scholarly journals Erratum to: Over-expression of Toll-like receptor 2 up-regulates heme oxygenase-1 expression and decreases oxidative injury in dairy goats

2017 ◽  
Vol 8 (1) ◽  
Author(s):  
Shoulong Deng ◽  
Kun Yu ◽  
Wuqi Jiang ◽  
Yan Li ◽  
Sutian Wang ◽  
...  
Keyword(s):  
Heme Oxygenase ◽  
Oxidative Injury ◽  
Heme Oxygenase 1 ◽  
Toll Like Receptor ◽  
Dairy Goats ◽  
Over Expression ◽  
Toll Like Receptor 2

Toll-like receptor 2 contributes to glial cell activation and heme oxygenase-1 expression in traumatic brain injury

2008 ◽  
Vol 431 (2) ◽  
pp. 123-128 ◽  
Author(s):  
Chanhee Park ◽  
Ik-Hyun Cho ◽  
Donghoon Kim ◽  
Eun-Kyeong Jo ◽  
Se-Young Choi ◽  
...  
Keyword(s):  
Traumatic Brain Injury ◽  
Brain Injury ◽  
Glial Cell ◽  
Heme Oxygenase ◽  
Cell Activation ◽  
Heme Oxygenase 1 ◽  
Toll Like Receptor ◽  
Glial Cell Activation ◽  
Toll Like Receptor 2

Heme Oxygenase-1 protects astroglia against manganese-induced oxidative injury by regulating mitochondrial quality control

2018 ◽  
Vol 295 ◽  
pp. 357-368 ◽  
Author(s):  
Roxana Mayra Gorojod ◽  
Agustina Alaimo ◽  
Soledad Porte Alcon ◽  
Jimena Hebe Martinez ◽  
María Eugenia Cortina ◽  
...  
Keyword(s):  
Quality Control ◽  
Heme Oxygenase ◽  
Oxidative Injury ◽  
Heme Oxygenase 1 ◽  
Mitochondrial Quality Control

Glomerular Epithelial Cells-Targeted Heme Oxygenase-1 Over Expression in the Rat: Attenuation of Proteinuria in Secondary But Not Primary Injury

Nephron ◽  
2016 ◽  
Vol 133 (4) ◽  
pp. 270-278 ◽  
Author(s):  
Vassilios Atsaves ◽  
Panagiota Makri ◽  
Maria G. Detsika ◽  
Alexandra Tsirogianni ◽  
Elias A. Lianos
Keyword(s):  
Epithelial Cells ◽  
Heme Oxygenase ◽  
Heme Oxygenase 1 ◽  
Over Expression ◽  
Glomerular Epithelial Cells ◽  
Primary Injury

scholarly journals Antimelanoma activities of chimeric thiazole–androstenone derivatives

2021 ◽  
Vol 8 (8) ◽  
pp. 210395
Author(s):  
Steven A. Chambers ◽  
Mathew Newman ◽  
Melissa M. Frangie ◽  
Alena V. Savenka ◽  
Alexei. G. Basnakian ◽  
...  
Keyword(s):  
Growth Inhibition ◽  
Heme Oxygenase ◽  
Oxidative Injury ◽  
Melanoma Cells ◽  
Tunel Assay ◽  
Heme Oxygenase 1 ◽  
Endonuclease G ◽  
Caspase Activated Dnase ◽  
Potent Growth

The discovery of chimeric anti-melanoma agents is reported. These molecules are potent growth suppressors of melanoma cells in vitro with growth inhibition of 50% (GI 50 ) values as low as 1.32 µM. Compounds were more toxic to melanoma cells in vitro than commonly used anti-melanoma agent dacarbazine as measured by TUNEL assay. They induced both caspase-independent apoptosis evident by colocalization of TUNEL with endonuclease G (EndoG) and caspase-mediated apoptosis measured by colocalization of TUNEL with caspase-activated DNase (CAD). In addition, compounds 3 and 5 strongly induced oxidative injury to melanoma cells as measured by TUNEL colocalization with heme oxygenase-1 (HO1). Dacarbazine induced only caspase-independent apoptosis, which may explain why it is less cytotoxic to melanoma cells than compounds 3 , 4 and 5 .

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