DRdriver: identifying drug resistance driver genes using individual-specific gene regulatory network

Author:

Huang Yu-e1,Zhou Shunheng1,Liu Haizhou1,Zhou Xu1,Yuan Mengqin1,Hou Fei1,Chen Sina1,Chen Jiahao1,Wang Lihong2,Jiang Wei1ORCID

Affiliation:

1. Department of Biomedical Engineering, Nanjing University of Aeronautics and Astronautics , Nanjing 211106 , China

2. Department of Pathophysiology, School of Medicine, Southeast University , Nanjing 210009 , China

Abstract

AbstractDrug resistance is one of principal limiting factors for cancer treatment. Several mechanisms, especially mutation, have been validated to implicate in drug resistance. In addition, drug resistance is heterogeneous, which makes an urgent need to explore the personalized driver genes of drug resistance. Here, we proposed an approach DRdriver to identify drug resistance driver genes in individual-specific network of resistant patients. First, we identified the differential mutations for each resistant patient. Next, the individual-specific network, which included the genes with differential mutations and their targets, was constructed. Then, the genetic algorithm was utilized to identify the drug resistance driver genes, which regulated the most differentially expressed genes and the least non-differentially expressed genes. In total, we identified 1202 drug resistance driver genes for 8 cancer types and 10 drugs. We also demonstrated that the identified driver genes were mutated more frequently than other genes and tended to be associated with the development of cancer and drug resistance. Based on the mutational signatures of all driver genes and enriched pathways of driver genes in brain lower grade glioma treated by temozolomide, the drug resistance subtypes were identified. Additionally, the subtypes showed great diversity in epithelial–mesenchyme transition, DNA damage repair and tumor mutation burden. In summary, this study developed a method DRdriver for identifying personalized drug resistance driver genes, which provides a framework for unlocking the molecular mechanism and heterogeneity of drug resistance.

Funder

National Natural Science Foundation of China

Publisher

Oxford University Press (OUP)

Subject

Molecular Biology,Information Systems

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