Abstract

BackgroundDuring the last years, several approaches were applied on biomedical data to detect disease specific proteins and genes in order to better target drugs. It was shown that statistical and machine learning based methods use mainly clinical data and improve later their results by adding omics data. This work proposes a new method to discriminate the response of Acute Myeloid Leukemia (AML) patients to treatment. The proposed approach uses proteomics data and prior regulatory knowledge in the form of networks to predict cancer treatment outcomes by finding out the different Boolean networks specific to each type of response to drugs. To show its effectiveness we evaluate our method on a dataset from the DREAM 9 challenge.ResultsThe results are encouraging and demonstrate the benefit of our approach to distinguish patient groups with different response to treatment. In particular each treatment response group is characterized by a predictive model in the form of a signaling Boolean network. This model describes regulatory mechanisms which are specific to each response group. The proteins in this model were selected from the complete dataset by imposing optimization constraints that maximize the difference in the logical response of the Boolean network associated to each group of patients given the omic dataset. This mechanistic and predictive model also allow us to classify new patients data into the two different patient response groups.ConclusionsWe propose a new method to detect the most relevant proteins for understanding different patient responses upon treatments in order to better target drugs using a Prior Knowledge Network and proteomics data. The results are interesting and show the effectiveness of our method.

Highlights

  • During the last years, several approaches were applied on biomedical data to detect disease specific proteins and genes in order to better target drugs

  • In their work they agree with previous studies on the low discriminant power of proteomic data: only two discriminant features came from proteomic data (PIK3CA and GSK3) and the rest were taken from the bio-clinical data

  • We have introduced in [23] the caspo method, which learns Boolean networks (BNs) from phosphoproteomic multiple perturbation data by using Logic Programming

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Summary

Introduction

Several approaches were applied on biomedical data to detect disease specific proteins and genes in order to better target drugs. One quarter of Acute Myeloid Leukemia (AML) diagnosed patients survive beyond 5 years It is worth exploring how mathematical modeling may contribute on a shift towards a more personalized follow up treatment for AML diagnosed patients. In [5] the authors proposed a biomarker detection method for the Dream 9 challenge data, which combines a machine learning framework with prior knowledge concerning the evolutionary conservation of the selected biomarkers. In their work they agree with previous studies on the low discriminant power of proteomic data: only two discriminant features came from proteomic data (PIK3CA and GSK3) and the rest were taken from the bio-clinical data. In this work we aim to understand the impact of using a mathematical model built over a signaling network, automatically retrieved from the KEGG database, associating the measured proteins on the prediction of CR-PR classes of patients’ response

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