TY - JOUR
T1 - Extracellular microRNAs and oxidative stress in liver injury
T2 - A systematic mini review
AU - Matsuzaki, Juntaro
AU - Ochiya, Takahiro
N1 - Funding Information:
TO received research grant from Kyowa Medex, Kewpie Corporation, Takeda, Rohto Pharmaceutical Co., Ltd., Japan Atherosclerosis Research Foundation, Inter Stem, and BioMimetics Sympathies. JM has no conflict of interest.
Funding Information:
This study was supported by the "Development of Diagnostic Technology for Detection of miRNA in Body Fluids" grant from the Japan Agency for Medical Research and Development and New Energy and Industrial Technology Development Organization (to TO), and a Grant-in-Aid for Scientific Research C (17K09471, to JM).
Funding Information:
This study was supported by the “Development of Diagnostic Technology for Detection of miRNA in Body Fluids” grant from the Japan Agency for Medical Research and Development and New Energy and Industrial Technology Development Organization (to TO), and a Grant-in-Aid for Scientific Research C (17K09471, to JM).
Publisher Copyright:
© 2018 JCBN.
PY - 2018/7
Y1 - 2018/7
N2 - Recent evidence has suggested that extracelluar microRNAs crucial roles in intercellular communications and are promising as minimally invasive biomarkers for various diseases including cancers. Oxidative stress also plays an essential role in homeostasis and disease development. This systematic review aims to clarify the current evidence on the interaction between oxidative stress and extracellular microRNAs. We identified 32 studies that provided information regarding the association between oxidative stress and extracellular microRNAs: 9 focused on the central nervous system, 11 focused on cardiovascular diseases, and 4 focused on liver injury. Endothelial cell-specific miR-126-3p was the most studied extracellular miRNA associated with oxidative stress. In addition, we highlight some reports that describe the mechanisms of how oxidative stress affects extracellular microRNA profiles in liver injury. In liver injury, the levels of miR-122-5p, miR-192-5p, miR-223-3p, and miR-1224-5p were reported to be elevated in the sera. The release of miR-122-5p, miR-192-5p, and miR-1224-5p from hepatocytes may be attributed to oxidative stress. miR-223-3p could be released from neutrophils and suppress oxidative stress in the liver. Elucidation of the mechanisms of the interaction between extracellular microRNAs and oxidative stress would improve our pathophysiological understanding as well as future medical practice.
AB - Recent evidence has suggested that extracelluar microRNAs crucial roles in intercellular communications and are promising as minimally invasive biomarkers for various diseases including cancers. Oxidative stress also plays an essential role in homeostasis and disease development. This systematic review aims to clarify the current evidence on the interaction between oxidative stress and extracellular microRNAs. We identified 32 studies that provided information regarding the association between oxidative stress and extracellular microRNAs: 9 focused on the central nervous system, 11 focused on cardiovascular diseases, and 4 focused on liver injury. Endothelial cell-specific miR-126-3p was the most studied extracellular miRNA associated with oxidative stress. In addition, we highlight some reports that describe the mechanisms of how oxidative stress affects extracellular microRNA profiles in liver injury. In liver injury, the levels of miR-122-5p, miR-192-5p, miR-223-3p, and miR-1224-5p were reported to be elevated in the sera. The release of miR-122-5p, miR-192-5p, and miR-1224-5p from hepatocytes may be attributed to oxidative stress. miR-223-3p could be released from neutrophils and suppress oxidative stress in the liver. Elucidation of the mechanisms of the interaction between extracellular microRNAs and oxidative stress would improve our pathophysiological understanding as well as future medical practice.
KW - Extracellular vesicle
KW - Liquid biopsy
KW - Liver injury
KW - MicroRNA
UR - http://www.scopus.com/inward/record.url?scp=85049615030&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85049615030&partnerID=8YFLogxK
U2 - 10.3164/jcbn.17-123
DO - 10.3164/jcbn.17-123
M3 - Review article
AN - SCOPUS:85049615030
SN - 0912-0009
VL - 63
SP - 6
EP - 11
JO - Journal of Clinical Biochemistry and Nutrition
JF - Journal of Clinical Biochemistry and Nutrition
IS - 1
ER -