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Distinct Prognostic Values of Phospholipase C Beta Family Members for Non-Small Cell Lung Carcinoma
BACKGROUND: Non-small cell lung cancer (NSCLC) is a main cause of cancer-related mortality worldwide. The relationships of the phospholipase C beta (PLCB) enzymes, which are encoded by the genes PLCB1, PLCB2, PLCB3, and PLCB4, with NSCLC have not been investigated. Therefore, the aim of the present...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6475572/ https://www.ncbi.nlm.nih.gov/pubmed/31080817 http://dx.doi.org/10.1155/2019/4256524 |
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author | Zhang, Tengfang Song, Xiaowei Liao, Xiwen Wang, Xiangkun Zhu, Guangzhi Yang, Chengkun Xie, Xiaoyong |
author_facet | Zhang, Tengfang Song, Xiaowei Liao, Xiwen Wang, Xiangkun Zhu, Guangzhi Yang, Chengkun Xie, Xiaoyong |
author_sort | Zhang, Tengfang |
collection | PubMed |
description | BACKGROUND: Non-small cell lung cancer (NSCLC) is a main cause of cancer-related mortality worldwide. The relationships of the phospholipase C beta (PLCB) enzymes, which are encoded by the genes PLCB1, PLCB2, PLCB3, and PLCB4, with NSCLC have not been investigated. Therefore, the aim of the present study was to identify any correlations between NSCLC prognosis and the expression patterns of PLCB family members. MATERIALS AND METHODS: The prognostic values of the PLCB gene family members in NSCLC patients were evaluated using the “Kaplan–Meier plotter” database, which includes updated gene expression data and survival information of a total of 1,926 NSCLC patients. The GeneMANIA plugin of Cytoscape software was used to evaluate the relationships of the four PLCB family members at the gene and protein levels. Gene ontology enrichment analysis and KEGG pathway analysis were performed using the Database for Annotation, Visualization, and Integrated Discovery. RESULTS: High mRNA expression levels of PLCB1, PLCB2, and PLCB3 were significantly associated with poor overall survival (OS) of all NSCLC patients and significantly associated with poor prognosis of adenocarcinoma. In contrast, high mRNA expression of PLCB4 was associated with better OS of adenocarcinoma patients. In addition, the expression levels of the PLCB family members were correlated to smoking status, clinical stage, and patient sex but not radiotherapy and chemotherapy outcomes. CONCLUSIONS: PLCB1, PLCB2, PLCB3, and PLCB4 appear to be potential biomarkers for the prognosis of patients with NSCLC. The prognostic values of the PLCB genes require further investigations. |
format | Online Article Text |
id | pubmed-6475572 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-64755722019-05-12 Distinct Prognostic Values of Phospholipase C Beta Family Members for Non-Small Cell Lung Carcinoma Zhang, Tengfang Song, Xiaowei Liao, Xiwen Wang, Xiangkun Zhu, Guangzhi Yang, Chengkun Xie, Xiaoyong Biomed Res Int Research Article BACKGROUND: Non-small cell lung cancer (NSCLC) is a main cause of cancer-related mortality worldwide. The relationships of the phospholipase C beta (PLCB) enzymes, which are encoded by the genes PLCB1, PLCB2, PLCB3, and PLCB4, with NSCLC have not been investigated. Therefore, the aim of the present study was to identify any correlations between NSCLC prognosis and the expression patterns of PLCB family members. MATERIALS AND METHODS: The prognostic values of the PLCB gene family members in NSCLC patients were evaluated using the “Kaplan–Meier plotter” database, which includes updated gene expression data and survival information of a total of 1,926 NSCLC patients. The GeneMANIA plugin of Cytoscape software was used to evaluate the relationships of the four PLCB family members at the gene and protein levels. Gene ontology enrichment analysis and KEGG pathway analysis were performed using the Database for Annotation, Visualization, and Integrated Discovery. RESULTS: High mRNA expression levels of PLCB1, PLCB2, and PLCB3 were significantly associated with poor overall survival (OS) of all NSCLC patients and significantly associated with poor prognosis of adenocarcinoma. In contrast, high mRNA expression of PLCB4 was associated with better OS of adenocarcinoma patients. In addition, the expression levels of the PLCB family members were correlated to smoking status, clinical stage, and patient sex but not radiotherapy and chemotherapy outcomes. CONCLUSIONS: PLCB1, PLCB2, PLCB3, and PLCB4 appear to be potential biomarkers for the prognosis of patients with NSCLC. The prognostic values of the PLCB genes require further investigations. Hindawi 2019-04-07 /pmc/articles/PMC6475572/ /pubmed/31080817 http://dx.doi.org/10.1155/2019/4256524 Text en Copyright © 2019 Tengfang Zhang et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Zhang, Tengfang Song, Xiaowei Liao, Xiwen Wang, Xiangkun Zhu, Guangzhi Yang, Chengkun Xie, Xiaoyong Distinct Prognostic Values of Phospholipase C Beta Family Members for Non-Small Cell Lung Carcinoma |
title | Distinct Prognostic Values of Phospholipase C Beta Family Members for Non-Small Cell Lung Carcinoma |
title_full | Distinct Prognostic Values of Phospholipase C Beta Family Members for Non-Small Cell Lung Carcinoma |
title_fullStr | Distinct Prognostic Values of Phospholipase C Beta Family Members for Non-Small Cell Lung Carcinoma |
title_full_unstemmed | Distinct Prognostic Values of Phospholipase C Beta Family Members for Non-Small Cell Lung Carcinoma |
title_short | Distinct Prognostic Values of Phospholipase C Beta Family Members for Non-Small Cell Lung Carcinoma |
title_sort | distinct prognostic values of phospholipase c beta family members for non-small cell lung carcinoma |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6475572/ https://www.ncbi.nlm.nih.gov/pubmed/31080817 http://dx.doi.org/10.1155/2019/4256524 |
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