MP-05.05: Possible cytoprotective roles of glyoxalase I and heat shock proteins in acute renal cell injury

Urology ◽  
2007 ◽  
Vol 70 (3) ◽  
pp. 63
Author(s):  
P. Pyo ◽  
M. Hoffman ◽  
R. Simon ◽  
H. Tazaki ◽  
M. Choudhury ◽  
...  
2006 ◽  
Vol 2 (3) ◽  
pp. 149-156 ◽  
Author(s):  
Michael Riordan ◽  
Rajasree Sreedharan ◽  
Michael Kashgarian ◽  
Norman J Siegel

2012 ◽  
Vol 2012 ◽  
pp. 1-13 ◽  
Author(s):  
Earl G. Noble ◽  
Garry X. Shen

Heat shock proteins (Hsp) play critical roles in the body’s self-defense under a variety of stresses, including heat shock, oxidative stress, radiation, and wounds, through the regulation of folding and functions of relevant cellular proteins. Exercise increases the levels of Hsp through elevated temperature, hormones, calcium fluxes, reactive oxygen species (ROS), or mechanical deformation of tissues. Isotonic contractions and endurance- type activities tend to increase Hsp60 and Hsp70. Eccentric muscle contractions lead to phosphorylation and translocation of Hsp25/27. Exercise-induced transient increases of Hsp inhibit the generation of inflammatory mediators and vascular inflammation. Metabolic disorders (hyperglycemia and dyslipidemia) are associated with type 1 diabetes (an autoimmune disease), type 2 diabetes (the common type of diabetes usually associated with obesity), and atherosclerotic cardiovascular disease. Metabolic disorders activate HSF/Hsp pathway, which was associated with oxidative stress, increased generation of inflammatory mediators, vascular inflammation, and cell injury. Knock down of heat shock factor-1 (HSF1) reduced the activation of key inflammatory mediators in vascular cells. Accumulating lines of evidence suggest that the activation of HSF/Hsp induced by exercise or metabolic disorders may play a dual role in inflammation. The benefits of exercise on inflammation and metabolism depend on the type, intensity, and duration of physical activity.


1990 ◽  
Vol 3 (3) ◽  
pp. 207-216 ◽  
Author(s):  
Jean E. Rinaldo ◽  
Michael Gorry ◽  
Robert Strieter ◽  
Hans Cowan ◽  
Rasul Abdolrasulnia ◽  
...  

2014 ◽  
Vol 32 (4_suppl) ◽  
pp. 480-480
Author(s):  
Matteo Brunelli ◽  
Francesco Massari ◽  
Chiara Ciccarese ◽  
Stefano Ferrero ◽  
Giacomo Gazzano ◽  
...  

480 Background: Heat shock proteins (HSP) HSP27 and HSP90 are expressed in response to a wide variety of insults, thus allowing the cell to adapt to stress. In cancer cells, both HSP27 and HSP90 may participate to carcinogenesis, suggesting these chaperones as an appealing target for cancer therapeutics. The role of HSP in the development and progression of renal-cell carcinomas (RCCs) remains to be defined. We sought to evaluate a series of clear cell RCCs. Methods: 388 RCCs with clear cell histology available on 10 tissue microarrays were recruited. Each case was represented by 3 neoplastic cores. All these cases were stratified according to the Mayo Clinic SSIGN (Size, Staging, Grading, Necrosis) score into five prognostic groups with increasing worse prognosis (1 to 5). Immunostainings for HSP27 and 90 were performed. A mean score number from the three cores was set per case (percentage x intensity). Results were detailed per number of scorable cases per SSIGN category (1 to 5). Results: 117 and 122 RCCs were respectively available for HSP90 and HSP27 scoring. The remaining samples were lost due to the lack of tissue sections or to the absence of adequate neoplastic cells scorable. HSP90 scored 4,9 in 32 with SSIGN1, 3,5 in 41 SSIGN2, 4,8 in 11 SSIGN3, 4,2 in 22 SSIGN4 and 5 in 3 SSIGN5 patients. HSP27 scored 4,6 in 33 with SSIGN1, 3,1 in 43 SSIGN2, 2,6 in 11 SSIGN3, 3,6 in 24 SSIGN4 and 2,7 in 3 SSIGN5 patients. A significant trend of increasing value for HSP90 has been observed when comparing cases tabled SSIGN1-2 versus SSIGN3-5 (4,2 to 4,6 mean values) (p=0.05); a minor stratification has been observed for HSP27 (3,8 to 3,9) (p=0.08). Conclusions: In conclusion, HSP90 and HSP27 are variable immunoexpressed in a subset of clear cell RCCs, with a trend to higher prognostic SSIGN score. At light of new emerging targeted-therapies in kidney cancer, we report an increasing suitability of these patients to therapies that target the pathways of heat shock protein molecules. Additional learning of the HSP role in clear cell RCCs carcinogenesis is required to guide future therapeutic developments.


1999 ◽  
pp. 145
Author(s):  
Jan Roigas ◽  
Erik S. Wallen ◽  
Stefan A. Loening ◽  
Pope L. Moseley

1999 ◽  
Vol 22 (3) ◽  
pp. 236-239 ◽  
Author(s):  
A. Bex ◽  
C. Geis ◽  
K. Metz ◽  
S. Kasimir-Bauer ◽  
M.E. Scheulen ◽  
...  

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