Statins Inhibit Toll-Like Receptor 4–Mediated Growth of Human Esophageal Adenocarcinoma Cells

Author(s):  
Anna K. Gergen ◽  
Patrick D. Kohtz ◽  
Alison L. Halpern ◽  
Allana M. White ◽  
Xianzhong Meng ◽  
...  
Helicobacter ◽  
2021 ◽  
Author(s):  
Carolina Hernández ◽  
Karen Toledo‐Stuardo ◽  
Paulina García‐González ◽  
Macarena Garrido‐Tapia ◽  
Karina Kramm ◽  
...  

2011 ◽  
Vol 140 (5) ◽  
pp. S-220
Author(s):  
Romy E. Verbeek ◽  
Peter D. Siersema ◽  
Fiebo J. ten Kate ◽  
Kees Fluiter ◽  
Frank P. Vleggaar ◽  
...  

2019 ◽  
Vol 107 (1) ◽  
pp. 233-241 ◽  
Author(s):  
Patrick D. Kohtz ◽  
Alison L. Halpern ◽  
Mohamed A. Eldeiry ◽  
Kweku Hazel ◽  
Shana Kalatardi ◽  
...  

2012 ◽  
Vol 142 (5) ◽  
pp. S-165-S-166
Author(s):  
Romy E. Verbeek ◽  
Peter D. Siersema ◽  
Pauline Bus ◽  
Fiebo J. ten Kate ◽  
Kees Fluiter ◽  
...  

2007 ◽  
Vol 6 (1) ◽  
pp. 142-143
Author(s):  
A RIAD ◽  
S BIEN ◽  
M GRATZ ◽  
S BERESWILL ◽  
H SCHULTHEISS ◽  
...  

VASA ◽  
2014 ◽  
Vol 43 (1) ◽  
pp. 39-46 ◽  
Author(s):  
Tao Shang ◽  
Feng Ran ◽  
Qian Qiao ◽  
Zhao Liu ◽  
Chang-Jian Liu

Background: The purpose of this study was to determine whether myeloid differentiation factor88-dependent Toll-Like Receptor-4 (TLR-4) signaling contributed to the inhibition of abdominal aortic aneurysm (AAA) by Tanshinone IIA (Tan IIA). Materials and methods: Male Sprague-Dawley rats (n = 12 / group) were randomly distributed into three groups: Tan IIA, control, and sham. The rats from Tan IIA and control groups under-went intra-aortic elastase perfusion to induce AAAs, and those in the sham group were perfused with saline. Only the Tan IIA group received Tan IIA (2 mg / rat / d). Aortic tissue samples were harvested at 24 d after perfusion and evaluated using reverse transcriptase-polymerase chain reaction, Western blot, immunohistochemistry and immunofluorescence. Results: The over-expression of Toll-Like Receptor-4 (TLR-4), Myeloid Differentiation factor 88 (MyD88), Phosphorylated Nuclear Factor κB (pNF-κB) and Phosphorylated IκBα (pIκBα) induced by elastase perfusion were significantly decreased by Tan IIA treatment. Conclusions: Tan IIA attenuates elastase-induced AAA in rats possibly via the inhibition of MyD88-dependent TLR-4 signaling, which may be one potential explanation of why Tan IIA inhibits AAA development through multiple effects.


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