Beta-Thalassemia is an inherited hematologic disorder caused by various mutations of the beta-globin gene, thus resulting in a significant decrease in adult hemoglobin (HbA) production. An increase in fetal hemoglobin (HbF) levels by drug molecules is considered of great potential in β-thalassemia treatment and is expected to counterbalance the impaired production of HbA. In this work, based on a set of 129 experimentally tested biological inhibitors, we developed and validated a computational model for the prediction of K562 functional inhibition, possibly associated with HbF induction. To facilitate future advancements in the field, we incorporated our model into Enalos Cloud Platform, which enabled online access to our computational scheme (http://enalos.insilicotox.com/K562) through a user-friendly interface. This web service is offered to the wider community to promote insilico drug discovery through fast and reliable predictions.

Consensus Predictive Model for Human K562 Cell Growth Inhibition through Enalos Cloud Platform

Gambari, Roberto
Penultimo
;
2018

Abstract

Beta-Thalassemia is an inherited hematologic disorder caused by various mutations of the beta-globin gene, thus resulting in a significant decrease in adult hemoglobin (HbA) production. An increase in fetal hemoglobin (HbF) levels by drug molecules is considered of great potential in β-thalassemia treatment and is expected to counterbalance the impaired production of HbA. In this work, based on a set of 129 experimentally tested biological inhibitors, we developed and validated a computational model for the prediction of K562 functional inhibition, possibly associated with HbF induction. To facilitate future advancements in the field, we incorporated our model into Enalos Cloud Platform, which enabled online access to our computational scheme (http://enalos.insilicotox.com/K562) through a user-friendly interface. This web service is offered to the wider community to promote insilico drug discovery through fast and reliable predictions.
2018
Afantitis, Antreas; Leonis, Georgios; Gambari, Roberto; Melagraki, Georgia
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11392/2383624
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