During the 10 years the Colorado SPORE Tissue Bank Core Laboratory (TBC) has been in existence, two trends have increased the need for optimally processed and preserved specimens from lung cancer patients and subjects at risk for lung cancer. One is the increasing availability of treatment modalities that target specific molecular pathways, such as the ErbB pathway. The second is the shift in focus from clinically symptomatic and usually late stage lung cancers to asymptomatic and early stage or preinvasive lesions in high risk populations. Because of these trends, it has been increasingly important to assess the status of targeted pathways selected for treatment, to monitor the effects of new treatments on biology and prognosis and to define the detailed morphology and expected biological behavior of early lesions. For this work there is no more important tool than tumor or preneoplastic tissue itself. Observations in tumor tissue such as the identification of biomarkers may be extrapolated to more accessible fluid specimens such as blood, sputum, bronchoalveolar lavage fluid, urine and surrogate tissue. National panels charged with assessing the state of the science in lung cancer research have consistently identified lack of adequately preserved and studied tissue samples with clinical correlates as a continuing obstacle to the application and validation of promising molecular and imaging technology to the problem of lung cancer.
Specific aims of the TBC then are to: 1. provide well characterized tissues and products derived from those tissues to SPORE investigators 2. assess status of submitted specimens by histological and in situ analyses 3. link specimens to clhfical data including outcomes in rigid compliance with standards for maintenance of patient confidentiality and informed consent. To accomplish these aims the TBC has established innovative methods for the collection of samples for national and local trials and has become a central repository for the Southwest Oncology Group, the American College of Radiology Imaging Network (ACRIN), interSPORE chemoprevention trials and local SPORE detection, treatment and prevention trials. The TBC is a leader in the development of specimen preparation and preservation methods that are required for application of new technologies to tissue analysis. These include preparation of high quality RNA and DNA for microarray analyses, creation of a tissue mieroarray facility, and tissue culture methods to provide purified cell preparations for molecular and cytogenetic analyses. Most importantly, the maturation of the TBC has created a sufficiently large and longstanding resource that it is now possible to create case control scenarios that are of sufficient statistical power to support clinical hypothesis testing.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Specialized Center (P50)
Project #
2P50CA058187-09
Application #
6825291
Study Section
Special Emphasis Panel (ZCA1)
Project Start
2003-09-26
Project End
2008-04-30
Budget Start
Budget End
Support Year
9
Fiscal Year
2003
Total Cost
Indirect Cost
Name
University of Colorado Denver
Department
Type
DUNS #
065391526
City
Aurora
State
CO
Country
United States
Zip Code
80045
Noonan, Sinead A; Patil, Tejas; Gao, Dexiang et al. (2018) Baseline and On-Treatment Characteristics of Serum Tumor Markers in Stage IV Oncogene-Addicted Adenocarcinoma of the Lung. J Thorac Oncol 13:134-138
DeHart, David N; Fang, Diana; Heslop, Kareem et al. (2018) Opening of voltage dependent anion channels promotes reactive oxygen species generation, mitochondrial dysfunction and cell death in cancer cells. Biochem Pharmacol 148:155-162
Patil, Tejas; Smith, Derek E; Bunn, Paul A et al. (2018) The Incidence of Brain Metastases in Stage IV ROS1-Rearranged Non-Small Cell Lung Cancer and Rate of Central Nervous System Progression on Crizotinib. J Thorac Oncol 13:1717-1726
Suda, Kenichi; Kim, Jihye; Murakami, Isao et al. (2018) Innate Genetic Evolution of Lung Cancers and Spatial Heterogeneity: Analysis of Treatment-Naïve Lesions. J Thorac Oncol 13:1496-1507
Helfrich, Barbara A; Gao, Dexiang; Bunn Jr, Paul A (2018) Eribulin inhibits the growth of small cell lung cancer cell lines alone and with radiotherapy. Lung Cancer 118:148-154
Kleczko, Emily K; Heasley, Lynn E (2018) Mechanisms of rapid cancer cell reprogramming initiated by targeted receptor tyrosine kinase inhibitors and inherent therapeutic vulnerabilities. Mol Cancer 17:60
McCoach, Caroline E; Le, Anh T; Gowan, Katherine et al. (2018) Resistance Mechanisms to Targeted Therapies in ROS1+ and ALK+ Non-small Cell Lung Cancer. Clin Cancer Res 24:3334-3347
Drilon, Alexander; Laetsch, Theodore W; Kummar, Shivaani et al. (2018) Efficacy of Larotrectinib in TRK Fusion-Positive Cancers in Adults and Children. N Engl J Med 378:731-739
Pilling, Amanda B; Kim, Jihye; Estrada-Bernal, Adriana et al. (2018) ALK is a critical regulator of the MYC-signaling axis in ALK positive lung cancer. Oncotarget 9:8823-8835
Kwak, Jeff W; Laskowski, Jennifer; Li, Howard Y et al. (2018) Complement Activation via a C3a Receptor Pathway Alters CD4+ T Lymphocytes and Mediates Lung Cancer Progression. Cancer Res 78:143-156

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