Integrative Analysis of Pathological Images and Multi-Dimensional Genomic Data for Early-Stage Cancer Prognosis

被引:63
|
作者
Shao, Wei [1 ]
Huang, Kun [2 ]
Han, Zhi [2 ]
Cheng, Jun [3 ]
Cheng, Liang [2 ]
Wang, Tongxin [4 ]
Sun, Liang [1 ]
Lu, Zixiao [2 ]
Zhang, Jie [2 ]
Zhang, Daoqiang [1 ]
机构
[1] Nanjing Univ Aeronaut & Astronaut, MIIT Key Lab Pattern Anal & Machine Intelligence, Coll Comp Sci & Technol, Nanjing 211106, Peoples R China
[2] Indiana Univ, Sch Med, Indianapolis, IN 46202 USA
[3] Shenzhen Univ, Sch Biomed Engn, Shenzhen 518073, Peoples R China
[4] Indiana Univ, Dept Comp Sci, Bloomington, IN 47405 USA
基金
中国国家自然科学基金;
关键词
Feature extraction; Cancer; Genomics; Bioinformatics; Prognostics and health management; DNA; Histopathological images; multi-modal genomic data; survival analysis; early-stage cancer; ordinal multi-model feature selection; LUNG-CANCER; CELL; CYTOKINE; POLYMORPHISMS; MECHANISMS; EXPRESSION; APOPTOSIS; MODULES; BREAST;
D O I
10.1109/TMI.2019.2920608
中图分类号
TP39 [计算机的应用];
学科分类号
081203 ; 0835 ;
摘要
The integrative analysis of histopathological images and genomic data has received increasing attention for studying the complex mechanisms of driving cancers. However, most image-genomic studies have been restricted to combining histopathological images with the single modality of genomic data (e.g., mRNA transcription or genetic mutation), and thus neglect the fact that the molecular architecture of cancer is manifested at multiple levels, including genetic, epigenetic, transcriptional, and post-transcriptional events. To address this issue, we propose a novel ordinal multi-modal feature selection (OMMFS) framework that can simultaneously identify important features from both pathological images and multi-modal genomic data (i.e., mRNA transcription, copy number variation, and DNA methylation data) for the prognosis of cancer patients. Our model is based on a generalized sparse canonical correlation analysis framework, by which we also take advantage of the ordinal survival information among different patients for survival outcome prediction. We evaluate our method on three early-stage cancer datasets derived from The Cancer Genome Atlas (TCGA) project, and the experimental results demonstrated that both the selected image and multi-modal genomic markers are strongly correlated with survival enabling effective stratification of patients with distinct survival than the comparing methods, which is often difficult for early-stage cancer patients.
引用
收藏
页码:99 / 110
页数:12
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