Cervical changes in estrogen receptor alpha, oxytocin receptor, LH receptor, and cyclooxygenase-2 depending on the histologic compartment, longitudinal axis, and day of the ovine estrous cycle

2014 ◽  
Vol 81 (6) ◽  
pp. 813-824 ◽  
Author(s):  
M. Rodríguez-Piñón ◽  
R. Gonzalez ◽  
C. Tasende ◽  
A. Bielli ◽  
P. Genovese ◽  
...  
2015 ◽  
Vol 15 (3) ◽  
pp. 274-280 ◽  
Author(s):  
Enade Perdana Istyastono ◽  
Florentinus Dika Octa Riswanto ◽  
Sri Hartati Yuliani

A cyclooxygenase-2 (COX-2) inhibitor celecoxib has been previously reported to have cytotoxic activities towards gastric, prostate, ovarian, colon and breast cancer cell lines. This article reports that the cytotoxic activities of celecoxib could be resulted from its activity as a potent ligand for estrogen receptor alpha (ERα). Aided by molecular docking simulations, an in silico test to examine whether celecoxib is a ligand for estrogen receptor alpha (ERα) was performed followed by in vitro test employing cytotoxic assay using 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide (MTT) method. The compound was extracted from Celebrex®. Measured by using UV spectrophotometric method at 255.5 nm, it was identified that the content of celecoxib was 102.15 mg/271.48 mg capsule content. The in silico test indicated that celecoxib is a potent ligand for ERα. This finding was confirmed experimentally by an in vitro test that celecoxib has a comparable activity as an ERα ligand to tamoxifen, a drug of choice for breast cancer treatment.


Endocrine ◽  
2007 ◽  
Vol 31 (2) ◽  
pp. 154-160 ◽  
Author(s):  
Hossein Pournajafi-Nazarloo ◽  
Eros Papademeteriou ◽  
Leila Partoo ◽  
Habibollah Saadat ◽  
Bruce S. Cushing

2009 ◽  
Vol 19 (2) ◽  
pp. 173-178
Author(s):  
Sukanya Manee-in ◽  
Sayamon Srisuwatanasagul ◽  
Chainarong Lohachit ◽  
Junpen Suwimonteerabutr ◽  
Sudson Sirivaidyapong

2007 ◽  
Vol 77 (Suppl_1) ◽  
pp. 106-106
Author(s):  
Luciano Mendoza-Garces ◽  
Paola Artega-Lopez ◽  
Roberto Domínguez ◽  
Marco Cerbon ◽  
Isabel Arrieta-Cruz ◽  
...  

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