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LncRNA-NEF is downregulated in postmenopausal osteoporosis and is related to course of treatment and recurrence

OBJECTIVES: We investigated the role of long non-coding (lnc) RNA-NEF (neighboring enhancer of FoxA2), a characterized oncogene in cancer biology, in postmenopausal osteoporosis and its diagnostic and prognostic value in this disease. METHODS: Expression of lncRNA-NEF in plasma was detected by RNA e...

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Autores principales: Ma, Xiaoyong, Guo, Zhixue, Gao, Wenshan, Wang, Jianzhong, Liu, Yong, Gao, Fei, Sun, Shaosong, Zhou, Xiaozhe, Yang, Zhaoyu, Zheng, Wenkui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6683934/
https://www.ncbi.nlm.nih.gov/pubmed/31220986
http://dx.doi.org/10.1177/0300060519847854
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author Ma, Xiaoyong
Guo, Zhixue
Gao, Wenshan
Wang, Jianzhong
Liu, Yong
Gao, Fei
Sun, Shaosong
Zhou, Xiaozhe
Yang, Zhaoyu
Zheng, Wenkui
author_facet Ma, Xiaoyong
Guo, Zhixue
Gao, Wenshan
Wang, Jianzhong
Liu, Yong
Gao, Fei
Sun, Shaosong
Zhou, Xiaozhe
Yang, Zhaoyu
Zheng, Wenkui
author_sort Ma, Xiaoyong
collection PubMed
description OBJECTIVES: We investigated the role of long non-coding (lnc) RNA-NEF (neighboring enhancer of FoxA2), a characterized oncogene in cancer biology, in postmenopausal osteoporosis and its diagnostic and prognostic value in this disease. METHODS: Expression of lncRNA-NEF in plasma was detected by RNA extraction and real-time quantitative PCR. The diagnostic value of lncRNA-NEF and interleukin (IL)-6 for postmenopausal osteoporosis was evaluated by receiver operating characteristic curve analysis, with postmenopausal osteoporosis patients as true positive cases and healthy volunteers as true negative cases. RESULTS: We showed that plasma lncRNA-NEF was downregulated and plasma IL-6 was upregulated in postmenopausal osteoporosis patients compared with healthy controls. Altered plasma levels of lncRNA-NEF and IL-6 separated postmenopausal osteoporosis patients from healthy controls, and lncRNA-NEF and IL-6 were inversely and significantly correlated in osteoporosis patients. Patients were divided into high (n = 68) and low lncRNA-NEF (n = 73) groups according to Youden’s index. Patients with high lncRNA-NEF levels required a significantly shorter treatment course and had a lower post-treatment recurrence rate. CONCLUSION: We showed that lncRNA-NEF is downregulated in postmenopausal osteoporosis and is related to course of treatment and recurrence. The involvement of lncRNA-NEF in postmenopausal osteoporosis is likely related to IL-6.
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spelling pubmed-66839342019-08-19 LncRNA-NEF is downregulated in postmenopausal osteoporosis and is related to course of treatment and recurrence Ma, Xiaoyong Guo, Zhixue Gao, Wenshan Wang, Jianzhong Liu, Yong Gao, Fei Sun, Shaosong Zhou, Xiaozhe Yang, Zhaoyu Zheng, Wenkui J Int Med Res Pre-Clinical Research Reports OBJECTIVES: We investigated the role of long non-coding (lnc) RNA-NEF (neighboring enhancer of FoxA2), a characterized oncogene in cancer biology, in postmenopausal osteoporosis and its diagnostic and prognostic value in this disease. METHODS: Expression of lncRNA-NEF in plasma was detected by RNA extraction and real-time quantitative PCR. The diagnostic value of lncRNA-NEF and interleukin (IL)-6 for postmenopausal osteoporosis was evaluated by receiver operating characteristic curve analysis, with postmenopausal osteoporosis patients as true positive cases and healthy volunteers as true negative cases. RESULTS: We showed that plasma lncRNA-NEF was downregulated and plasma IL-6 was upregulated in postmenopausal osteoporosis patients compared with healthy controls. Altered plasma levels of lncRNA-NEF and IL-6 separated postmenopausal osteoporosis patients from healthy controls, and lncRNA-NEF and IL-6 were inversely and significantly correlated in osteoporosis patients. Patients were divided into high (n = 68) and low lncRNA-NEF (n = 73) groups according to Youden’s index. Patients with high lncRNA-NEF levels required a significantly shorter treatment course and had a lower post-treatment recurrence rate. CONCLUSION: We showed that lncRNA-NEF is downregulated in postmenopausal osteoporosis and is related to course of treatment and recurrence. The involvement of lncRNA-NEF in postmenopausal osteoporosis is likely related to IL-6. SAGE Publications 2019-06-20 2019-07 /pmc/articles/PMC6683934/ /pubmed/31220986 http://dx.doi.org/10.1177/0300060519847854 Text en © The Author(s) 2019 http://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Pre-Clinical Research Reports
Ma, Xiaoyong
Guo, Zhixue
Gao, Wenshan
Wang, Jianzhong
Liu, Yong
Gao, Fei
Sun, Shaosong
Zhou, Xiaozhe
Yang, Zhaoyu
Zheng, Wenkui
LncRNA-NEF is downregulated in postmenopausal osteoporosis and is related to course of treatment and recurrence
title LncRNA-NEF is downregulated in postmenopausal osteoporosis and is related to course of treatment and recurrence
title_full LncRNA-NEF is downregulated in postmenopausal osteoporosis and is related to course of treatment and recurrence
title_fullStr LncRNA-NEF is downregulated in postmenopausal osteoporosis and is related to course of treatment and recurrence
title_full_unstemmed LncRNA-NEF is downregulated in postmenopausal osteoporosis and is related to course of treatment and recurrence
title_short LncRNA-NEF is downregulated in postmenopausal osteoporosis and is related to course of treatment and recurrence
title_sort lncrna-nef is downregulated in postmenopausal osteoporosis and is related to course of treatment and recurrence
topic Pre-Clinical Research Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6683934/
https://www.ncbi.nlm.nih.gov/pubmed/31220986
http://dx.doi.org/10.1177/0300060519847854
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