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Expression patterns and clinical significances of ENO2 in lung cancer: an analysis based on Oncomine database

BACKGROUND: Lung cancer is a heterogeneous malignant tumor involving more than 50 histological subtypes. Currently, molecularly targeted drugs have been shown to have promising applications in the clinical treatment of lung cancer. This study aims to explore the expression patterns and prognostic po...

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Autores principales: Liu, Desen, Mao, Yiming, Chen, Cheng, Zhu, Feng, Lu, Wenqiang, Ma, Haitao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7290642/
https://www.ncbi.nlm.nih.gov/pubmed/32566576
http://dx.doi.org/10.21037/atm-20-3354
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author Liu, Desen
Mao, Yiming
Chen, Cheng
Zhu, Feng
Lu, Wenqiang
Ma, Haitao
author_facet Liu, Desen
Mao, Yiming
Chen, Cheng
Zhu, Feng
Lu, Wenqiang
Ma, Haitao
author_sort Liu, Desen
collection PubMed
description BACKGROUND: Lung cancer is a heterogeneous malignant tumor involving more than 50 histological subtypes. Currently, molecularly targeted drugs have been shown to have promising applications in the clinical treatment of lung cancer. This study aims to explore the expression patterns and prognostic potential of enolase 2 (ENO2) in lung cancer. METHODS: Differential expressions of ENO2 in lung cancer cases were analyzed using the Oncomine database. Meanwhile, the prognostic potentials of ENO2 in lung cancer were assessed by deploying the Kaplan-Meier plotter database. RESULTS: Forty-one studies reported a significant difference in ENO2 expression between tumors and the normal healthy control tissues. Among all the studies, there was an upregulation of ENO2 in 29 studies, and downregulation in 12 studies. 9/41 studies revealed upregulated ENO2 in distinct types of tumor tissues, including cervical cancer, esophageal cancer, kidney cancer, leukemia, melanoma, pancreatic cancer, sarcoma, and lung cancer. Furthermore, upregulated ENO2 was identified in 365 cases of lung cancer (P<0.05). By analyzing the Kaplan-Meier Plotter database, the ENO2 level was negatively correlated to the overall survival of lung cancer patients (P<0.05). Subsequently, subgroup analysis revealed that the prognostic potential of ENO2 was much more pronounced in lung adenocarcinoma patients (P<0.05). CONCLUSIONS: ENO2 is upregulated in lung cancer tissues and linked to the prognosis. It can be used as a therapeutic target for developing lung cancer drugs.
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spelling pubmed-72906422020-06-19 Expression patterns and clinical significances of ENO2 in lung cancer: an analysis based on Oncomine database Liu, Desen Mao, Yiming Chen, Cheng Zhu, Feng Lu, Wenqiang Ma, Haitao Ann Transl Med Original Article BACKGROUND: Lung cancer is a heterogeneous malignant tumor involving more than 50 histological subtypes. Currently, molecularly targeted drugs have been shown to have promising applications in the clinical treatment of lung cancer. This study aims to explore the expression patterns and prognostic potential of enolase 2 (ENO2) in lung cancer. METHODS: Differential expressions of ENO2 in lung cancer cases were analyzed using the Oncomine database. Meanwhile, the prognostic potentials of ENO2 in lung cancer were assessed by deploying the Kaplan-Meier plotter database. RESULTS: Forty-one studies reported a significant difference in ENO2 expression between tumors and the normal healthy control tissues. Among all the studies, there was an upregulation of ENO2 in 29 studies, and downregulation in 12 studies. 9/41 studies revealed upregulated ENO2 in distinct types of tumor tissues, including cervical cancer, esophageal cancer, kidney cancer, leukemia, melanoma, pancreatic cancer, sarcoma, and lung cancer. Furthermore, upregulated ENO2 was identified in 365 cases of lung cancer (P<0.05). By analyzing the Kaplan-Meier Plotter database, the ENO2 level was negatively correlated to the overall survival of lung cancer patients (P<0.05). Subsequently, subgroup analysis revealed that the prognostic potential of ENO2 was much more pronounced in lung adenocarcinoma patients (P<0.05). CONCLUSIONS: ENO2 is upregulated in lung cancer tissues and linked to the prognosis. It can be used as a therapeutic target for developing lung cancer drugs. AME Publishing Company 2020-05 /pmc/articles/PMC7290642/ /pubmed/32566576 http://dx.doi.org/10.21037/atm-20-3354 Text en 2020 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Liu, Desen
Mao, Yiming
Chen, Cheng
Zhu, Feng
Lu, Wenqiang
Ma, Haitao
Expression patterns and clinical significances of ENO2 in lung cancer: an analysis based on Oncomine database
title Expression patterns and clinical significances of ENO2 in lung cancer: an analysis based on Oncomine database
title_full Expression patterns and clinical significances of ENO2 in lung cancer: an analysis based on Oncomine database
title_fullStr Expression patterns and clinical significances of ENO2 in lung cancer: an analysis based on Oncomine database
title_full_unstemmed Expression patterns and clinical significances of ENO2 in lung cancer: an analysis based on Oncomine database
title_short Expression patterns and clinical significances of ENO2 in lung cancer: an analysis based on Oncomine database
title_sort expression patterns and clinical significances of eno2 in lung cancer: an analysis based on oncomine database
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7290642/
https://www.ncbi.nlm.nih.gov/pubmed/32566576
http://dx.doi.org/10.21037/atm-20-3354
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