4.2 Article

Microarray Analysis of Long Noncoding RNAs in Female Diabetic Peripheral Neuropathy Patients

期刊

CELLULAR PHYSIOLOGY AND BIOCHEMISTRY
卷 46, 期 3, 页码 1209-1217

出版社

KARGER
DOI: 10.1159/000489071

关键词

Diabetic peripheral neuropathy; Long noncoding RNA; MAPK signaling pathway; Coexpression network

资金

  1. Applied Research Project on Nonprofit Technology of Zhejiang Province [2015C33309]
  2. National Natural Science Foundation of China [81541039, 81402747]
  3. Natural Science Foundation of Ningbo [2016A610085, 2017A610199]
  4. K.C. Wong Magna Fund in Ningbo University

向作者/读者索取更多资源

Background/Aims: Diabetic peripheral neuropathy (DPN) is the most common complication of diabetes mellitus (DM). Because of its controversial pathogenesis, DPN is still not diagnosed or managed properly in most patients. Methods: In this study, human lncRNA microarrays were used to identify the differentially expressed lncRNAs in DM and DPN patients, and some of the discovered lncRNAs were further validated in additional 78 samples by quantitative realtime PCR (qRT-PCR). Results: The microarray analysis identified 446 and 1327 differentially expressed lncRNAs in DM and DPN, respectively. The KEGG pathway analysis further revealed that the differentially expressed lncRNA-coexpressed mRNAs between DPN and DM groups were significantly enriched in the MAPK signaling pathway. The lncRNA/mRNA coexpression network indicated that BDNF and TRAF2 correlated with 6 lncRNAs. The qRT-PCR confirmed the initial microarray results. Conclusion: These findings demonstrated that the interplay between lncRNAs and mRNA may be involved in the pathogenesis of DPN, especially the neurotrophin-MAPK signaling pathway, thus providing relevant information for future studies. (C) 2018 The Author(s) Published by S. Karger AG, Basel

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