机构:[1]Chinese Univ Hong Kong, Li Ka Shing Inst Hlth Sci, Shatin, Hong Kong, Peoples R China[2]Chinese Univ Hong Kong, Dept Chem Pathol, Hong Kong, Hong Kong, Peoples R China[3]First Peoples Hosp Yunnan Prov, Dept Nephrol, Xinjiang, Yunnan, Peoples R China内科片肾内科云南省第一人民医院[4]Chinese Univ Hong Kong, Shenzhen Res Inst, Shenzhen, Peoples R China[5]Sun Yat Sen Univ, Affiliated Hosp 1, Dept Nephrol, Guangzhou 510275, Guangdong, Peoples R China中山大学附属第一医院[6]Chinese Univ Hong Kong, Dept Med & Therapeut, Hong Kong, Hong Kong, Peoples R China
Rapid growth of diabetes and diabetic kidney disease exerts a great burden on society. Owing to the lack of effective treatments for diabetic kidney disease, treatment relies on drugs that either reduces its progression or involve renal replacement therapies, such as dialysis and kidney transplantation. It is urgent to search for biomarkers for early diagnosis and effective therapy. The discovery of microRNAs had lead to a new era of post-transcriptional regulators of gene expression. Studies from cells, experimental animal models and patients under diabetic conditions demonstrate that expression patterns of microRNAs are altered during the progression of diabetic kidney disease. Functional studies indicate that the ability of microRNAs to bind 3 ' untranslated region of messenger RNA not only shows their capability to regulate expression of target genes, but also their therapeutic potential to diabetic kidney disease. The presence of microRNAs in plasma, serum, and urine has been shown to be possible biomarkers in diabetic kidney disease. Therefore, identification of the pathogenic role of microRNAs possesses an important clinical impact in terms of prevention and treatment of progression in diabetic kidney disease because it allows us to design novel and specific therapies and diagnostic tools for diabetic kidney disease.
基金:
Major State Basic
Research Development Program of China (973 Program, no.
2012CB517700 to Hui Y. Lan) and National Natural Science
Foundation of China (General Program 81170681 to Arthur
C. Chung and Key Program 81130012 to Xueqing Yu); the
Research Grant Council of Hong Kong (RGC GRF 468711,
469110, CUHK5/CRF/09 toHui Y. Lan.; GRF 463612, 464010,
763908, and 764109 to Arthur C. Chung); the Focused
Investment Scheme A and B and direct Grants from the
Chinese University of Hong Kong (2011.1.076, 2012.1.021 to
Arthur C. Chung); 2011 Research Grant from Hong Kong
Society of Nephrology (6903213 to Arthur C. Chung); and
Municipal Science and Technology R&D funding of basic
research, Shenzhen (Major Program JC201104220290A to
Hui Y. Lan and General ProgramJC201105201059A to Arthur
C. Chung). Project support for national and provincial funding
from Shenzhen city (GJHS20120702105523297 to Arthur
C. Chung).
第一作者机构:[1]Chinese Univ Hong Kong, Li Ka Shing Inst Hlth Sci, Shatin, Hong Kong, Peoples R China[2]Chinese Univ Hong Kong, Dept Chem Pathol, Hong Kong, Hong Kong, Peoples R China[3]First Peoples Hosp Yunnan Prov, Dept Nephrol, Xinjiang, Yunnan, Peoples R China
通讯作者:
通讯机构:[1]Chinese Univ Hong Kong, Li Ka Shing Inst Hlth Sci, Shatin, Hong Kong, Peoples R China[4]Chinese Univ Hong Kong, Shenzhen Res Inst, Shenzhen, Peoples R China
推荐引用方式(GB/T 7714):
Li Rong,Chung Arthur C. K.,Yu Xueqing,et al.MicroRNAs in Diabetic Kidney Disease[J].INTERNATIONAL JOURNAL OF ENDOCRINOLOGY.2014,2014:doi:10.1155/2014/593956.
APA:
Li, Rong,Chung, Arthur C. K.,Yu, Xueqing&Lan, Hui Y..(2014).MicroRNAs in Diabetic Kidney Disease.INTERNATIONAL JOURNAL OF ENDOCRINOLOGY,2014,
MLA:
Li, Rong,et al."MicroRNAs in Diabetic Kidney Disease".INTERNATIONAL JOURNAL OF ENDOCRINOLOGY 2014.(2014)