The structure/function relationship is fundamental to our understanding of biological systems at all levels, and drives most, if not all, techniques for detecting, diagnosing, and treating disease. The concept is powerful enough to have inspired a 200+ year-long effort to describe the components of our biological universe in ever finer detail, beginning with the Linnean taxonomic system of cataloging organisms based on their structural similarities, and culminating with microscale descriptions such as the complete genomes of several organisms, including humans. However, having reduced the complex biological universe to a myriad of minute parts, we encounter new forms of complexity: data overload and curse of dimensionality. Simply put, we've taken our biological machine apart but can't put it back together again- our ability to accumulate reductionist data has outstripped our ability to understand it. Thus, we encounter a gap in the structure/function relationship: having accumulated an extraordinary amount of detailed information about biological structures, we can't assemble it in a way that explains the correspondingly complex biological functions these structures perform. We propose a novel approach to this problem based on representing tissues using graph theory and learning its structural properties by analyzing the underlying graphs. Our long-range objective is to close this gap by establishing quantitative features that link tissue structure to biological function. Our immediate goals for this project are to define three quantitatively different functional states (healthy, damaged, diseased) of three morphologically distinct tissues (brain, breast, bone) based on their distinguishing morphological characteristics, then test three hypotheses that propose to link these quantitative features to specific biological activities in these tissues Successful completion of this project will provide a new and powerful tool for quantitatively linking telltale structural properties of tissues (e.g., cellular distribution, morphology, contact) with specific disease states and fundamental behaviors of the cells comprising these tissues. This will be useful both to scientists conducting basic research to uncover the guiding principles of tissue structure and function, and to clinicians seeking to quickly and accurately detect and diagnose diseases that involve alterations in tissue structure.

Public Health Relevance

Successful completion of this project will provide a new and powerful tool for quantitatively linking telltale structural properties of tissues (e.g., cellular distribution, morphology, contact) with specific disease states and fundamental behaviors of the cells comprising these tissues. This will be useful both to scientists conducting basic research to uncover the guiding principles of tissue structure and function, and to clinicians seeking to quickly and accurately detect and diagnose diseases that involve alterations in tissue structure.

Agency
National Institute of Health (NIH)
Institute
National Institute of Biomedical Imaging and Bioengineering (NIBIB)
Type
Research Project (R01)
Project #
5R01EB008016-04
Application #
8072085
Study Section
Biodata Management and Analysis Study Section (BDMA)
Program Officer
Luo, James
Project Start
2008-07-15
Project End
2014-04-30
Budget Start
2011-05-01
Budget End
2014-04-30
Support Year
4
Fiscal Year
2011
Total Cost
$438,149
Indirect Cost
Name
Rensselaer Polytechnic Institute
Department
Biostatistics & Other Math Sci
Type
Schools of Arts and Sciences
DUNS #
002430742
City
Troy
State
NY
Country
United States
Zip Code
12180
Dhulekar, Nimit; Ray, Shayoni; Yuan, Daniel et al. (2016) Prediction of Growth Factor-Dependent Cleft Formation During Branching Morphogenesis Using A Dynamic Graph-Based Growth Model. IEEE/ACM Trans Comput Biol Bioinform 13:350-64
McKeen Polizzotti, Lindsey; Oztan, Basak; Bjornsson, Chris S et al. (2012) Novel image analysis approach quantifies morphological characteristics of 3D breast culture acini with varying metastatic potentials. J Biomed Biotechnol 2012:102036
Acar, Evrim; Plopper, George E; Yener, Bulent (2012) Coupled analysis of in vitro and histology tissue samples to quantify structure-function relationship. PLoS One 7:e32227
Bilgin, Cemal Cagatay; Ray, Shayoni; Baydil, Banu et al. (2012) Multiscale feature analysis of salivary gland branching morphogenesis. PLoS One 7:e32906
McKeen-Polizzotti, Lindsey; Henderson, Kira M; Oztan, Basak et al. (2011) Quantitative metric profiles capture three-dimensional temporospatial architecture to discriminate cellular functional states. BMC Med Imaging 11:11
Bilgin, Cemal Cagatay; Lund, Amanda W; Can, Ali et al. (2010) Quantification of three-dimensional cell-mediated collagen remodeling using graph theory. PLoS One 5:
Bilgin, Cemal Cagatay; Bullough, Peter; Plopper, George E et al. (2009) ECM-Aware Cell-Graph Mining for Bone Tissue Modeling and Classification. Data Min Knowl Discov 20:416-438
Lund, A W; Bilgin, C C; Hasan, M A et al. (2009) Quantification of spatial parameters in 3D cellular constructs using graph theory. J Biomed Biotechnol 2009:928286