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MicroRNA-200b expression level is negatively associated with pathological grading in human gliomas

AIM: To elucidate the clinical implication of microRNA (miRNA)-200b in the pathological grading of gliomas. METHODS: We searched the Chinese National Knowledge Infrastructure, Web of Knowledge, Embase, and PubMed databases. Related articles were assessed, and ORs with 95% CIs were calculated to exam...

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Autores principales: Kong, Xiangyi, Gong, Shun, Yan, Tao, Yang, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6112773/
https://www.ncbi.nlm.nih.gov/pubmed/30197535
http://dx.doi.org/10.2147/CMAR.S171137
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author Kong, Xiangyi
Gong, Shun
Yan, Tao
Yang, Yi
author_facet Kong, Xiangyi
Gong, Shun
Yan, Tao
Yang, Yi
author_sort Kong, Xiangyi
collection PubMed
description AIM: To elucidate the clinical implication of microRNA (miRNA)-200b in the pathological grading of gliomas. METHODS: We searched the Chinese National Knowledge Infrastructure, Web of Knowledge, Embase, and PubMed databases. Related articles were assessed, and ORs with 95% CIs were calculated to examine the relationship between miRNA-200b expression levels and the World Health Organization (WHO) glioma grade, patients’ sex and age, tumor size, and extent of surgical resection. Heterogeneity, publication bias, and stability of the pooled results of the included studies were also analyzed. MiR-200b expression in 87 human glioma tissues (50 high grade and 37 low grade) and matched 41 non-neoplastic brain tissues was measured by real-time quantitative RT-PCR assay. RESULTS: Five eligible studies involving 630 patients were included in the present meta-analysis. The miRNA-200b expression in glioma tissues was negatively associated with the WHO glioma grade (OR, 0.070; 95% CI, 0.007–0.678; P=0.022). No significant correlations were found between miRNA-200b and sex (P=0.858), age (P=0.776), tumor size (P=0.134), or extent of resection (P=0.778). In our own test, compared with non-neoplastic brain tissues, the expression level of miR-200b was significantly decreased in glioma tissues (tumor vs normal: 4.29±1.90 vs 10.45±2.34, P<0.001). In addition, we found that the glioma tissues from high-grade tumors (grade III and IV) had much lower miR-200b expression than glioma tissues from low grade tumors (grade I and II). CONCLUSION: Our results suggest that the miRNA-200 expression level may be negatively associated with the WHO glioma grade (malignancy). MiRNA-200 might serve as a prognostic and diagnostic biomarker or a helpful therapeutic target.
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spelling pubmed-61127732018-09-07 MicroRNA-200b expression level is negatively associated with pathological grading in human gliomas Kong, Xiangyi Gong, Shun Yan, Tao Yang, Yi Cancer Manag Res Original Research AIM: To elucidate the clinical implication of microRNA (miRNA)-200b in the pathological grading of gliomas. METHODS: We searched the Chinese National Knowledge Infrastructure, Web of Knowledge, Embase, and PubMed databases. Related articles were assessed, and ORs with 95% CIs were calculated to examine the relationship between miRNA-200b expression levels and the World Health Organization (WHO) glioma grade, patients’ sex and age, tumor size, and extent of surgical resection. Heterogeneity, publication bias, and stability of the pooled results of the included studies were also analyzed. MiR-200b expression in 87 human glioma tissues (50 high grade and 37 low grade) and matched 41 non-neoplastic brain tissues was measured by real-time quantitative RT-PCR assay. RESULTS: Five eligible studies involving 630 patients were included in the present meta-analysis. The miRNA-200b expression in glioma tissues was negatively associated with the WHO glioma grade (OR, 0.070; 95% CI, 0.007–0.678; P=0.022). No significant correlations were found between miRNA-200b and sex (P=0.858), age (P=0.776), tumor size (P=0.134), or extent of resection (P=0.778). In our own test, compared with non-neoplastic brain tissues, the expression level of miR-200b was significantly decreased in glioma tissues (tumor vs normal: 4.29±1.90 vs 10.45±2.34, P<0.001). In addition, we found that the glioma tissues from high-grade tumors (grade III and IV) had much lower miR-200b expression than glioma tissues from low grade tumors (grade I and II). CONCLUSION: Our results suggest that the miRNA-200 expression level may be negatively associated with the WHO glioma grade (malignancy). MiRNA-200 might serve as a prognostic and diagnostic biomarker or a helpful therapeutic target. Dove Medical Press 2018-08-24 /pmc/articles/PMC6112773/ /pubmed/30197535 http://dx.doi.org/10.2147/CMAR.S171137 Text en © 2018 Kong et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Kong, Xiangyi
Gong, Shun
Yan, Tao
Yang, Yi
MicroRNA-200b expression level is negatively associated with pathological grading in human gliomas
title MicroRNA-200b expression level is negatively associated with pathological grading in human gliomas
title_full MicroRNA-200b expression level is negatively associated with pathological grading in human gliomas
title_fullStr MicroRNA-200b expression level is negatively associated with pathological grading in human gliomas
title_full_unstemmed MicroRNA-200b expression level is negatively associated with pathological grading in human gliomas
title_short MicroRNA-200b expression level is negatively associated with pathological grading in human gliomas
title_sort microrna-200b expression level is negatively associated with pathological grading in human gliomas
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6112773/
https://www.ncbi.nlm.nih.gov/pubmed/30197535
http://dx.doi.org/10.2147/CMAR.S171137
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