Relational database structure to manage high-density tissue microarray data and images for pathology studies focusing on clinical outcome - The Prostate Specialized Program of Research Excellence Model

Citation
S. Manley et al., Relational database structure to manage high-density tissue microarray data and images for pathology studies focusing on clinical outcome - The Prostate Specialized Program of Research Excellence Model, AM J PATH, 159(3), 2001, pp. 837-843
Citations number
8
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology","Medical Research Diagnosis & Treatment
Journal title
AMERICAN JOURNAL OF PATHOLOGY
ISSN journal
00029440 → ACNP
Volume
159
Issue
3
Year of publication
2001
Pages
837 - 843
Database
ISI
SICI code
0002-9440(200109)159:3<837:RDSTMH>2.0.ZU;2-E
Abstract
With the completion of the Human Genome Project and high-throughput screeni ng methods using cDNA array and tissue microarray (TMA) technology, there i s a pressing need to manage the voluminous data sets generated from these t ypes of investigations. Herein is described a database model to handle 1) c linical and pathology data, 2) TMA location information, and 3) web-based h istology results. The model is useful for managing clinical, pathology, and molecular data on > 1300 prostate cancer patients dating back to 1995 from the University of Michigan Specialized Program of Research Excellence for prostate cancer. The key components in this multidatabase model are 1) the TMA database, 2) the TMA-image database (TMA-I DB), and 3) the prostate pat hology and clinical information databases. All databases were created in Mi crosoft Access (Microsoft, Redmond, WA). Desired patient, tissue, block, di agnosis, array location, and respective clinical and pathology information is obtained by linking the unique identifier fields among database tables. The TMA database is comprised of interrelated data from 336 prostate cancer patients transferred into 19 TMA blocks with 5451 TMA biopsy cores. Tissue samples include 1695 normal prostate, 3171 prostate cancer, 464 prostatic intraepithelial neoplasia, and 121 atrophy. All 19 TMA blocks have been ana lyzed over the Internet for several immunohistochemical biomarkers; includi ng E-cadherin, prostate-specific antigen, p27(Kip1), and Ki-67 labeling ind ex. This system facilitates the statistical analysis of high-density TMA da ta with clinical and pathology information in an efficient and cost-effecti ve manner. Because the review is performed over the Internet, this system i s ideal for collaborative multi-institutional studies.