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Damage Intensity of Carvacrol on Prostatic Cancer Cells Linedu145 and Molecular Dynamic Simulation of It Effect on Apoptotic Factors



Chaleshtori JS1 ; Soreshjani EH2 ; Reisi F3 ; Tabatabaiefar MA4 ; Asadisamani M5 ; Navid Z6 ; Bahmani M7
Authors
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Authors Affiliations
  1. 1. Cellular and Molecular Research Center, Shahrekord University of Medical Sciences, Shahrekord, Iran
  2. 2. Young Researchers and Elites Club, Islamic Azad University, Shahrekord Branch, Shahrekord, Iran
  3. 3. Department of Biology, Faculty of Basic Sciences, Shahrekord Branch, Islamic Azad University, Shahrekord, Iran
  4. 4. Department of Genetics and Molecular Biology, School of Medicine, IsfahanUniversity of Medical Sciences, Isfahan, Iran
  5. 5. Medical Plants Research Center, Shahrekord University of Medical Sciences, Shahrekord, Iran
  6. 6. Computer Engineer, Iran Technical & Vocational Training Organization, Shahrekord, Iran
  7. 7. Razi Herbal Medicines Research Center, Lorestan University of Medical Sciences, Khorramabad, Iran

Source: International Journal of PharmTech Research Published:2016

Abstract

Prostatic cancer is one of the most dangerous diseases in men worldwide. The apoptotic factors such as BID, BIM and APAF1 have a main role in inducing apoptotic pathways. On the other hand, some compounds can active this apoptotic factors. In this study, this notion was investigated by the use of the comet assay technique and molecular dynamics simulations. In the comet assay technique, different concentrations including 130, 230, and 360 μM of Carvacrol were selected according to IC50 using MTT assay on the cell line DU145. Then, alkaline electrophoresis was performed and 100 comet pictures were analyzed using CASP software. Data were analyzed by SPSS statistical software and also using molecular dynamics simulations, wherein protein and Carvacrol were studied, thus avoiding the necessity for quantum mechanical calculations. Molecular dynamics simulations were carried out using with Carvacrol closed in a fully hydrated simulation box with a protein (Bak, Bax, Bim, Apaf1, Bid and P38). The IC50 for Carvacrol was determined at 360μM by MTT test. Rate of tail to head in alkaline electrophoresis at 130, 230, and 360 μM of Carvacrol concentrations were 13. 8±0. 3, 40. 6±0. 3, and 47. 6±0. 5 percent, respectively. Statistical analysis of the molecular dynamics and calculated potential energy, radius of gyration (Rg), temperature, root mean square fluctuation (RMSF) and root mean square deviation (RMSD) indicated that Carvacrol affected protein which stimulated the apoptosis cascade. Therefore, both experimental and theoretical results demonstrate carvacrol directly affects factors initiating apoptosis. © 2016, Sphinx Knowledge House. All rights reserved.
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