Identification of topological features in renal tumor microenvironment associated with patient survival

被引:64
作者
Cheng, Jun [1 ]
Mo, Xiaokui [2 ]
Wang, Xusheng [3 ]
Parwani, Anil [4 ]
Feng, Qianjin [1 ]
Huang, Kun [3 ,5 ,6 ]
机构
[1] Southern Med Univ, Sch Biomed Engn, Guangdong Prov Key Lab Med Image Proc, Guangzhou 510515, Guangdong, Peoples R China
[2] Ohio State Univ, Wexner Med Ctr, Ctr Biostat, Columbus, OH 43210 USA
[3] Ohio State Univ, Dept Elect & Comp Engn, Columbus, OH 43210 USA
[4] Ohio State Univ, Dept Pathol, Columbus, OH 43210 USA
[5] Ohio State Univ, Dept Biomed Informat, Columbus, OH 43210 USA
[6] Indiana Univ Sch Med, Dept Med, Indianapolis, IN 46202 USA
关键词
HISTOPATHOLOGICAL IMAGE-ANALYSIS; CELL CARCINOMA; BREAST-CANCER; HISTOLOGIC SUBTYPES; PROGNOSTIC UTILITY; ROC CURVES; CLASSIFICATION; ACCURACY;
D O I
10.1093/bioinformatics/btx723
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: As a highly heterogeneous disease, the progression of tumor is not only achieved by unlimited growth of the tumor cells, but also supported, stimulated, and nurtured by the microenvironment around it. However, traditional qualitative and/or semi-quantitative parameters obtained by pathologist's visual examination have very limited capability to capture this interaction between tumor and its microenvironment. With the advent of digital pathology, computerized image analysis may provide a better tumor characterization and give new insights into this problem. Results: We propose a novel bioimage informatics pipeline for automatically characterizing the topological organization of different cell patterns in the tumor microenvironment. We apply this pipeline to the only publicly available large histopathology image dataset for a cohort of 190 patients with papillary renal cell carcinoma obtained from The Cancer Genome Atlas project. Experimental results show that the proposed topological features can successfully stratify early- and middle-stage patients with distinct survival, and show superior performance to traditional clinical features and cellular morphological and intensity features. The proposed features not only provide new insights into the topological organizations of cancers, but also can be integrated with genomic data in future studies to develop new integrative biomarkers.
引用
收藏
页码:1024 / 1030
页数:7
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