Circulating microRNAs in Alzheimer's disease: the search for novel biomarkers

被引:58
作者
Dorval, Veronique [1 ,2 ]
Nelson, Peter T. [3 ]
Hebert, Sebastien S. [1 ,2 ]
机构
[1] CHU Laval, Ctr Hosp Univ Quebec, Ctr Rech, Quebec City, PQ G1V 4G2, Canada
[2] Univ Laval, Dept Psychiat & Neurosci, Quebec City, PQ, Canada
[3] Univ Kentucky, Sanders Brown Ctr Aging, Lexington, KY 40536 USA
基金
加拿大健康研究院;
关键词
microRNA; Alzheimer's disease; biomarker; diagnosis; mild cognitive impairment; COGNITIVE IMPAIRMENT; TARGETS; PLASMA; BRAIN; MECHANISMS; EXPRESSION; PRECURSOR; COMPLEX; CELLS; BETA;
D O I
10.3389/fnmol.2013.00024
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Alzheimer's disease (AD) is the most common neurodegenerative disease in the elderly. While advancements have been made in understanding the genetic and molecular basis of AD, the clinical diagnosis of AD remains difficult, and post-mortem confirmation is often required. Furthermore, the onset of neurodegeneration precedes clinical symptoms by approximately a decade. Consequently, there is a crucial need for an early and accurate diagnosis of AD, which can potentially lead to strategies that can slow down or stop the progression of neurodegeneration and dementia. Recent advances in the non-coding RNA field have shown that microRNAs (miRNAs) can function as powerful biomarkers in human diseases. Studies are emerging suggesting that circulating miRNAs in the cerebrospinal fluid and blood serum have characteristic changes in AD patients. Whether miRNAs can be used in AD diagnosis, alone or in combination with other AD biomarkers (e.g., amyloid and tau), warrants further investigation.
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收藏
页数:6
相关论文
共 54 条
[1]   MicroRNAs and neurodegeneration: role and impact [J].
Abe, Masashi ;
Bonini, Nancy M. .
TRENDS IN CELL BIOLOGY, 2013, 23 (01) :30-36
[2]  
Alexandrov Peter N, 2012, Int J Biochem Mol Biol, V3, P365
[3]   MicroRNA in Alzheimer's disease: an exploratory study in brain, cerebrospinal fluid and plasma [J].
Bekris, Lynn M. ;
Lutz, Franziska ;
Montine, Thomas J. ;
Yu, Chang En ;
Tsuang, Debby ;
Peskind, Elaine R. ;
Leverenz, James B. .
BIOMARKERS, 2013, 18 (05) :455-466
[4]   A microRNA miR-34a-Regulated Bimodal Switch Targets Notch in Colon Cancer Stem Cells [J].
Bu, Pengcheng ;
Chen, Kai-Yuan ;
Chen, Joyce Huan ;
Wang, Lihua ;
Walters, Jewell ;
Shin, Yong Jun ;
Goerger, Julian P. ;
Sun, Jian ;
Witherspoon, Mavee ;
Rakhilin, Nikolai ;
Li, Jiahe ;
Yang, Herman ;
Milsom, Jeff ;
Lee, Sang ;
Zipfel, Warren ;
Jin, Moonsoo M. ;
Guemues, Zeynep H. ;
Lipkin, Steven M. ;
Shen, Xiling .
CELL STEM CELL, 2013, 12 (05) :602-615
[5]   Widespread microRNA repression by Myc contributes to tumorigenesis [J].
Chang, Tsung-Cheng ;
Yu, Duonan ;
Lee, Yun-Sil ;
Wentzel, Erik A. ;
Arking, Dan E. ;
West, Kristin M. ;
Dang, Chi V. ;
Thomas-Tikhonenko, Andrei ;
Mendell, Joshua T. .
NATURE GENETICS, 2008, 40 (01) :43-50
[6]  
Chintamaneni Meena, 2012, ISRN Pharmacol, V2012, P984786, DOI 10.5402/2012/984786
[7]   Identification of miRNA changes in Alzheimer's disease brain and CSF yields putative biomarkers and insights into disease pathways [J].
Cogswell, John P. ;
Ward, James ;
Taylor, Ian A. ;
Waters, Michelle ;
Shi, Yunling ;
Cannon, Brian ;
Kelnar, Kevin ;
Kemppainen, Jon ;
Brown, David ;
Chen, Caifu ;
Prinjha, Rab K. ;
Richardson, Jill C. ;
Saunders, Ann M. ;
Roses, Allen D. ;
Richards, Cynthia A. .
JOURNAL OF ALZHEIMERS DISEASE, 2008, 14 (01) :27-41
[8]   A functional screen identifies miR-34a as a candidate neuroblastoma tumor suppressor gene [J].
Cole, Kristina A. ;
Attiyeh, Edward F. ;
Mosse, Yael P. ;
Laquaglia, Michael J. ;
Diskin, Sharon J. ;
Brodeur, Garrett M. ;
Maris, John M. .
MOLECULAR CANCER RESEARCH, 2008, 6 (05) :735-742
[9]   MicroRNAs in Alzheimer's disease [J].
Delay, Charlotte ;
Mandemakers, Wim ;
Hebert, Sebastien S. .
NEUROBIOLOGY OF DISEASE, 2012, 46 (02) :285-290
[10]   Gene Network and Pathway Analysis of Mice with Conditional Ablation of Dicer in Post-Mitotic Neurons [J].
Dorval, Veronique ;
Smith, Pascal Y. ;
Delay, Charlotte ;
Calvo, Ezequiel ;
Planel, Emmanuel ;
Zommer, Nadege ;
Buee, Luc ;
Hebert, Sebastien S. .
PLOS ONE, 2012, 7 (08)