A Molecular Signature of Two Long Non-Coding RNAs in Peripheral Blood Predicts Acute Renal Allograft Rejection

Background/Aims: Acute rejection (AR) is a major complication post renal transplantation, with no widely-accepted non-invasive biomarker. This study aimed to explore the expression profiles of long non-coding RNAs (lncRNAs) in the peripheral blood (PB) of renal transplant recipients and their potent...

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Main Authors: Yu-Zheng Ge, Tao Xu, Wei-Jun Cao, Ran Wu, Wen-Tao Yao, Chang-Cheng Zhou, Min Wang, Lu-Wei Xu, Tian-Ze Lu, You-Cai Zhao, Zhi-Kai Hu, Zhong-Le Xu, Xiao-Bing Yang, Liu-Hua Zhou, Sheng-Li Zhang, Bing Zhong, Zheng Xu, Wen-Cheng Li, Jia-Geng Zhu, Rui-Peng Jia
Format: Article
Language:English
Published: Cell Physiol Biochem Press GmbH & Co KG 2017-11-01
Series:Cellular Physiology and Biochemistry
Subjects:
Online Access:https://www.karger.com/Article/FullText/485451
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author Yu-Zheng Ge
Tao Xu
Wei-Jun Cao
Ran Wu
Wen-Tao Yao
Chang-Cheng Zhou
Min Wang
Lu-Wei Xu
Tian-Ze Lu
You-Cai Zhao
Zhi-Kai Hu
Zhong-Le Xu
Xiao-Bing Yang
Liu-Hua Zhou
Sheng-Li Zhang
Bing Zhong
Zheng Xu
Wen-Cheng Li
Jia-Geng Zhu
Rui-Peng Jia
author_facet Yu-Zheng Ge
Tao Xu
Wei-Jun Cao
Ran Wu
Wen-Tao Yao
Chang-Cheng Zhou
Min Wang
Lu-Wei Xu
Tian-Ze Lu
You-Cai Zhao
Zhi-Kai Hu
Zhong-Le Xu
Xiao-Bing Yang
Liu-Hua Zhou
Sheng-Li Zhang
Bing Zhong
Zheng Xu
Wen-Cheng Li
Jia-Geng Zhu
Rui-Peng Jia
author_sort Yu-Zheng Ge
collection DOAJ
description Background/Aims: Acute rejection (AR) is a major complication post renal transplantation, with no widely-accepted non-invasive biomarker. This study aimed to explore the expression profiles of long non-coding RNAs (lncRNAs) in the peripheral blood (PB) of renal transplant recipients and their potential diagnostic values. Methods: The genome-wide lncRNA expression profiles were analyzed in 150 PB samples from pediatric and adult renal transplant (PRTx and ARTx) cohorts. The diagnostic performance of differentially expressed lncRNA was determined using receiver operator characteristic curve, with area under the curve (AUC) and 95% confidential interval (CI). Finally, a risk score was constructed with logistical regression model. Results: A total of 162 lncRNAs were found differentially expressed in PRTx cohort, while 163 in ARTx cohort. Among these identified lncRNAs, 23 deregulated accordingly in both cohorts, and could distinguish AR recipients from those without AR. Finally, a risk score with two most significant lncRNAs (AF264622 and AB209021) was generated and exhibited excellent diagnostic performance in both PRTx (AUC:0.829, 95% CI:0.735-0.922) and ARTx cohorts (AUC: 0.889, 95% CI: 0.817-0.960). Conclusion: A molecular signature of two lncRNAs in PB could serve as a novel non-invasive biomarker for the diagnosis of AR in both pediatric and adult renal transplant recipients.
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spelling doaj.art-33ffc787940341cd91a7bbf20c02d9182022-12-21T18:30:44ZengCell Physiol Biochem Press GmbH & Co KGCellular Physiology and Biochemistry1015-89871421-97782017-11-014431213122310.1159/000485451485451A Molecular Signature of Two Long Non-Coding RNAs in Peripheral Blood Predicts Acute Renal Allograft RejectionYu-Zheng GeTao XuWei-Jun CaoRan WuWen-Tao YaoChang-Cheng ZhouMin WangLu-Wei XuTian-Ze LuYou-Cai ZhaoZhi-Kai HuZhong-Le XuXiao-Bing YangLiu-Hua ZhouSheng-Li ZhangBing ZhongZheng XuWen-Cheng LiJia-Geng ZhuRui-Peng JiaBackground/Aims: Acute rejection (AR) is a major complication post renal transplantation, with no widely-accepted non-invasive biomarker. This study aimed to explore the expression profiles of long non-coding RNAs (lncRNAs) in the peripheral blood (PB) of renal transplant recipients and their potential diagnostic values. Methods: The genome-wide lncRNA expression profiles were analyzed in 150 PB samples from pediatric and adult renal transplant (PRTx and ARTx) cohorts. The diagnostic performance of differentially expressed lncRNA was determined using receiver operator characteristic curve, with area under the curve (AUC) and 95% confidential interval (CI). Finally, a risk score was constructed with logistical regression model. Results: A total of 162 lncRNAs were found differentially expressed in PRTx cohort, while 163 in ARTx cohort. Among these identified lncRNAs, 23 deregulated accordingly in both cohorts, and could distinguish AR recipients from those without AR. Finally, a risk score with two most significant lncRNAs (AF264622 and AB209021) was generated and exhibited excellent diagnostic performance in both PRTx (AUC:0.829, 95% CI:0.735-0.922) and ARTx cohorts (AUC: 0.889, 95% CI: 0.817-0.960). Conclusion: A molecular signature of two lncRNAs in PB could serve as a novel non-invasive biomarker for the diagnosis of AR in both pediatric and adult renal transplant recipients.https://www.karger.com/Article/FullText/485451Renal transplantAcute rejectionLong non-coding RNADiagnosisBiomarker
spellingShingle Yu-Zheng Ge
Tao Xu
Wei-Jun Cao
Ran Wu
Wen-Tao Yao
Chang-Cheng Zhou
Min Wang
Lu-Wei Xu
Tian-Ze Lu
You-Cai Zhao
Zhi-Kai Hu
Zhong-Le Xu
Xiao-Bing Yang
Liu-Hua Zhou
Sheng-Li Zhang
Bing Zhong
Zheng Xu
Wen-Cheng Li
Jia-Geng Zhu
Rui-Peng Jia
A Molecular Signature of Two Long Non-Coding RNAs in Peripheral Blood Predicts Acute Renal Allograft Rejection
Cellular Physiology and Biochemistry
Renal transplant
Acute rejection
Long non-coding RNA
Diagnosis
Biomarker
title A Molecular Signature of Two Long Non-Coding RNAs in Peripheral Blood Predicts Acute Renal Allograft Rejection
title_full A Molecular Signature of Two Long Non-Coding RNAs in Peripheral Blood Predicts Acute Renal Allograft Rejection
title_fullStr A Molecular Signature of Two Long Non-Coding RNAs in Peripheral Blood Predicts Acute Renal Allograft Rejection
title_full_unstemmed A Molecular Signature of Two Long Non-Coding RNAs in Peripheral Blood Predicts Acute Renal Allograft Rejection
title_short A Molecular Signature of Two Long Non-Coding RNAs in Peripheral Blood Predicts Acute Renal Allograft Rejection
title_sort molecular signature of two long non coding rnas in peripheral blood predicts acute renal allograft rejection
topic Renal transplant
Acute rejection
Long non-coding RNA
Diagnosis
Biomarker
url https://www.karger.com/Article/FullText/485451
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