High expression of SLC34A2 is a favorable prognostic marker in lung adenocarcinoma patients

Dysregulation of SLC34A2 (NaPi2b) in tumors has attracted wide attention, but its expression and function in non–small cell lung cancer remains unclear. By examining its expression in lung adenocarcinoma and correlation to patient outcome, we aimed to explore its prognostic and therapeutic values in...

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Main Authors: Zhaoxuan Zhang, Shan Ye, Min Zhang, Jing Wu, Hong Yan, Xiaojie Li, Jie He
Format: Article
Language:English
Published: IOS Press 2017-07-01
Series:Tumor Biology
Online Access:https://doi.org/10.1177/1010428317720212
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spelling doaj-3a0843e9f5614107aad07308069aa0ee2021-05-03T00:43:31ZengIOS PressTumor Biology1423-03802017-07-013910.1177/1010428317720212High expression of SLC34A2 is a favorable prognostic marker in lung adenocarcinoma patientsZhaoxuan Zhang0Shan Ye1Min Zhang2Jing Wu3Hong Yan4Xiaojie Li5Jie He6Department of Pathology, Anhui Provincial Cancer Hospital, Hefei, P.R. ChinaDepartment of Pathology, Anhui Provincial Cancer Hospital, Hefei, P.R. ChinaDepartment of Pathology, Anhui Provincial Cancer Hospital, Hefei, P.R. ChinaDepartment of Pathology, Anhui Provincial Cancer Hospital, Hefei, P.R. ChinaDepartment of Pathology, Anhui Provincial Cancer Hospital, Hefei, P.R. ChinaDepartment of Pathology, Anhui Provincial Cancer Hospital, Hefei, P.R. ChinaDepartment of Pathology, Anhui Provincial Cancer Hospital, Hefei, P.R. ChinaDysregulation of SLC34A2 (NaPi2b) in tumors has attracted wide attention, but its expression and function in non–small cell lung cancer remains unclear. By examining its expression in lung adenocarcinoma and correlation to patient outcome, we aimed to explore its prognostic and therapeutic values in this deadly disease. Overall, 175 cases of lung adenocarcinoma sample were included in this study. Histological subtyping of them was diagnosed according to standards of the International Association for the Study of Lung Cancer/American Thoracic Society/European Respiratory Society in 2011. Protein expression of SLC34A2 and anaplastic lymphoma kinase in these samples was determined by immunohistochemistry. Epidermal growth factor receptor mutations were examined using amplification refractory mutation system. Statistical analysis was performed using software of Pearson’s correlation coefficient. High expression of SLC34A2 was identified in about 2/3 patients and correlated with significantly better patient’s overall survival. Epidermal growth factor receptor mutations were detected in about 53% of patients with no statistically significant difference to patient’s overall survival. Anaplastic lymphoma kinase rearrangement was found in 8 out of 175 patients, harboring this abnormality leads to shorter overall survival. No correlation has been found between SLC34A2 expression and epidermal growth factor receptor mutation or anaplastic lymphoma kinase rearrangements in lung adenocarcinoma. High expression of SLC34A2 is present in about 3/4 lung adenocarcinoma samples and predicts better outcome. Since it is a membrane protein, antibody-based drugs targeting this marker might bring new resolution to this deadly disease.https://doi.org/10.1177/1010428317720212
collection DOAJ
language English
format Article
sources DOAJ
author Zhaoxuan Zhang
Shan Ye
Min Zhang
Jing Wu
Hong Yan
Xiaojie Li
Jie He
spellingShingle Zhaoxuan Zhang
Shan Ye
Min Zhang
Jing Wu
Hong Yan
Xiaojie Li
Jie He
High expression of SLC34A2 is a favorable prognostic marker in lung adenocarcinoma patients
Tumor Biology
author_facet Zhaoxuan Zhang
Shan Ye
Min Zhang
Jing Wu
Hong Yan
Xiaojie Li
Jie He
author_sort Zhaoxuan Zhang
title High expression of SLC34A2 is a favorable prognostic marker in lung adenocarcinoma patients
title_short High expression of SLC34A2 is a favorable prognostic marker in lung adenocarcinoma patients
title_full High expression of SLC34A2 is a favorable prognostic marker in lung adenocarcinoma patients
title_fullStr High expression of SLC34A2 is a favorable prognostic marker in lung adenocarcinoma patients
title_full_unstemmed High expression of SLC34A2 is a favorable prognostic marker in lung adenocarcinoma patients
title_sort high expression of slc34a2 is a favorable prognostic marker in lung adenocarcinoma patients
publisher IOS Press
series Tumor Biology
issn 1423-0380
publishDate 2017-07-01
description Dysregulation of SLC34A2 (NaPi2b) in tumors has attracted wide attention, but its expression and function in non–small cell lung cancer remains unclear. By examining its expression in lung adenocarcinoma and correlation to patient outcome, we aimed to explore its prognostic and therapeutic values in this deadly disease. Overall, 175 cases of lung adenocarcinoma sample were included in this study. Histological subtyping of them was diagnosed according to standards of the International Association for the Study of Lung Cancer/American Thoracic Society/European Respiratory Society in 2011. Protein expression of SLC34A2 and anaplastic lymphoma kinase in these samples was determined by immunohistochemistry. Epidermal growth factor receptor mutations were examined using amplification refractory mutation system. Statistical analysis was performed using software of Pearson’s correlation coefficient. High expression of SLC34A2 was identified in about 2/3 patients and correlated with significantly better patient’s overall survival. Epidermal growth factor receptor mutations were detected in about 53% of patients with no statistically significant difference to patient’s overall survival. Anaplastic lymphoma kinase rearrangement was found in 8 out of 175 patients, harboring this abnormality leads to shorter overall survival. No correlation has been found between SLC34A2 expression and epidermal growth factor receptor mutation or anaplastic lymphoma kinase rearrangements in lung adenocarcinoma. High expression of SLC34A2 is present in about 3/4 lung adenocarcinoma samples and predicts better outcome. Since it is a membrane protein, antibody-based drugs targeting this marker might bring new resolution to this deadly disease.
url https://doi.org/10.1177/1010428317720212
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