Simultaneous Prediction of four ATP-binding Cassette Transporters’ Substrates Using Multi-label QSAR

Research output: Contribution to journalArticlepeer-review

Abstract

Efflux by the ATP-binding cassette (ABC) transporters affects the pharmacokinetic profile of drugs and it has been implicated in drug-drug interactions as well as its major role in multi-drug resistance in cancer. It is therefore important for the pharmaceutical industry to be able to understand what phenomena rule ABC substrate recognition. Considering a high degree of substrate overlap between various members of ABC transporter family, it is advantageous to employ a multi-label classification approach where predictions made for one transporter can be used for modeling of the other ABC transporters. Here, we present decision tree-based QSAR classification models able to simultaneously predict substrates and non-substrates for BCRP1, P-gp/MDR1 and MRP1 and MRP2, using a dataset of 1493 compounds. To this end, two multi-label classification QSAR modelling approaches were adopted: Binary Relevance (BR) and Classifier Chain (CC). Even though both multi-label models yielded similar predictive performances in terms of overall accuracies (close to 70 %), the CC model overcame the problem of skewed performance towards identifying substrates compared with non-substrates, which is a common problem in the literature. The models were thoroughly validated by using external testing, applicability domain and activity cliffs characterization. In conclusion, a multi-label classification approach is an appropriate alternative for the prediction of ABC efflux.

Original languageEnglish
Pages (from-to)514-528
Number of pages15
JournalMolecular Informatics
Volume35
Issue number10
DOIs
StatePublished - Oct 1 2016
Externally publishedYes

Bibliographical note

© 2016 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

ASJC Scopus Subject Areas

  • Structural Biology
  • Molecular Medicine
  • Drug Discovery
  • Computer Science Applications
  • Organic Chemistry

Keywords

  • BCRP1
  • Breast Cancer Resistance Protein
  • MRP1
  • MRP2
  • Multi-label Classification
  • Multidrug-resistance Associated Protein
  • P-glycoprotein
  • QSAR, Transporter
  • Reproducibility of Results
  • Models, Molecular
  • Substrate Specificity
  • Algorithms
  • ATP-Binding Cassette Transporters/chemistry
  • Protein Binding
  • Ligands
  • Molecular Structure
  • Quantitative Structure-Activity Relationship

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