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PHLPP2 as a novel metastatic and prognostic biomarker in non‐small cell lung cancer patients
BACKGROUND: PH domain and leucine‐rich repeat protein phosphatase 2 (PHLPP2) has been reported to be a potent tumor suppressor in many human cancers. However, PHLPP2 has not been fully researched as a putative clinical prognostic biomarker of lung cancer. METHODS: The Cancer Genome Atlas (TCGA) and...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons Australia, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6825916/ https://www.ncbi.nlm.nih.gov/pubmed/31571378 http://dx.doi.org/10.1111/1759-7714.13196 |
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author | Wang, Hongmei Gu, Ruixue Tian, Fanglin Liu, Yuechao Fan, Weina Xue, Guiqin Cai, Li Xing, Ying |
author_facet | Wang, Hongmei Gu, Ruixue Tian, Fanglin Liu, Yuechao Fan, Weina Xue, Guiqin Cai, Li Xing, Ying |
author_sort | Wang, Hongmei |
collection | PubMed |
description | BACKGROUND: PH domain and leucine‐rich repeat protein phosphatase 2 (PHLPP2) has been reported to be a potent tumor suppressor in many human cancers. However, PHLPP2 has not been fully researched as a putative clinical prognostic biomarker of lung cancer. METHODS: The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) databases including data on 1383 non‐small cell lung cancer (NSCLC) patients were used to determine PHLPP2 expression. PHLPP2 expression was then examined by immunohistochemistry, and its clinical significance analyzed in 134 NSCLC patients, including 73 patients with adenocarcinoma and 81 with squamous cell carcinoma. RESULTS: We found PHLPP2 expression to be less pronounced in NSCLC tissue samples than that in nontumoral lung tissues according to data taken from TCGA and GEO datasets; this outcome was further validated by immunohistochemistry assay. The low PHLPP2 expression level was found to be associated with the presence of lymph node metastasis (P = 0.003). Importantly, PHLPP2 was found to be an independent indicator of prognosis for overall (hazard ratio [HR] = 0.520, 95% confidence interval [Cl] = 0.327–0.827; P = 0.006) and disease‐free survival (HR = 0.489, 95% Cl = 0.308–0.775; P = 0.002) in patients with surgically‐resected NSCLC by multivariate analysis. CONCLUSION: Taken together, our findings show that PHLPP2 is a robust clinical marker for NSCLC survival and could serve as a potential therapeutic target. |
format | Online Article Text |
id | pubmed-6825916 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley & Sons Australia, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-68259162019-11-07 PHLPP2 as a novel metastatic and prognostic biomarker in non‐small cell lung cancer patients Wang, Hongmei Gu, Ruixue Tian, Fanglin Liu, Yuechao Fan, Weina Xue, Guiqin Cai, Li Xing, Ying Thorac Cancer Original Articles BACKGROUND: PH domain and leucine‐rich repeat protein phosphatase 2 (PHLPP2) has been reported to be a potent tumor suppressor in many human cancers. However, PHLPP2 has not been fully researched as a putative clinical prognostic biomarker of lung cancer. METHODS: The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) databases including data on 1383 non‐small cell lung cancer (NSCLC) patients were used to determine PHLPP2 expression. PHLPP2 expression was then examined by immunohistochemistry, and its clinical significance analyzed in 134 NSCLC patients, including 73 patients with adenocarcinoma and 81 with squamous cell carcinoma. RESULTS: We found PHLPP2 expression to be less pronounced in NSCLC tissue samples than that in nontumoral lung tissues according to data taken from TCGA and GEO datasets; this outcome was further validated by immunohistochemistry assay. The low PHLPP2 expression level was found to be associated with the presence of lymph node metastasis (P = 0.003). Importantly, PHLPP2 was found to be an independent indicator of prognosis for overall (hazard ratio [HR] = 0.520, 95% confidence interval [Cl] = 0.327–0.827; P = 0.006) and disease‐free survival (HR = 0.489, 95% Cl = 0.308–0.775; P = 0.002) in patients with surgically‐resected NSCLC by multivariate analysis. CONCLUSION: Taken together, our findings show that PHLPP2 is a robust clinical marker for NSCLC survival and could serve as a potential therapeutic target. John Wiley & Sons Australia, Ltd 2019-09-30 2019-11 /pmc/articles/PMC6825916/ /pubmed/31571378 http://dx.doi.org/10.1111/1759-7714.13196 Text en © 2019 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 http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Wang, Hongmei Gu, Ruixue Tian, Fanglin Liu, Yuechao Fan, Weina Xue, Guiqin Cai, Li Xing, Ying PHLPP2 as a novel metastatic and prognostic biomarker in non‐small cell lung cancer patients |
title | PHLPP2 as a novel metastatic and prognostic biomarker in non‐small cell lung cancer patients |
title_full | PHLPP2 as a novel metastatic and prognostic biomarker in non‐small cell lung cancer patients |
title_fullStr | PHLPP2 as a novel metastatic and prognostic biomarker in non‐small cell lung cancer patients |
title_full_unstemmed | PHLPP2 as a novel metastatic and prognostic biomarker in non‐small cell lung cancer patients |
title_short | PHLPP2 as a novel metastatic and prognostic biomarker in non‐small cell lung cancer patients |
title_sort | phlpp2 as a novel metastatic and prognostic biomarker in non‐small cell lung cancer patients |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6825916/ https://www.ncbi.nlm.nih.gov/pubmed/31571378 http://dx.doi.org/10.1111/1759-7714.13196 |
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