Dysregulated Expression Profiles of MicroRNAs of Experimentally Induced Cerebral Aneurysms in Rats

Cerebral aneurysm (CA) is an important acquired cerebrovascular disease that can cause catastrophic results. MicroRNAs (miRNAs) are small non-coding RNAs, playing essential roles in modulating basic physiologic and pathological processes. Currently, evidences have been established about biologic rel...

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Published inJournal of Korean Neurosurgical Society Vol. 53; no. 2; pp. 72 - 76
Main Authors Lee, Hyung-Jin, Yi, Jin-Seok, Lee, Hong-Jae, Lee, Il-Woo, Park, Ki-Cheol, Yang, Ji-Ho
Format Journal Article
LanguageEnglish
Published Korea (South) The Korean Neurosurgical Society 01.02.2013
대한신경외과학회
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Online AccessGet full text
ISSN2005-3711
1598-7876
DOI10.3340/jkns.2013.53.2.72

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Abstract Cerebral aneurysm (CA) is an important acquired cerebrovascular disease that can cause catastrophic results. MicroRNAs (miRNAs) are small non-coding RNAs, playing essential roles in modulating basic physiologic and pathological processes. Currently, evidences have been established about biologic relationship between miRNAs and abdominal aortic aneurysms. However, biologic roles of miRNAs in CA formation have not been explained yet. We employed microarray analysis to detect and compare miRNA expression profiles in late stage of CA in rat model. Twenty-six, 7-week-old male Sprague-Dawley rats underwent a CA induction procedure. The control animals (n=11) were fed a normal diet, and the experimental animals (n=26) were fed a normal diet with 1% normal saline for 3 months. Then, the rats were sacrificed, their cerebral arteries were dissected, and the five regions of aneurysmal dilation on the left posterior communicating artery were cut for miRNA microarrays analysis. Six miRNAs (miRNA-1, miRNA-223, miRNA-24-1-5p, miRNA-551b, miRNA-433, and miRNA-489) were randomly chosen for validation using real-time quantitative PCR. Among a set of differentially expressed miRNAs, 14 miRNAs were over-expressed more than 200% and 6 miRNAs were down-expressed lower than 50% in the CA tissues. The results show that miRNAs might take part in CA formation probably by affecting multiple target genes and signaling pathways. Further investigations to identify the exact roles of these miRNAs in CA formation are required.
AbstractList Objective : Cerebral aneurysm (CA) is an important acquired cerebrovascular disease that can cause catastrophic results. MicroRNAs (miRNAs) are small non-coding RNAs, playing essential roles in modulating basic physiologic and pathological processes. Currently, evidences have been established about biologic relationship between miRNAs and abdominal aortic aneurysms. However, biologic roles of miRNAs in CA formation have not been explained yet. We employed microarray analysis to detect and compare miRNA expression profiles in late stage of CA in rat model. Methods : Twenty-six, 7-week-old male Sprague-Dawley rats underwent a CA induction procedure. The control animals (n=11) were fed a normal diet, and the experimental animals (n=26) were fed a normal diet with 1% normal saline for 3 months. Then, the rats were sacrificed, their cerebral arteries were dissected, and the five regions of aneurysmal dilation on the left posterior communicating artery were cut for miRNA microarrays analysis. Six miRNAs (miRNA-1, miRNA-223, miRNA-24-1-5p, miRNA-551b, miRNA-433, and miRNA-489) were randomly chosen for validation using real-time quantitative PCR. Results : Among a set of differentially expressed miRNAs, 14 miRNAs were over-expressed more than 200% and 6 miRNAs were down-expressed lower than 50% in the CA tissues. Conclusion : The results show that miRNAs might take part in CA formation probably by affecting multiple target genes and signaling pathways. Further investigations to identify the exact roles of these miRNAs in CA formation are required. KCI Citation Count: 21
Cerebral aneurysm (CA) is an important acquired cerebrovascular disease that can cause catastrophic results. MicroRNAs (miRNAs) are small non-coding RNAs, playing essential roles in modulating basic physiologic and pathological processes. Currently, evidences have been established about biologic relationship between miRNAs and abdominal aortic aneurysms. However, biologic roles of miRNAs in CA formation have not been explained yet. We employed microarray analysis to detect and compare miRNA expression profiles in late stage of CA in rat model.OBJECTIVECerebral aneurysm (CA) is an important acquired cerebrovascular disease that can cause catastrophic results. MicroRNAs (miRNAs) are small non-coding RNAs, playing essential roles in modulating basic physiologic and pathological processes. Currently, evidences have been established about biologic relationship between miRNAs and abdominal aortic aneurysms. However, biologic roles of miRNAs in CA formation have not been explained yet. We employed microarray analysis to detect and compare miRNA expression profiles in late stage of CA in rat model.Twenty-six, 7-week-old male Sprague-Dawley rats underwent a CA induction procedure. The control animals (n=11) were fed a normal diet, and the experimental animals (n=26) were fed a normal diet with 1% normal saline for 3 months. Then, the rats were sacrificed, their cerebral arteries were dissected, and the five regions of aneurysmal dilation on the left posterior communicating artery were cut for miRNA microarrays analysis. Six miRNAs (miRNA-1, miRNA-223, miRNA-24-1-5p, miRNA-551b, miRNA-433, and miRNA-489) were randomly chosen for validation using real-time quantitative PCR.METHODSTwenty-six, 7-week-old male Sprague-Dawley rats underwent a CA induction procedure. The control animals (n=11) were fed a normal diet, and the experimental animals (n=26) were fed a normal diet with 1% normal saline for 3 months. Then, the rats were sacrificed, their cerebral arteries were dissected, and the five regions of aneurysmal dilation on the left posterior communicating artery were cut for miRNA microarrays analysis. Six miRNAs (miRNA-1, miRNA-223, miRNA-24-1-5p, miRNA-551b, miRNA-433, and miRNA-489) were randomly chosen for validation using real-time quantitative PCR.Among a set of differentially expressed miRNAs, 14 miRNAs were over-expressed more than 200% and 6 miRNAs were down-expressed lower than 50% in the CA tissues.RESULTSAmong a set of differentially expressed miRNAs, 14 miRNAs were over-expressed more than 200% and 6 miRNAs were down-expressed lower than 50% in the CA tissues.The results show that miRNAs might take part in CA formation probably by affecting multiple target genes and signaling pathways. Further investigations to identify the exact roles of these miRNAs in CA formation are required.CONCLUSIONThe results show that miRNAs might take part in CA formation probably by affecting multiple target genes and signaling pathways. Further investigations to identify the exact roles of these miRNAs in CA formation are required.
Cerebral aneurysm (CA) is an important acquired cerebrovascular disease that can cause catastrophic results. MicroRNAs (miRNAs) are small non-coding RNAs, playing essential roles in modulating basic physiologic and pathological processes. Currently, evidences have been established about biologic relationship between miRNAs and abdominal aortic aneurysms. However, biologic roles of miRNAs in CA formation have not been explained yet. We employed microarray analysis to detect and compare miRNA expression profiles in late stage of CA in rat model. Twenty-six, 7-week-old male Sprague-Dawley rats underwent a CA induction procedure. The control animals (n=11) were fed a normal diet, and the experimental animals (n=26) were fed a normal diet with 1% normal saline for 3 months. Then, the rats were sacrificed, their cerebral arteries were dissected, and the five regions of aneurysmal dilation on the left posterior communicating artery were cut for miRNA microarrays analysis. Six miRNAs (miRNA-1, miRNA-223, miRNA-24-1-5p, miRNA-551b, miRNA-433, and miRNA-489) were randomly chosen for validation using real-time quantitative PCR. Among a set of differentially expressed miRNAs, 14 miRNAs were over-expressed more than 200% and 6 miRNAs were down-expressed lower than 50% in the CA tissues. The results show that miRNAs might take part in CA formation probably by affecting multiple target genes and signaling pathways. Further investigations to identify the exact roles of these miRNAs in CA formation are required.
Author Yi, Jin-Seok
Park, Ki-Cheol
Lee, Hong-Jae
Lee, Hyung-Jin
Lee, Il-Woo
Yang, Ji-Ho
AuthorAffiliation 2 Clinical Research Institute, Daejeon St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Daejeon, Korea
1 Department of Neurosurgery, Daejeon St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Daejeon, Korea
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Cites_doi 10.1038/nature10834
10.1161/CIRCULATIONAHA.111.044354
10.1620/tjem.222.187
10.1038/nature06607
10.1007/s00432-011-1114-x
10.1038/emboj.2009.370
10.1161/STROKEAHA.110.590976
10.3340/jkns.2008.44.3.116
10.1161/STROKEAHA.107.481838
10.1126/scitranslmed.3003441
10.1182/blood-2009-03-211938
10.1016/j.jocn.2005.11.018
10.1007/s12013-010-9084-1
10.1016/S0092-8674(04)00045-5
10.1161/CIRCULATIONAHA.111.087817
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Issue 2
Keywords Cell proliferation
Inflammation
Intracranial aneurysm
MicroRNAs
Apoptosis
Language English
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This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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References Aoki (10.3340/jkns.2013.53.2.72_ref2) 2008; 21
Maegdefessel (10.3340/jkns.2013.53.2.72_ref13) 2012; 4
Wang (10.3340/jkns.2013.53.2.72_ref16) 2012; 138
Kanematsu (10.3340/jkns.2013.53.2.72_ref11) 2011; 42
Bartel (10.3340/jkns.2013.53.2.72_ref3) 2004; 116
Johnnidis (10.3340/jkns.2013.53.2.72_ref10) 2008; 451
Chan (10.3340/jkns.2013.53.2.72_ref4) 2010; 29
Mishra (10.3340/jkns.2013.53.2.72_ref14) 2010; 57
Park (10.3340/jkns.2013.53.2.72_ref15) 2008; 44
Zhuang (10.3340/jkns.2013.53.2.72_ref17) 2012; 125
Garzon (10.3340/jkns.2013.53.2.72_ref7) 2009; 114
Liu (10.3340/jkns.2013.53.2.72_ref12) 2010; 222
Aoki (10.3340/jkns.2013.53.2.72_ref1) 2007; 38
Choi (10.3340/jkns.2013.53.2.72_ref6) 2006; 39
Gurha (10.3340/jkns.2013.53.2.72_ref9) 2012; 125
Guo (10.3340/jkns.2013.53.2.72_ref8) 2007; 14
Cheung (10.3340/jkns.2013.53.2.72_ref5) 2012; 482
18360691 - Int J Mol Med. 2008 Apr;21(4):453-9
17430778 - J Clin Neurosci. 2007 Jun;14(6):550-5
22358842 - Nature. 2012 Feb 23;482(7386):524-8
22570371 - Circulation. 2012 Jun 5;125(22):2751-61
22207524 - J Cancer Res Clin Oncol. 2012 Apr;138(4):573-84
18278031 - Nature. 2008 Feb 28;451(7182):1125-9
19096660 - J Korean Neurosurg Soc. 2008 Sep;44(3):116-23
17569872 - Stroke. 2007 Aug;38(8):2337-45
21106959 - Stroke. 2011 Jan;42(1):173-8
20422465 - Cell Biochem Biophys. 2010 Jul;57(2-3):67-76
22580331 - Circulation. 2012 Jun 12;125(23):2892-903
19850741 - Blood. 2009 Dec 17;114(26):5331-41
21030819 - Tohoku J Exp Med. 2010 Nov;222(3):187-93
14744438 - Cell. 2004 Jan 23;116(2):281-97
20019669 - EMBO J. 2010 Feb 3;29(3):559-73
22357537 - Sci Transl Med. 2012 Feb 22;4(122):122ra22
References_xml – volume: 482
  start-page: 524
  year: 2012
  ident: 10.3340/jkns.2013.53.2.72_ref5
  publication-title: Nature
  doi: 10.1038/nature10834
– volume: 125
  start-page: 2751
  year: 2012
  ident: 10.3340/jkns.2013.53.2.72_ref9
  publication-title: Circulation
  doi: 10.1161/CIRCULATIONAHA.111.044354
– volume: 222
  start-page: 187
  year: 2010
  ident: 10.3340/jkns.2013.53.2.72_ref12
  publication-title: Tohoku J Exp Med
  doi: 10.1620/tjem.222.187
– volume: 451
  start-page: 1125
  year: 2008
  ident: 10.3340/jkns.2013.53.2.72_ref10
  publication-title: Nature
  doi: 10.1038/nature06607
– volume: 138
  start-page: 573
  year: 2012
  ident: 10.3340/jkns.2013.53.2.72_ref16
  publication-title: J Cancer Res Clin Oncol
  doi: 10.1007/s00432-011-1114-x
– volume: 21
  start-page: 453
  year: 2008
  ident: 10.3340/jkns.2013.53.2.72_ref2
  publication-title: Int J Mol Med
– volume: 29
  start-page: 559
  year: 2010
  ident: 10.3340/jkns.2013.53.2.72_ref4
  publication-title: EMBO J
  doi: 10.1038/emboj.2009.370
– volume: 42
  start-page: 173
  year: 2011
  ident: 10.3340/jkns.2013.53.2.72_ref11
  publication-title: Stroke
  doi: 10.1161/STROKEAHA.110.590976
– volume: 44
  start-page: 116
  year: 2008
  ident: 10.3340/jkns.2013.53.2.72_ref15
  publication-title: J Korean Neurosurg Soc
  doi: 10.3340/jkns.2008.44.3.116
– volume: 38
  start-page: 2337
  year: 2007
  ident: 10.3340/jkns.2013.53.2.72_ref1
  publication-title: Stroke
  doi: 10.1161/STROKEAHA.107.481838
– volume: 4
  start-page: 122ra22
  year: 2012
  ident: 10.3340/jkns.2013.53.2.72_ref13
  publication-title: Sci Transl Med
  doi: 10.1126/scitranslmed.3003441
– volume: 114
  start-page: 5331
  year: 2009
  ident: 10.3340/jkns.2013.53.2.72_ref7
  publication-title: Blood
  doi: 10.1182/blood-2009-03-211938
– volume: 39
  start-page: 46
  year: 2006
  ident: 10.3340/jkns.2013.53.2.72_ref6
  publication-title: J Korean Neurosurg Soc
– volume: 14
  start-page: 550
  year: 2007
  ident: 10.3340/jkns.2013.53.2.72_ref8
  publication-title: J Clin Neurosci
  doi: 10.1016/j.jocn.2005.11.018
– volume: 57
  start-page: 67
  year: 2010
  ident: 10.3340/jkns.2013.53.2.72_ref14
  publication-title: Cell Biochem Biophys
  doi: 10.1007/s12013-010-9084-1
– volume: 116
  start-page: 281
  year: 2004
  ident: 10.3340/jkns.2013.53.2.72_ref3
  publication-title: Cell
  doi: 10.1016/S0092-8674(04)00045-5
– volume: 125
  start-page: 2892
  year: 2012
  ident: 10.3340/jkns.2013.53.2.72_ref17
  publication-title: Circulation
  doi: 10.1161/CIRCULATIONAHA.111.087817
– reference: 22207524 - J Cancer Res Clin Oncol. 2012 Apr;138(4):573-84
– reference: 22570371 - Circulation. 2012 Jun 5;125(22):2751-61
– reference: 17430778 - J Clin Neurosci. 2007 Jun;14(6):550-5
– reference: 22580331 - Circulation. 2012 Jun 12;125(23):2892-903
– reference: 22357537 - Sci Transl Med. 2012 Feb 22;4(122):122ra22
– reference: 20422465 - Cell Biochem Biophys. 2010 Jul;57(2-3):67-76
– reference: 19850741 - Blood. 2009 Dec 17;114(26):5331-41
– reference: 17569872 - Stroke. 2007 Aug;38(8):2337-45
– reference: 20019669 - EMBO J. 2010 Feb 3;29(3):559-73
– reference: 21106959 - Stroke. 2011 Jan;42(1):173-8
– reference: 21030819 - Tohoku J Exp Med. 2010 Nov;222(3):187-93
– reference: 14744438 - Cell. 2004 Jan 23;116(2):281-97
– reference: 18360691 - Int J Mol Med. 2008 Apr;21(4):453-9
– reference: 22358842 - Nature. 2012 Feb 23;482(7386):524-8
– reference: 19096660 - J Korean Neurosurg Soc. 2008 Sep;44(3):116-23
– reference: 18278031 - Nature. 2008 Feb 28;451(7182):1125-9
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Snippet Cerebral aneurysm (CA) is an important acquired cerebrovascular disease that can cause catastrophic results. MicroRNAs (miRNAs) are small non-coding RNAs,...
Objective : Cerebral aneurysm (CA) is an important acquired cerebrovascular disease that can cause catastrophic results. MicroRNAs (miRNAs) are small...
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신경외과학
Title Dysregulated Expression Profiles of MicroRNAs of Experimentally Induced Cerebral Aneurysms in Rats
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