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Long noncoding RNA MALAT1 as a candidate serological biomarker for the diagnosis of non‐small cell lung cancer: A meta‐analysis

BACKGROUND: To investigate the diagnostic efficacy of long noncoding RNA metastasis‐associated in lung adenocarcinoma transcript l (MALAT1) as a candidate serological biomarker for non‐small cell lung cancer (NSCLC). METHODS: Diagnostic studies relevant to circulation long noncoding RNA MALAT1 as a...

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Autores principales: Pan, Jie, Bian, Yuan, Cao, Zhuo, Lei, Limei, Pan, Jiongwei, Huang, Jinwei, Cai, Xiaoping, Lan, Xiang, Zheng, Hao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6997019/
https://www.ncbi.nlm.nih.gov/pubmed/31846184
http://dx.doi.org/10.1111/1759-7714.13265
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author Pan, Jie
Bian, Yuan
Cao, Zhuo
Lei, Limei
Pan, Jiongwei
Huang, Jinwei
Cai, Xiaoping
Lan, Xiang
Zheng, Hao
author_facet Pan, Jie
Bian, Yuan
Cao, Zhuo
Lei, Limei
Pan, Jiongwei
Huang, Jinwei
Cai, Xiaoping
Lan, Xiang
Zheng, Hao
author_sort Pan, Jie
collection PubMed
description BACKGROUND: To investigate the diagnostic efficacy of long noncoding RNA metastasis‐associated in lung adenocarcinoma transcript l (MALAT1) as a candidate serological biomarker for non‐small cell lung cancer (NSCLC). METHODS: Diagnostic studies relevant to circulation long noncoding RNA MALAT1 as a candidate serological biomarker for NSCLC were electronically systematically searched in PubMed, EMBASE, EBSCO and CNKI databases. Suitable studies were included in the meta‐analysis by pooling the diagnostic sensitivity, specificity, positive likelihood ratio (+LR), negative likelihood ratio (−LR), diagnostic odds ratio (DOR) and area under the symmetric ROC curve (AUC) through a random or fixed effects model. Deeks' funnel plot was applied for publication bias evaluation. RESULTS: Six studies with eight datasets were finally included in the meta‐analysis after a systematic search of the databases was performed. The pooled diagnostic sensitivity, specificity, +LR, −LR and DOR were 0.81 (95% CI:0.78–0.84), 0.67 (95% CI:0.63–0.71), 2.61 (95% CI:1.81–3.71), 0.28 (95% CI:0.19–0.43) and 13.73 (95% CI:6.19–30.44), respectively. The pooled area under the ROC curve (AUC) were 0.8663 and 0.8658, respectively by symmetric and asymmetric methods. CONCLUSION: Based on the results of our study, serum long noncoding RNA MALAT1 is a promising biomarker for NSCLC screening. However, due to its low specificity, MALAT1 positive cases need further validation for NSCLC by other diagnostic methods such as radiology, cytology, etc.
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spelling pubmed-69970192020-02-05 Long noncoding RNA MALAT1 as a candidate serological biomarker for the diagnosis of non‐small cell lung cancer: A meta‐analysis Pan, Jie Bian, Yuan Cao, Zhuo Lei, Limei Pan, Jiongwei Huang, Jinwei Cai, Xiaoping Lan, Xiang Zheng, Hao Thorac Cancer Original Articles BACKGROUND: To investigate the diagnostic efficacy of long noncoding RNA metastasis‐associated in lung adenocarcinoma transcript l (MALAT1) as a candidate serological biomarker for non‐small cell lung cancer (NSCLC). METHODS: Diagnostic studies relevant to circulation long noncoding RNA MALAT1 as a candidate serological biomarker for NSCLC were electronically systematically searched in PubMed, EMBASE, EBSCO and CNKI databases. Suitable studies were included in the meta‐analysis by pooling the diagnostic sensitivity, specificity, positive likelihood ratio (+LR), negative likelihood ratio (−LR), diagnostic odds ratio (DOR) and area under the symmetric ROC curve (AUC) through a random or fixed effects model. Deeks' funnel plot was applied for publication bias evaluation. RESULTS: Six studies with eight datasets were finally included in the meta‐analysis after a systematic search of the databases was performed. The pooled diagnostic sensitivity, specificity, +LR, −LR and DOR were 0.81 (95% CI:0.78–0.84), 0.67 (95% CI:0.63–0.71), 2.61 (95% CI:1.81–3.71), 0.28 (95% CI:0.19–0.43) and 13.73 (95% CI:6.19–30.44), respectively. The pooled area under the ROC curve (AUC) were 0.8663 and 0.8658, respectively by symmetric and asymmetric methods. CONCLUSION: Based on the results of our study, serum long noncoding RNA MALAT1 is a promising biomarker for NSCLC screening. However, due to its low specificity, MALAT1 positive cases need further validation for NSCLC by other diagnostic methods such as radiology, cytology, etc. John Wiley & Sons Australia, Ltd 2019-12-17 2020-02 /pmc/articles/PMC6997019/ /pubmed/31846184 http://dx.doi.org/10.1111/1759-7714.13265 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
Pan, Jie
Bian, Yuan
Cao, Zhuo
Lei, Limei
Pan, Jiongwei
Huang, Jinwei
Cai, Xiaoping
Lan, Xiang
Zheng, Hao
Long noncoding RNA MALAT1 as a candidate serological biomarker for the diagnosis of non‐small cell lung cancer: A meta‐analysis
title Long noncoding RNA MALAT1 as a candidate serological biomarker for the diagnosis of non‐small cell lung cancer: A meta‐analysis
title_full Long noncoding RNA MALAT1 as a candidate serological biomarker for the diagnosis of non‐small cell lung cancer: A meta‐analysis
title_fullStr Long noncoding RNA MALAT1 as a candidate serological biomarker for the diagnosis of non‐small cell lung cancer: A meta‐analysis
title_full_unstemmed Long noncoding RNA MALAT1 as a candidate serological biomarker for the diagnosis of non‐small cell lung cancer: A meta‐analysis
title_short Long noncoding RNA MALAT1 as a candidate serological biomarker for the diagnosis of non‐small cell lung cancer: A meta‐analysis
title_sort long noncoding rna malat1 as a candidate serological biomarker for the diagnosis of non‐small cell lung cancer: a meta‐analysis
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6997019/
https://www.ncbi.nlm.nih.gov/pubmed/31846184
http://dx.doi.org/10.1111/1759-7714.13265
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