (expressed as the ASS/β-actin ratio) in tumor tissues to that in normal tissues was correlated with large tumor size (P=0.007) and with the tumor, node, metastasis (TNM) stage of the American Joint Committee on Cancer staging system (P=0.031). Patients whose cancer had increased the relative expression of ASS were positive for perineural invasion and had poor recurrence-free survival. In summary, ASS expression in gastric cancer was associated with a poor prognosis. Further study of mechanisms to silence the ASS gene or decrease the enzymatic activity of ASS protein has the potential to provide new treatments for patients with gastric cancer. D.A. Spandidos 2015-01 2014-10-20 /pmc/articles/PMC4254671/ /pubmed/25333458 http://dx.doi.org/10.3892/or.2014.3556 Text en Copyright © 2015, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
SHAN, YAN-SHEN
HSU, HUI-PING
LAI, MING-DERG
YEN, MENG-CHI
LUO, YI-PEY
CHEN, YI-LING
Increased expression of argininosuccinate synthetase protein predicts poor prognosis in human gastric cancer
title Increased expression of argininosuccinate synthetase protein predicts poor prognosis in human gastric cancer
title_full Increased expression of argininosuccinate synthetase protein predicts poor prognosis in human gastric cancer
title_fullStr Increased expression of argininosuccinate synthetase protein predicts poor prognosis in human gastric cancer
title_full_unstemmed Increased expression of argininosuccinate synthetase protein predicts poor prognosis in human gastric cancer
title_short Increased expression of argininosuccinate synthetase protein predicts poor prognosis in human gastric cancer
title_sort increased expression of argininosuccinate synthetase protein predicts poor prognosis in human gastric cancer
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4254671/
https://www.ncbi.nlm.nih.gov/pubmed/25333458
http://dx.doi.org/10.3892/or.2014.3556
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