Oncotarget

Research Papers:

Systematic analysis of the expression profile of non-coding RNAs involved in ischemia/reperfusion-induced acute kidney injury in mice using RNA sequencing

Jun Zhou _, Hongtao Chen and Youling Fan

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Oncotarget. 2017; 8:100196-100215. https://doi.org/10.18632/oncotarget.22130

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Abstract

Jun Zhou1, Hongtao Chen2 and Youling Fan3

1Department of Anesthesiology, The First People’s Hospital of Foshan, Foshan, Guangdong Province 528000, China

2Department of Anesthesiology, Eighth People’s Hospital of Guangzhou, Guangzhou, Guangdong Province 510060, China

3Department of Anesthesiology, Panyu Central Hospital, Guangzhou, Guangdong Province 511400, China

Correspondence to:

Jun Zhou, email: [email protected]

Keywords: ischemia/reperfusion; acute kidney injury; non-coding RNAs; sequencing data analysis; expression profiles difference

Received: July 13, 2017    Accepted: August 27, 2017    Published: October 26, 2017

ABSTRACT

Acute kidney injury (AKI) is a common and serious disease characterized by a rapid decline in renal function and has an unacceptably high mortality rate with no effective treatment beyond supportive care. AKI can be induced by many factors such as ischemia/reperfusion (IR), sepsis, and drug-induced nephrotoxicity. However, the molecular mechanisms of AKI are poorly understood. A non-coding RNA (ncRNA) is a RNA molecule that is not translated into a protein. NcRNAs play multiple roles in cellular processes, and mutations or imbalances of these molecules within the body can cause a variety of diseases. Although growing evidence has supported the key role of ncRNAs in AKI, the specific mechanism remains largely unknown. In this study, the second-generation gene sequencing was performed to investigate the expression patterns of ncRNAs, including microRNA (miRNA), long non-coding RNAs, and circular RNAs, in the kidneys of mice subjected to IR-induced AKI. This information will contribute to future research of the mechanism of ncRNAs in the pathogenesis of AKI and facilitate the identification of novel therapeutic targets of ncRNAs.


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