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AKR1B10 expression predicts response of gastric cancer to neoadjuvant chemotherapy
Effective methods for predicting tumor response to preoperative chemotherapy are required. Aldo-ketoreductase family 1 member B10 (AKR1B10) is predominantly expressed in the gastrointestinal tract and serves an important function in cancer development and progression. The present study investigated...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6313001/ https://www.ncbi.nlm.nih.gov/pubmed/30655829 http://dx.doi.org/10.3892/ol.2018.9705 |
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author | Ahmed, Syed Minhaj Uddin Jiang, Zi Nong Zheng, Zhao Hong Li, Yulong Wang, Xiu Jun Tang, Xiuwen |
author_facet | Ahmed, Syed Minhaj Uddin Jiang, Zi Nong Zheng, Zhao Hong Li, Yulong Wang, Xiu Jun Tang, Xiuwen |
author_sort | Ahmed, Syed Minhaj Uddin |
collection | PubMed |
description | Effective methods for predicting tumor response to preoperative chemotherapy are required. Aldo-ketoreductase family 1 member B10 (AKR1B10) is predominantly expressed in the gastrointestinal tract and serves an important function in cancer development and progression. The present study investigated whether AKR1B10 expression may predict the therapeutic response of locally advanced gastric cancer. A total of 53 patients with gastric cancer underwent neoadjuvant chemotherapy followed by surgery between January 2006 and December 2015. The protein expression level of AKR1B10 was determined in paraffin-embedded biopsy specimens using immunohistochemistry. Western blotting confirmed that the AKR1B10 protein is primarily localized to the cytoplasm. χ(2) and Fisher's exact tests were used to determine the association of AKR1B10 with a number of clinic opathological features. Univariate and multivariate analyses were used to identify the prognostic factors. Survival rates were compared using Kaplan-Meier curves with a log-rank test. The positive rate of AKR1B10 protein expression was 58.5%, whereas 41.5% samples exhibited negative expression. The frequency of AKR1B10-positive gastric cancer samples was increased in patients with lymph node metastasis and decreased in those exhibiting tumor regression. The 5-years overall survival rate for the AKR1B10-positive group was significantly poorer than that for the AKR1B10-negative group. AKR1B10 expression was associated with lymph node metastasis and a poorer prognosis, along with a poor response to neoadjuvant chemotherapy suggesting that AKR1B10 may be a potential predictor for the therapeutic response of locally-advanced gastric cancer. |
format | Online Article Text |
id | pubmed-6313001 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-63130012019-01-17 AKR1B10 expression predicts response of gastric cancer to neoadjuvant chemotherapy Ahmed, Syed Minhaj Uddin Jiang, Zi Nong Zheng, Zhao Hong Li, Yulong Wang, Xiu Jun Tang, Xiuwen Oncol Lett Articles Effective methods for predicting tumor response to preoperative chemotherapy are required. Aldo-ketoreductase family 1 member B10 (AKR1B10) is predominantly expressed in the gastrointestinal tract and serves an important function in cancer development and progression. The present study investigated whether AKR1B10 expression may predict the therapeutic response of locally advanced gastric cancer. A total of 53 patients with gastric cancer underwent neoadjuvant chemotherapy followed by surgery between January 2006 and December 2015. The protein expression level of AKR1B10 was determined in paraffin-embedded biopsy specimens using immunohistochemistry. Western blotting confirmed that the AKR1B10 protein is primarily localized to the cytoplasm. χ(2) and Fisher's exact tests were used to determine the association of AKR1B10 with a number of clinic opathological features. Univariate and multivariate analyses were used to identify the prognostic factors. Survival rates were compared using Kaplan-Meier curves with a log-rank test. The positive rate of AKR1B10 protein expression was 58.5%, whereas 41.5% samples exhibited negative expression. The frequency of AKR1B10-positive gastric cancer samples was increased in patients with lymph node metastasis and decreased in those exhibiting tumor regression. The 5-years overall survival rate for the AKR1B10-positive group was significantly poorer than that for the AKR1B10-negative group. AKR1B10 expression was associated with lymph node metastasis and a poorer prognosis, along with a poor response to neoadjuvant chemotherapy suggesting that AKR1B10 may be a potential predictor for the therapeutic response of locally-advanced gastric cancer. D.A. Spandidos 2019-01 2018-11-15 /pmc/articles/PMC6313001/ /pubmed/30655829 http://dx.doi.org/10.3892/ol.2018.9705 Text en Copyright: © Ahmed et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Ahmed, Syed Minhaj Uddin Jiang, Zi Nong Zheng, Zhao Hong Li, Yulong Wang, Xiu Jun Tang, Xiuwen AKR1B10 expression predicts response of gastric cancer to neoadjuvant chemotherapy |
title | AKR1B10 expression predicts response of gastric cancer to neoadjuvant chemotherapy |
title_full | AKR1B10 expression predicts response of gastric cancer to neoadjuvant chemotherapy |
title_fullStr | AKR1B10 expression predicts response of gastric cancer to neoadjuvant chemotherapy |
title_full_unstemmed | AKR1B10 expression predicts response of gastric cancer to neoadjuvant chemotherapy |
title_short | AKR1B10 expression predicts response of gastric cancer to neoadjuvant chemotherapy |
title_sort | akr1b10 expression predicts response of gastric cancer to neoadjuvant chemotherapy |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6313001/ https://www.ncbi.nlm.nih.gov/pubmed/30655829 http://dx.doi.org/10.3892/ol.2018.9705 |
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