Validation of quantitative structure-activity relationship (QSAR) model for photosensitizer activity prediction

Photodynamic therapy is a relatively new treatment method for cancer which utilizes a combination of oxygen, a photosensitizer and light to generate reactive singlet oxygen that eradicates tumors via direct cell-killing, vasculature damage and engagement of the immune system. Most of photosensitizer...

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Main Authors: Frimayanti, N., Yam, M.L., Lee, H.B., Othman, R., Zain, Sharifuddin Md, Rahman, N.A.
Format: Article
Language:English
Published: 2011
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Online Access:http://eprints.um.edu.my/3459/1/22.pdf
http://eprints.um.edu.my/3459/
http://www.ncbi.nlm.nih.gov/pubmed/22272096
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spelling my.um.eprints.34592019-10-25T09:11:16Z http://eprints.um.edu.my/3459/ Validation of quantitative structure-activity relationship (QSAR) model for photosensitizer activity prediction Frimayanti, N. Yam, M.L. Lee, H.B. Othman, R. Zain, Sharifuddin Md Rahman, N.A. R Medicine Photodynamic therapy is a relatively new treatment method for cancer which utilizes a combination of oxygen, a photosensitizer and light to generate reactive singlet oxygen that eradicates tumors via direct cell-killing, vasculature damage and engagement of the immune system. Most of photosensitizers that are in clinical and pre-clinical assessments, or those that are already approved for clinical use, are mainly based on cyclic tetrapyrroles. In an attempt to discover new effective photosensitizers, we report the use of the quantitative structure-activity relationship (QSAR) method to develop a model that could correlate the structural features of cyclic tetrapyrrole-based compounds with their photodynamic therapy (PDT) activity. In this study, a set of 36 porphyrin derivatives was used in the model development where 24 of these compounds were in the training set and the remaining 12 compounds were in the test set. The development of the QSAR model involved the use of the multiple linear regression analysis (MLRA) method. Based on the method, r(2) value, r(2) (CV) value and r(2) prediction value of 0.87, 0.71 and 0.70 were obtained. The QSAR model was also employed to predict the experimental compounds in an external test set. This external test set comprises 20 porphyrin-based compounds with experimental IC(50) values ranging from 0.39 μM to 7.04 μM. Thus the model showed good correlative and predictive ability, with a predictive correlation coefficient (r(2) prediction for external test set) of 0.52. The developed QSAR model was used to discover some compounds as new lead photosensitizers from this external test set. 2011 Article PeerReviewed application/pdf en http://eprints.um.edu.my/3459/1/22.pdf Frimayanti, N. and Yam, M.L. and Lee, H.B. and Othman, R. and Zain, Sharifuddin Md and Rahman, N.A. (2011) Validation of quantitative structure-activity relationship (QSAR) model for photosensitizer activity prediction. International Journal of Molecular Sciences, 12 (12). http://www.ncbi.nlm.nih.gov/pubmed/22272096
institution Universiti Malaya
building UM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaya
content_source UM Research Repository
url_provider http://eprints.um.edu.my/
language English
topic R Medicine
spellingShingle R Medicine
Frimayanti, N.
Yam, M.L.
Lee, H.B.
Othman, R.
Zain, Sharifuddin Md
Rahman, N.A.
Validation of quantitative structure-activity relationship (QSAR) model for photosensitizer activity prediction
description Photodynamic therapy is a relatively new treatment method for cancer which utilizes a combination of oxygen, a photosensitizer and light to generate reactive singlet oxygen that eradicates tumors via direct cell-killing, vasculature damage and engagement of the immune system. Most of photosensitizers that are in clinical and pre-clinical assessments, or those that are already approved for clinical use, are mainly based on cyclic tetrapyrroles. In an attempt to discover new effective photosensitizers, we report the use of the quantitative structure-activity relationship (QSAR) method to develop a model that could correlate the structural features of cyclic tetrapyrrole-based compounds with their photodynamic therapy (PDT) activity. In this study, a set of 36 porphyrin derivatives was used in the model development where 24 of these compounds were in the training set and the remaining 12 compounds were in the test set. The development of the QSAR model involved the use of the multiple linear regression analysis (MLRA) method. Based on the method, r(2) value, r(2) (CV) value and r(2) prediction value of 0.87, 0.71 and 0.70 were obtained. The QSAR model was also employed to predict the experimental compounds in an external test set. This external test set comprises 20 porphyrin-based compounds with experimental IC(50) values ranging from 0.39 μM to 7.04 μM. Thus the model showed good correlative and predictive ability, with a predictive correlation coefficient (r(2) prediction for external test set) of 0.52. The developed QSAR model was used to discover some compounds as new lead photosensitizers from this external test set.
format Article
author Frimayanti, N.
Yam, M.L.
Lee, H.B.
Othman, R.
Zain, Sharifuddin Md
Rahman, N.A.
author_facet Frimayanti, N.
Yam, M.L.
Lee, H.B.
Othman, R.
Zain, Sharifuddin Md
Rahman, N.A.
author_sort Frimayanti, N.
title Validation of quantitative structure-activity relationship (QSAR) model for photosensitizer activity prediction
title_short Validation of quantitative structure-activity relationship (QSAR) model for photosensitizer activity prediction
title_full Validation of quantitative structure-activity relationship (QSAR) model for photosensitizer activity prediction
title_fullStr Validation of quantitative structure-activity relationship (QSAR) model for photosensitizer activity prediction
title_full_unstemmed Validation of quantitative structure-activity relationship (QSAR) model for photosensitizer activity prediction
title_sort validation of quantitative structure-activity relationship (qsar) model for photosensitizer activity prediction
publishDate 2011
url http://eprints.um.edu.my/3459/1/22.pdf
http://eprints.um.edu.my/3459/
http://www.ncbi.nlm.nih.gov/pubmed/22272096
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