The purpose of this award is the development of a physician scientist in cancer pharmacology. The candidate has demonstrated a potential to contribute to clinical urologic oncology and is committed to an academic career. However, he lacks formal basic science training. The sponsor is a recognized cancer researcher with an established record for training physicians in a basic science environment. The proposed investigation of metallothionein (MT) and cytotoxic drug resistance seeks to train a clinician in the discipline of molecular biology, pharmacology, and experimental therapeutics and to identify new strategies to overcome tumor resistance to chemotherapy. The research proposal is designed to investigate the role of MT in conferring resistance to cis-platin (cDDP) and related anti-cancer agents. cDDP is active against a variety of human tumors and is believed to act by forming covalent cross links in chromosomal DNA. Unfortunately, the development of resistance by tumor cells limits the therapeutic usefulness of cDDP. MT, a cysteine rich protein that protects cells against heavy metal toxicity, is an important candidate to modulate cellular response to cytotoxic drugs, especially those reactive with sulfhydryl groups. We will examine the elevation of MT in drug resistant cell lines utilizing enzyme linked immunosorbent assay (ELISA) using antibodies against MT. Since human MT exists in several isomeric forms, monoclonal antibodies specific for each human isoform will be developed and ELISA will be used to examine if drug-resistant cell lines exhibit increases in any particular isoform of MT. In addition, the sensitivity to cDDP will be determined in cells with MT levels manipulated by established inducers of MT. The mechanism of over expression of MT will be studied by characterizing the MT gene copy number, mRNA level and stability of message of MT. Finally, mRNA and protein levels of MT will be determined in tissue samples from patients with urologic malignancy to evaluate if MT influences responsiveness to cDDP and whether cDDP alters human tumor expression of MT. The University of Pittsburgh is particularly well suited for the development of physician investigators in oncology because of its Pittsburgh Cancer Institute which was recently awarded a Cancer Center Support Grant for three years from the NIH.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Clinical Investigator Award (CIA) (K08)
Project #
5K08CA001490-04
Application #
3079970
Study Section
Cancer Institutional Fellowship Review Committee (CT)
Project Start
1990-07-01
Project End
1995-06-30
Budget Start
1993-07-01
Budget End
1994-06-30
Support Year
4
Fiscal Year
1993
Total Cost
Indirect Cost
Name
University of Pittsburgh
Department
Type
Schools of Medicine
DUNS #
053785812
City
Pittsburgh
State
PA
Country
United States
Zip Code
15213
Schwartz, G G; Hill, C C; Oeler, T A et al. (1995) 1,25-Dihydroxy-16-ene-23-yne-vitamin D3 and prostate cancer cell proliferation in vivo. Urology 46:365-9
Bahnson, R R; Smith, D; Trump, D (1995) Adjuvant chemotherapy for bladder cancer. Standard of care or unproven therapy? Surg Oncol Clin N Am 4:287
Glazier, D B; Bahnson, R R; McLeod, D G et al. (1995) Intravesical recombinant tumor necrosis factor in the treatment of superficial bladder cancer: an Eastern Cooperative Oncology Group study. J Urol 154:66-8
Bennett, B C; Selby, R; Bahnson, R R (1995) Surgical resection for management of renal cancer with hepatic involvement. J Urol 154:972-4
Agarwala, S S; Bahnson, R R; Wilson, J W et al. (1995) Evaluation of the combination of vinblastine and quinidine in patients with metastatic renal cell carcinoma. A phase I study. Am J Clin Oncol 18:211-5
Schwartz, G G; Oeler, T A; Uskokovic, M R et al. (1994) Human prostate cancer cells: inhibition of proliferation by vitamin D analogs. Anticancer Res 14:1077-81
Corral, D A; Bahnson, R R (1994) Survival of men with clinically localized prostate cancer detected in the eighth decade of life. J Urol 151:1326-9
Bahnson, R R; Becich, M; Ernstoff, M S et al. (1994) Absence of immunohistochemical metallothionein staining in bladder tumor specimens predicts response to neoadjuvant cisplatin, methotrexate and vinblastine chemotherapy. J Urol 152:2272-5
Yang, Y Y; Woo, E S; Reese, C E et al. (1994) Human metallothionein isoform gene expression in cisplatin-sensitive and resistant cells. Mol Pharmacol 45:453-60
Corral, D A; Bahnson, R R (1993) Recurrent transitional cell carcinoma in an ileal conduit treated by sandwich chemotherapy and surgical resection. J Urol 150:471-2

Showing the most recent 10 out of 16 publications