Cysteine‐rich protein 61, a specific ultra‐early biomarker in kidney ischemia/reperfusion injury
CYR61
DOI:
10.1111/nep.13513
Publication Date:
2018-10-17T08:32:44Z
AUTHORS (7)
ABSTRACT
ABSTRACT Aim Studies have shown that cysteine‐rich protein 61 (Cyr61) increased in the post‐ischemic human kidney tissue. However, it is still unknown whether Cyr61 can be used as a biomarker ischemia/reperfusion (I/R) injury. Methods Microarray data were collected from GSE58438 and GSE52004. The rat I/R model was established to evaluate messenger RNA expression of Cyr61, localization by immunohistochemical immunofluorescence staining, changes serum creatinine (Scr) at same time. Results Bioinformatics result showed significantly 3 h after kidney, involved angiogene, positive regulation locomotion single organism cell adhesion. results mainly expressed renal tubular epithelial cells with injury up‐regulated 1 h, peaked 4–8 began decay 12 h. area under curve receiver operating characteristics tissue urine 90.2% 86.1%, which all better than Scr 67.1% ( P < 0.05). Conclusion We made preliminary investigation relationship between AKI, identifies may replace an ultra‐early new AKI.
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