DocumentCode
2189902
Title
Dual-Targeted Drug Design of HER2 and HSP90 by CoMFA Model and Pharmacophore Analysis
Author
Huang, Hung-Jin ; Bau, Da-Tian ; Tsai, Ming-Hsui ; Hsu, Yuan-Man ; Ho, Tin-Yun ; Chen, Chien-Yu ; Chang, Yea- Huey ; Tsai, Fuu-Jen ; Tsai, Chang-Hai ; Chen, Calvin Yu-Chian
Author_Institution
Dept. of Biol. Sci. & Technol., China Med. Univ., Taichung, Taiwan
fYear
2009
fDate
17-19 Oct. 2009
Firstpage
1
Lastpage
5
Abstract
Heat shock protein 90 (HSP90) and human epidermal growth factor receptor 2 protein (HER2) are involved in several signal pathways for cancer cell proliferation. We focused on these two hallmarkers to design the dual-targeted inhibitors for cancer therapy. The comparative molecular field analysis (CoMFA) and pharmacophore analysis were employed for generating the predictive models. According the leave-one out (LOO) cross-validation, the CoMFA models obtained the significant r2 values of 0.978 and 0.974 for HSP90 and HER2, respectively. The contour maps of both targets indicated that there were amount of similar bulky favors area. Besides, the cost difference of pharmacophore models was 48.539 for 70% correlation with the experiment. The queries at 3-N and 6-N position of purine-based compound had the similar distributions. This study provided important information for design the HER2 and HSP90 dual-targeted inhibitors.
Keywords
bioinformatics; cancer; drugs; inhibitors; molecular biophysics; proteins; 3D QSAR; HER2; HSP90; cancer cell proliferation; cancer therapy; comparative molecular field analysis; dual-targeted drug design; dual-targeted inhibitors; heat shock protein 90; human epidermal growth factor receptor 2 protein; leave-one out cross-validation; pharmacophore analysis; Cancer; Costs; Drugs; Electric shock; Epidermis; Humans; Inhibitors; Medical treatment; Predictive models; Proteins;
fLanguage
English
Publisher
ieee
Conference_Titel
Biomedical Engineering and Informatics, 2009. BMEI '09. 2nd International Conference on
Conference_Location
Tianjin
Print_ISBN
978-1-4244-4132-7
Electronic_ISBN
978-1-4244-4134-1
Type
conf
DOI
10.1109/BMEI.2009.5305352
Filename
5305352
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