The Clinical Tissue Procurement and Sequencing Core (CTPSC) is essential in providing support and resources for the Urologic Oncology Branch (UOB) and for our collaborators. It is the CTPSC's responsibility to handle every biospecimen that is generated within the UOB, to process each specimen in order to preserve biomolecules, to keep an accurate inventory of each procurement, and to assist in the scientific analysis of select specimens, for the ultimate goal of elucidating biological pathways relating to kidney, prostate, and bladder cancers. The CTPSC processes tissue from nearly 100% of UOB surgeries, as well as a subset of biopsies and other medical procedures. Typically, there are between two and five surgeries per week, resulting in surgical samples from about 100 patients procured per year, including kidney, prostate, and bladder carcinomas, adrenal tumors, uterine leiomyomas, lymph node metastases, pancreatic tumors, and other specimens relating to sporadic and familial urologic cancer syndromes. Tissue is always procured in cooperation with Surgical Pathology, to ensure proper handling and accurate diagnosis. Tissue is snap frozen, preserved in formalin or glutaraldehyde, or processed for biomolecule purification and analysis. In addition, blood samples are regularly taken from patients with inherited kidney cancer syndromes, in order to prepare DNA for analysis. Serum or plasma is also collected from select patients for analysis of proteins and other biomarkers. Ten to twenty blood samples may be processed per week. Frozen samples are stored in liquid nitrogen or a -80 degree centigrade freezer. All specimens are assigned a laboratory number and entered into a secure database, Labmatrix. In all, over 700 tissue and blood specimens have been procured within the last year. The entire UOB tissue repository contains in excess of 16,000 tissue samples and DNA from 1,200 blood samples from over 1,000 patients. Most of the samples were collected at the NIH Clinical Center, and full patient histories are incorporated into Labmatrix. Older samples currently in the FreezerWorks biorepository are also being entered promptly into Labmatrix, with the aim of completing the incorporation into Labmatrix within the next fiscal year. A future goal is for all clinical and laboratory findings to be incorporated into Labmatrix to provide an accessible resource for all of our studies from bench to bedside. A key function of the CTPSC is to support clinical trials in progress within the Branch. We are currently involved in two clinical trials: Glaxo GSK1363089 for patients with type 1 papillary kidney cancer, and AstraZeneca ZD6474 for patients with VHL or sporadic clear cell kidney cancer. Blood samples are processed weekly by the CTPSC, for the purpose of investigating pharmacodynamic (PD) and phamacokinetic (PK) effects of the drugs, as well as the study of other cancer biomarkers. In addition, in a collaborative effort with other laboratories to ascertain tumor histology, gene mutations, and chromosomal aberrations, we obtain and process tumor specimens from these patients. These studies are integral to the Glaxo GSK1363089 drug protocol. Many of the tumor samples from kidney cancer surgeries are procured under sterile conditions to establish new cell cultures and mouse xenografts. We have generated over 300 kidney cancer cell lines, 43 of which have been extensively characterized for cancer gene mutations. These include four lines generated from familial kidney cancer syndromes (BHD, SDHB, and 2 HLRCC lines) that provide unique reagents for studying the activity of these respective tumor suppressor genes. In the last year, approximately two dozen kidney tumors have been placed in cell culture and/or in SCID/BEIG or nude mice, with a subset of these growing viably in the short-term and a small number successfully established as immortal lines (six within the past year). These lines are invaluable for studying both the molecular basis of tumor development and prospective therapies. Cell lines are kept in standard carbon dioxide or low oxygen incubators or stored in liquid nitrogen, and mice are housed in an appropriate on-site facility. The Branch has also generated immortal B cell line samples from several hundred UOB patients from families with VHL, BHD, HPRC, HLRCC, or unknown familial kidney cancer syndromes. These lines provide an unlimited resource for germline DNA in order to characterize genetic aberrations of known genes of interest, as well as the potential to discover new genes that may involved in inherited kidney cancer in patients that have not yet been diagnosed. In addition, these lines provide the opportunity to study genes of interest at the RNA expression level. The collection of DNA samples for the detection and characterization of germline disease mutations has been at the heart of the gene discovery process in the UOB. Approximately 30 blood samples per year are analyzed by DNA sequencing, comparative genome hybridization (CGH) analysis, fluorescent in-situ hybridization (FISH), and other genetic studies. Furthermore, by using array CGH, we have performed fine mapping of 3 distinct germline deletions from HLRCC families and 61 distinct germline deletions from VHL families, with the goal of correlating the sizes and locations of these deletions with the severity of disease and/or response to clinical treatments. By combining array CGH with DNA sequencing on an ABI Prism 310 Gene Analyzer, we have mapped 47 VHL family deletions to the exact nucleotide (33 of these within the past year), for ultimate accuracy of characterization of their germline aberrations. We continue to use these techniques to discover new mutations, deletions, and amplifications. Both frozen and formalin-fixed tissues from kidney, prostate, and bladder cancers that have been processed by the CTPSC have been used extensively by the UOB for characterization using techniques such as immunohistochemistry, quantitative PCR, expression microarrays, Northern and Western blotting, immunoprecipitation, and DNA sequencing. Glutaraldehyde-fixed tissues have been used for electron microscopy, in order to characterize subcellular organelles. Proper handling of our surgical specimens has been an essential factor in assuring the best quality laboratory results. The UOB is involved in providing aliquots of many of its procured tumor tissues and blood samples to collaborating laboratories. The Branch has long-standing collaborations in which we distribute tissue to other laboratories for cell culture and immunotherapy for kidney cancer patients, analysis of kidney cancer stem cell markers, protein and RNA studies of adrenal masses (pheochromocytomas), and molecular epidemiology studies of prostate cancers. Serum and plasma from select kidney cancer and prostate cancer patients are being collected for molecular studies by other laboratories as well as ours. The sizeable biospecimen collection amassed by the UOB over the last 20 years provides an invaluable resource for both basic and clinical research regarding kidney, prostate and bladder cancers.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Scientific Cores Intramural Research (ZIC)
Project #
1ZICBC011044-02
Application #
7970014
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
2
Fiscal Year
2009
Total Cost
$353,655
Indirect Cost
Name
National Cancer Institute Division of Basic Sciences
Department
Type
DUNS #
City
State
Country
Zip Code
Li, Qingdi Quentin; Hsu, Iawen; Sanford, Thomas et al. (2018) Protein kinase D inhibitor CRT0066101 suppresses bladder cancer growth in vitro and xenografts via blockade of the cell cycle at G2/M. Cell Mol Life Sci 75:939-963
Peri, Suraj; Caretti, Elena; Tricarico, Rossella et al. (2017) Haploinsufficiency in tumor predisposition syndromes: altered genomic transcription in morphologically normal cells heterozygous for VHL or TSC mutation. Oncotarget 8:17628-17642
Hasumi, Hisashi; Hasumi, Yukiko; Baba, Masaya et al. (2017) H255Y and K508R missense mutations in tumour suppressor folliculin (FLCN) promote kidney cell proliferation. Hum Mol Genet 26:354-366
Vocke, Cathy D; Ricketts, Christopher J; Merino, Maria J et al. (2017) Comprehensive genomic and phenotypic characterization of germline FH deletion in hereditary leiomyomatosis and renal cell carcinoma. Genes Chromosomes Cancer 56:484-492
Yang, Youfeng; Vocke, Cathy D; Ricketts, Christopher J et al. (2017) Genomic and metabolic characterization of a chromophobe renal cell carcinoma cell line model (UOK276). Genes Chromosomes Cancer 56:719-729
Fei, Suzanne S; Mitchell, Asia D; Heskett, Michael B et al. (2016) Patient-specific factors influence somatic variation patterns in von Hippel-Lindau disease renal tumours. Nat Commun 7:11588
Sidana, Abhinav; Walton-Diaz, Annerleim; Truong, Hong et al. (2016) Postoperative elevation in creatine kinase and its impact on renal function in patients undergoing complex partial nephrectomy. Int Urol Nephrol 48:1047-1053
Schmidt, Laura S; Linehan, W Marston (2015) Molecular genetics and clinical features of Birt-Hogg-Dubé syndrome. Nat Rev Urol 12:558-69
Sourbier, Carole; Ricketts, Christopher J; Matsumoto, Shingo et al. (2014) Targeting ABL1-mediated oxidative stress adaptation in fumarate hydratase-deficient cancer. Cancer Cell 26:840-850
Shuch, Brian; Ricketts, Christopher J; Vocke, Cathy D et al. (2013) Adrenal nodular hyperplasia in hereditary leiomyomatosis and renal cell cancer. J Urol 189:430-5

Showing the most recent 10 out of 26 publications