Integrating multi-type aberrations from DNA and RNA through dynamic mapping gene space for subtype-specific breast cancer driver discovery

Author:

Xi Jianing1ORCID,Deng Zhen2,Liu Yang1ORCID,Wang Qian1,Shi Wen1

Affiliation:

1. School of Biomedical Engineering, Guangzhou Medical University, Guangzhou, China

2. School of Basic Medical Sciences, Guangzhou Medical University, Guangzhou, China

Abstract

Driver event discovery is a crucial demand for breast cancer diagnosis and therapy. In particular, discovering subtype-specificity of drivers can prompt the personalized biomarker discovery and precision treatment of cancer patients. Still, most of the existing computational driver discovery studies mainly exploit the information from DNA aberrations and gene interactions. Notably, cancer driver events would occur due to not only DNA aberrations but also RNA alternations, but integrating multi-type aberrations from both DNA and RNA is still a challenging task for breast cancer drivers. On the one hand, the data formats of different aberration types also differ from each other, known as data format incompatibility. On the other hand, different types of aberrations demonstrate distinct patterns across samples, known as aberration type heterogeneity. To promote the integrated analysis of subtype-specific breast cancer drivers, we design a “splicing-and-fusing” framework to address the issues of data format incompatibility and aberration type heterogeneity simultaneously. To overcome the data format incompatibility, the “splicing-step” employs a knowledge graph structure to connect multi-type aberrations from the DNA and RNA data into a unified formation. To tackle the aberration type heterogeneity, the “fusing-step” adopts a dynamic mapping gene space integration approach to represent the multi-type information by vectorized profiles. The experiments also demonstrate the advantages of our approach in both the integration of multi-type aberrations from DNA and RNA and the discovery of subtype-specific breast cancer drivers. In summary, our “splicing-and-fusing” framework with knowledge graph connection and dynamic mapping gene space fusion of multi-type aberrations data from DNA and RNA can successfully discover potential breast cancer drivers with subtype-specificity indication.

Funder

National Natural Science Foundation of China

Special Foundation in Department of Higher Education of Guangdong

Publisher

PeerJ

Subject

General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

Reference56 articles.

1. Toward understanding and exploiting tumor heterogeneity;Alizadeh;Nature Medicine,2015

2. Detecting recurrent gene mutation in interaction network context using multi-scale graph diffusion;Babaei;BMC Bioinformatics,2013

3. Comprehensive characterization of cancer driver genes and mutations;Bailey;Cell,2018

4. Translating embeddings for modeling multi-relational data;Bordes,2013

5. Genomic basis for rna alterations in cancer;Calabrese;Nature,2020

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