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Loss of phosphatase and tensin homolog expression correlates with clinicopathological features of non‐small cell lung cancer patients and its impact on survival: A systematic review and meta‐analysis

BACKGROUND: Phosphatase and tensin homolog (PTEN), regarded as a tumor suppressor gene, may act as a prognostic biomarker in human cancers. METHODS: All eligible studies from MEDLINE, Embase, CENTRAL, and the Chinese BioMedical Literature Database to October 2016 were incorporated. Two reviewers ind...

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Autores principales: Zhao, Yongsheng, Zheng, Renyan, Li, Jian, Lin, Feng, Liu, Lunxu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5415467/
https://www.ncbi.nlm.nih.gov/pubmed/28263037
http://dx.doi.org/10.1111/1759-7714.12425
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author Zhao, Yongsheng
Zheng, Renyan
Li, Jian
Lin, Feng
Liu, Lunxu
author_facet Zhao, Yongsheng
Zheng, Renyan
Li, Jian
Lin, Feng
Liu, Lunxu
author_sort Zhao, Yongsheng
collection PubMed
description BACKGROUND: Phosphatase and tensin homolog (PTEN), regarded as a tumor suppressor gene, may act as a prognostic biomarker in human cancers. METHODS: All eligible studies from MEDLINE, Embase, CENTRAL, and the Chinese BioMedical Literature Database to October 2016 were incorporated. Two reviewers independently screened the literature according to inclusion and exclusion criteria, extracted the data, assessed the methodological quality of the included studies, and conducted meta‐analysis. RESULTS: A total of 2486 patients from 19 studies were included. PTEN expression was significantly correlated with gender, smoking history, histology (adenocarcinoma [ADC] vs. squamous cell carcinoma), tumor node metastasis stage (I–II vs. III–IV), N status (N0 vs. N1–N3), and distant metastasis (M0 vs. M1). Loss of PTEN expression was associated with poorer overall survival, but had no significant association with disease‐free survival. Subgroup analysis showed that negative PTEN expression was associated with a poorer outcome in Asian and ADC patients, but not in Western or squamous cell carcinoma patients. CONCLUSION: Loss of PTEN might play an unfavorable prognostic role for overall survival of non‐small cell lung cancer patients, especially Asian or ADC patients.
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spelling pubmed-54154672017-05-04 Loss of phosphatase and tensin homolog expression correlates with clinicopathological features of non‐small cell lung cancer patients and its impact on survival: A systematic review and meta‐analysis Zhao, Yongsheng Zheng, Renyan Li, Jian Lin, Feng Liu, Lunxu Thorac Cancer Original Articles BACKGROUND: Phosphatase and tensin homolog (PTEN), regarded as a tumor suppressor gene, may act as a prognostic biomarker in human cancers. METHODS: All eligible studies from MEDLINE, Embase, CENTRAL, and the Chinese BioMedical Literature Database to October 2016 were incorporated. Two reviewers independently screened the literature according to inclusion and exclusion criteria, extracted the data, assessed the methodological quality of the included studies, and conducted meta‐analysis. RESULTS: A total of 2486 patients from 19 studies were included. PTEN expression was significantly correlated with gender, smoking history, histology (adenocarcinoma [ADC] vs. squamous cell carcinoma), tumor node metastasis stage (I–II vs. III–IV), N status (N0 vs. N1–N3), and distant metastasis (M0 vs. M1). Loss of PTEN expression was associated with poorer overall survival, but had no significant association with disease‐free survival. Subgroup analysis showed that negative PTEN expression was associated with a poorer outcome in Asian and ADC patients, but not in Western or squamous cell carcinoma patients. CONCLUSION: Loss of PTEN might play an unfavorable prognostic role for overall survival of non‐small cell lung cancer patients, especially Asian or ADC patients. John Wiley & Sons Australia, Ltd 2017-03-06 2017-05 /pmc/articles/PMC5415467/ /pubmed/28263037 http://dx.doi.org/10.1111/1759-7714.12425 Text en © 2017 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Zhao, Yongsheng
Zheng, Renyan
Li, Jian
Lin, Feng
Liu, Lunxu
Loss of phosphatase and tensin homolog expression correlates with clinicopathological features of non‐small cell lung cancer patients and its impact on survival: A systematic review and meta‐analysis
title Loss of phosphatase and tensin homolog expression correlates with clinicopathological features of non‐small cell lung cancer patients and its impact on survival: A systematic review and meta‐analysis
title_full Loss of phosphatase and tensin homolog expression correlates with clinicopathological features of non‐small cell lung cancer patients and its impact on survival: A systematic review and meta‐analysis
title_fullStr Loss of phosphatase and tensin homolog expression correlates with clinicopathological features of non‐small cell lung cancer patients and its impact on survival: A systematic review and meta‐analysis
title_full_unstemmed Loss of phosphatase and tensin homolog expression correlates with clinicopathological features of non‐small cell lung cancer patients and its impact on survival: A systematic review and meta‐analysis
title_short Loss of phosphatase and tensin homolog expression correlates with clinicopathological features of non‐small cell lung cancer patients and its impact on survival: A systematic review and meta‐analysis
title_sort loss of phosphatase and tensin homolog expression correlates with clinicopathological features of non‐small cell lung cancer patients and its impact on survival: a systematic review and meta‐analysis
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5415467/
https://www.ncbi.nlm.nih.gov/pubmed/28263037
http://dx.doi.org/10.1111/1759-7714.12425
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