DocumentCode :
84202
Title :
Invariant Delineation of Nuclear Architecture in Glioblastoma Multiforme for Clinical and Molecular Association
Author :
Hang Chang ; Ju Han ; Borowsky, A. ; Loss, L. ; Gray, J.W. ; Spellman, P.T. ; Parvin, Bahram
Author_Institution :
Life Sci. Div., Lawrence Berkeley Nat. Lab., Berkeley, CA, USA
Volume :
32
Issue :
4
fYear :
2013
fDate :
Apr-13
Firstpage :
670
Lastpage :
682
Abstract :
Automated analysis of whole mount tissue sections can provide insights into tumor subtypes and the underlying molecular basis of neoplasm. However, since tumor sections are collected from different laboratories, inherent technical and biological variations impede analysis for very large datasets such as The Cancer Genome Atlas (TCGA). Our objective is to characterize tumor histopathology, through the delineation of the nuclear regions, from hematoxylin and eosin (H&E) stained tissue sections. Such a representation can then be mined for intrinsic subtypes across a large dataset for prediction and molecular association. Furthermore, nuclear segmentation is formulated within a multi-reference graph framework with geodesic constraints, which enables computation of multidimensional representations, on a cell-by-cell basis, for functional enrichment and bioinformatics analysis. Here, we present a novel method, multi-reference graph cut (MRGC), for nuclear segmentation that overcomes technical variations associated with sample preparation by incorporating prior knowledge from manually annotated reference images and local image features. The proposed approach has been validated on manually annotated samples and then applied to a dataset of 377 Glioblastoma Multiforme (GBM) whole slide images from 146 patients. For the GBM cohort, multidimensional representation of the nuclear features and their organization have identified 1) statistically significant subtypes based on several morphometric indexes, 2) whether each subtype can be predictive or not, and 3) that the molecular correlates of predictive subtypes are consistent with the literature. Data and intermediaries for a number of tumor types (GBM, low grade glial, and kidney renal clear carcinoma) are available at: http://tcga.lbl.gov for correlation with TCGA molecular data. The website also provides an interface for panning and zooming of whole mount tissue sections with/without overlaid segmentation results- for quality control.
Keywords :
bioinformatics; cancer; cellular biophysics; feature extraction; image representation; image sampling; image segmentation; kidney; medical image processing; molecular biophysics; quality control; tumours; TCGA molecular data; The Cancer Genome Atlas; automated analysis; bioinformatics analysis; biological variation impede analysis; cell-by-cell basis; eosin; geodesic constraints; glioblastoma multiforme; hematoxylin; invariant delineation; kidney renal clear carcinoma; local image features; low grade glial; molecular association; molecular basis; morphometric indexes; mount tissue sections; multidimensional representations; multireference graph cut; multireference graph framework; neoplasm; nuclear architecture; nuclear segmentation; quality control; sample preparation; stained tissue sections; tumor histopathology; tumor subtypes; Bioinformatics; Computer architecture; Genomics; Image color analysis; Image segmentation; Laboratories; Tumors; Molecular pathology; nuclear segmentation; subtyping; tumor histopathology; Algorithms; Brain Neoplasms; Cell Nucleus; Coloring Agents; Databases, Factual; Eosine Yellowish-(YS); Fluorescent Dyes; Glioblastoma; Hematoxylin; Histocytochemistry; Humans; Staining and Labeling;
fLanguage :
English
Journal_Title :
Medical Imaging, IEEE Transactions on
Publisher :
ieee
ISSN :
0278-0062
Type :
jour
DOI :
10.1109/TMI.2012.2231420
Filename :
6374258
Link To Document :
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