Quantitative structure-cytotoxicity relationships (QSCR) for semi-synthetic Taxoteres against cancer cell lines

被引:0
|
作者
Sivakumar, Ponnurengam Malliappan [1 ]
Vignesh, Naga [1 ]
Senthilkumaran, M. [2 ]
Doble, Mukesh [1 ]
机构
[1] Indian Inst Technol, Dept Biotechnol, Madras 600036, Tamil Nadu, India
[2] Muthayammal Engn Coll, Dept Comp Sci & Engn, Rasipuram 637408, Tamil Nadu, India
关键词
Taxoteres; QSCR; genetic function approximation; adenocarcinoma; p-glycoprotein; ATOMIC PHYSICOCHEMICAL PARAMETERS; BIOLOGICAL EVALUATION; MULTIDRUG-RESISTANCE; P-GLYCOPROTEIN; TAXOL; TRANSPORTERS; DESCRIPTORS; QSAR; MICROTUBULES; MECHANISMS;
D O I
10.1080/08927022.2011.583647
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Cytotoxic activity of 47 semi-synthetic Taxoteres against four different cancer cell lines, such as ovarian cancer (A121), human colon adenocarcinoma (HT29), human breast cancer (MCF7) and drug-resistant human breast cancer (MCF7R), was used to develop a quantitative structure-cytotoxicity relationship (QSCR). The data were divided into training (38) and test sets (9), in which the former was used to develop the QSCR and the later was used for the prediction of three of the cell lines namely A121, HT29 and MCF7. In the case of MCF7R, the training set contained 36 compounds and the test set contained nine compounds. The statistical measures such as squared correlation coefficient (r(2) = 0.73-0.81), adjusted squared correlation coefficient (r(2) adj = 0.72-0.80), cross-correlation coefficient (q(2) = 0.62-0.75) and F-ratio (17.49-27.49) were found to be satisfactory. Other statistical diagnoses such as n/p ratio, fraction of the variance in terms of r(2) and quality factor (Q) were also satisfactory. Thermodynamic, lipophilic/hydrophilic, spatial (Jurs descriptors) and topological (Kier and Hall connectivity indices) descriptors contributed to the activity. Functional groups required at R(1)-R(3) positions for enhanced activity are discussed. The developed QSCR models can be used in the design and development of newer semi-synthetic Taxotere derivatives for the cancer therapy.
引用
收藏
页码:1122 / 1130
页数:9
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