This goal of this application is to establish a Biomarker Validation laboratory (BVL) at the University of Alabama at Birmingham, which will provide both the expertise and sufficient quantities of high quality resources to act as an efficient referral center within the Early Detection Research Network (EDRN) of the NCI. The P.I. Investigator, William B. Grizzle, MD, PhD, has assembled a group of investigators with expertise in biomarker evaluation and with a commitment to translational research. The UAB-BVL will offer a broad range of validation systems, as indicated in the RFA, and clinical and research expertise in tumors of various organ systems, including breast, prostate, colorecturn, lung, head and neck, and gynecologic. The major focus of the UAB-BVL will fulfill the requests for the development of well-characterized tissue resources, including urine and serum, that have been collected and stored according to standard procedures; the development of high through-put immunohistochemical techniques that have been characterized according to specificity, sensitivity, and reproducibility; and the molecular characterization of lesions that are currently defined histologically or morphologically. A Development Proposal entitled Molecular Markers to Characterize Aggressive PIN lesions addresses the issue of molecular characterization of PIN lesions in prostate cancer using tissue matrix technology. The BVL leverages the considerable expertise of the investigators and will provide access to established tissue resources, standard operating procedures, and quality control systems as well as equipment. The Core Facilities of the UAB Comprehensive Cancer Center together with other Centers of Excellence at UAB further enhances the available resources. The existing collaborations among the investigators at UAB and the associated institutions and prior participation in national networks (CHTN, EDRN) will ensure rapid and effective responses to the needs of the EDRN. An organizational structure has been developed that defines lines of authority and communication to ensure both high quality performance and effective and timely communication. The research objectives of all of the investigators in this proposal match those of the EDRN: to rapidly translate basic research findings into a full understanding of the pathogenesis of neoplasia such that cancer patients can benefit from early detection, improved prognostic tools, and rapid development of more effective therapeutic and preventive strategies through the use of surrogate end- point markers.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Resource-Related Research Projects--Cooperative Agreements (U24)
Project #
5U24CA086359-03
Application #
6514559
Study Section
Special Emphasis Panel (ZCA1-SRRB-Y (J2))
Program Officer
Srivastava, Sudhir
Project Start
2000-03-27
Project End
2005-02-28
Budget Start
2002-05-03
Budget End
2003-02-28
Support Year
3
Fiscal Year
2002
Total Cost
$855,137
Indirect Cost
Name
University of Alabama Birmingham
Department
Pathology
Type
Schools of Medicine
DUNS #
004514360
City
Birmingham
State
AL
Country
United States
Zip Code
35294
Zhang, H-G; Zhuang, X; Sun, D et al. (2012) Exosomes and immune surveillance of neoplastic lesions: a review. Biotech Histochem 87:161-8
Johnson-Holiday, Crystal; Singh, Rajesh; Johnson, Erica et al. (2011) CCL25 mediates migration, invasion and matrix metalloproteinase expression by breast cancer cells in a CCR9-dependent fashion. Int J Oncol 38:1279-85
Johnson-Holiday, Crystal; Singh, Rajesh; Johnson, Erica L et al. (2011) CCR9-CCL25 interactions promote cisplatin resistance in breast cancer cell through Akt activation in a PI3K-dependent and FAK-independent fashion. World J Surg Oncol 9:46
Zhang, Huang-Ge; Grizzle, William E (2011) Exosomes and cancer: a newly described pathway of immune suppression. Clin Cancer Res 17:959-64
Bell, Walter C; Sexton, Katherine C; Grizzle, William E (2010) Organizational issues in providing high-quality human tissues and clinical information for the support of biomedical research. Methods Mol Biol 576:1-30
Shanmugam, Chandrakumar; Jhala, Nirag C; Katkoori, Venkat R et al. (2010) Prognostic value of mucin 4 expression in colorectal adenocarcinomas. Cancer 116:3577-86
Grizzle, William E; Srivastava, Sudhir; Manne, Upender (2010) The biology of incipient, pre-invasive or intraepithelial neoplasia. Cancer Biomark 9:21-39
Grizzle, William E; Bell, Walter C; Sexton, Katherine C (2010) Issues in collecting, processing and storing human tissues and associated information to support biomedical research. Cancer Biomark 9:531-49
Johnson, Erica L; Singh, Rajesh; Singh, Shailesh et al. (2010) CCL25-CCR9 interaction modulates ovarian cancer cell migration, metalloproteinase expression, and invasion. World J Surg Oncol 8:62
Srivastava, Sudhir; Grizzle, William E (2010) Biomarkers and the genetics of early neoplastic lesions. Cancer Biomark 9:41-64

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