REAL

A network-based target overlap score for characterizing drug combinations: High correlation with cancer clinical trial results

Ligeti, Balázs and Pénzváltó, Zsófia and Vera, Roberto and Győrffy, Balázs and Pongor, Sándor (2015) A network-based target overlap score for characterizing drug combinations: High correlation with cancer clinical trial results. PLOS ONE, 10 (6). pp. 1-18. ISSN 1932-6203

[img]
Preview
Text
gyorffy_plos_one_2015_u.pdf

Download (1MB) | Preview

Abstract

Drug combinations are highly efficient in systemic treatment of complex multigene diseases such as cancer, diabetes, arthritis and hypertension. Most currently used combinations were found in empirical ways, which limits the speed of discovery for new and more effective combinations. Therefore, there is a substantial need for efficient and fast computational methods. Here, we present a principle that is based on the assumption that perturbations generated by multiple pharmaceutical agents propagate through an interaction network and can cause unexpected amplification at targets not immediately affected by the original drugs. In order to capture this phenomenon, we introduce a novel Target Overlap Score (TOS) that is defined for two pharmaceutical agents as the number of jointly perturbed targets divided by the number of all targets potentially affected by the two agents. We show that this measure is correlated with the known effects of beneficial and deleterious drug combinations taken from the DCDB, TTD and Drugs.com databases. We demonstrate the utility of TOS by correlating the score to the outcome of recent clinical trials evaluating trastuzumab, an effective anticancer agent utilized in combination with anthracycline- and taxane-based systemic chemotherapy in HER2-receptor (erb-b2 receptor tyrosine kinase 2) positive breast cancer. © 2015 Ligeti et al.

Item Type: Article
Uncontrolled Keywords: CHEMOTHERAPY; ARTICLE; SIGNAL TRANSDUCTION; human; CYCLOPHOSPHAMIDE; drug response; statistical analysis; outcome assessment; scoring system; drug efficacy; clinical practice; area under the curve; anthracycline; protein protein interaction; breast cancer; cancer survival; cancer combination chemotherapy; mitogen activated protein kinase 1; trastuzumab; taxane derivative; carboplatin; Sample Size; factual database; Raf protein; epidermal growth factor receptor 2; mitogen activated protein kinase kinase 1; hypothesis; clinical trial (topic); progression free survival; oxaliplatin; classifier; Toscana virus; Target Overlap Score; systemic chemotherapy; statistical bias; network interaction hypothesis; ixabepilone;
Subjects: R Medicine / orvostudomány > R1 Medicine (General) / orvostudomány általában > R850-854 Experimental medicine / kisérleti orvostudomány
SWORD Depositor: MTMT SWORD
Depositing User: MTMT SWORD
Date Deposited: 17 Dec 2018 13:52
Last Modified: 17 Dec 2018 13:52
URI: http://real.mtak.hu/id/eprint/88641

Actions (login required)

Edit Item Edit Item