Integrated morphologic analysis for the identification and characterization of disease subtypes

Autor: Lee Cooper, David A. Gutman, Lisa Scarpace, Christina L. Appin, Tahsin Kurc, Jun Kong, Sharath R. Cholleti, Tom Mikkelsen, Jingjing Gao, Ashish Sharma, Daniel J. Brat, Fusheng Wang, Tony Pan, Carlos S. Moreno, Joel H. Saltz
Rok vydání: 2012
Předmět:
biomedical informatics
Cells
Health Informatics
Genomics
Genome-wide association study
Disease
Computational biology
Biology
Research and Applications
Bioinformatics
03 medical and health sciences
image cytometry
high end computing
middleware
0302 clinical medicine
glioma
emory
genomics
Digital pathology
computer-assisted image analysis
cancer
Humans
spatial database
Epigenetics
Copy-number variation
Cluster analysis
data integration
030304 developmental biology
cell morphology
RFID
Regulation of gene expression
0303 health sciences
imaging
bioinformatics
Prognosis
3. Good health
Gene Expression Regulation
Neoplastic

glioblastomabrain tumor
030220 oncology & carcinogenesis
pathology
Identification (biology)
data management
transcription
Glioblastoma
microarray
temporal database
Genome-Wide Association Study
Zdroj: Journal of the American Medical Informatics Association : JAMIA
ISSN: 1527-974X
1067-5027
DOI: 10.1136/amiajnl-2011-000700
Popis: Background and objective: Morphologic variations of disease are often linked to underlying molecular events and patient outcome, suggesting that quantitative morphometric analysis may provide further insight into disease mechanisms. In this paper a methodology for the subclassification of disease is developed using image analysis techniques. Morphologic signatures that represent patient-specific tumor morphology are derived from the analysis of hundreds of millions of cells in digitized whole slide images. Clustering these signatures aggregates tumors into groups with cohesive morphologic characteristics. This methodology is demonstrated with an analysis of glioblastoma, using data from The Cancer Genome Atlas to identify a prognostically significant morphology-driven subclassification, in which clusters are correlated with transcriptional, genetic, and epigenetic events. Materials and methods: Methodology was applied to 162 glioblastomas from The Cancer Genome Atlas to identify morphology-driven clusters and their clinical and molecular correlates. Signatures of patient-specific tumor morphology were generated from analysis of 200 million cells in 462 whole slide images. Morphology-driven clusters were interrogated for associations with patient outcome, response to therapy, molecular classifications, and genetic alterations. An additional layer of deep, genome-wide analysis identified characteristic transcriptional, epigenetic, and copy number variation events. Results and discussion: Analysis of glioblastoma identified three prognostically significant patient clusters (median survival 15.3, 10.7, and 13.0 months, log rank p=1.4e-3). Clustering results were validated in a separate dataset. Clusters were characterized by molecular events in nuclear compartment signaling including developmental and cell cycle checkpoint pathways. This analysis demonstrates the potential of high-throughput morphometrics for the subclassification of disease, establishing an approach that complements genomics.
Databáze: OpenAIRE