John Wayne Cancer Institute's (JWCI) polyvalent melanoma cell vaccine (PMCV) consists of three allogeneic melanoma cell lines selected from over fifty of such harvests in 1984. The following criteria melanoma cell lines: 1) they express different MHC Class I antigens, and 2) they contain immunogenic melanoma-associated antigens (MAA) GM2 and GD2. Over the past eleven years, we have utilized these cell lines in several Phase I and II clinical studies of active specific immunotherapy in patients with metastatic melanoma. Vaccine comprised of these lines has proven to be safe and have a therapeutic effect when compared to the natural history control patients treated at JWCI. The past decade has seen the continued discovery of new immunogenic antigens/epitopes expressed by malanoma and the assessment of their therapeutic applicability at molecular, immunological and clinical levels. JWCI's PMCV expresses at least sixteen of MAA known to elicit immune responses in man. Project I will evaluate antibody responses to these specific antigens in order to determine which of the antigen are relevant to disease regression following active specific immunotherapy with PMCV.
The specific aims are: 1) HuMAb will be developed to melanoma-associated recombinant or synthetic protein antigens; 2) epitopes for these antibodies will be determined; 3) binding specificity of antibodies for cancer tissues will be assessed; and 4) anti-tumor activity of antibodies will be tested in vitro and in vivo.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA012582-28
Application #
6101487
Study Section
Project Start
1999-02-01
Project End
2000-01-31
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
28
Fiscal Year
1999
Total Cost
Indirect Cost
Name
John Wayne Cancer Institute
Department
Type
DUNS #
556074458
City
Santa Monica
State
CA
Country
United States
Zip Code
90404
Dükel, Muzaffer; Streitfeld, W Scott; Tang, Tsz Ching Chloe et al. (2016) The Breast Cancer Tumor Suppressor TRIM29 Is Expressed via ATM-dependent Signaling in Response to Hypoxia. J Biol Chem 291:21541-21552
Kiyohara, Eiji; Hata, Keisuke; Lam, Stella et al. (2014) Circulating tumor cells as prognostic biomarkers in cutaneous melanoma patients. Methods Mol Biol 1102:513-22
Greenberg, Edward S; Chong, Kelly K; Huynh, Kelly T et al. (2014) Epigenetic biomarkers in skin cancer. Cancer Lett 342:170-7
Chiu, Connie G; Nakamura, Yoshitaka; Chong, Kelly K et al. (2014) Genome-wide characterization of circulating tumor cells identifies novel prognostic genomic alterations in systemic melanoma metastasis. Clin Chem 60:873-85
Faries, Mark B; Steen, Shawn; Ye, Xing et al. (2013) Late recurrence in melanoma: clinical implications of lost dormancy. J Am Coll Surg 217:27-34; discussion 34-6
Leung, Anna M; Hari, Danielle M; Morton, Donald L (2012) Surgery for distant melanoma metastasis. Cancer J 18:176-84
Kidner, Travis B; Morton, Donald L; Lee, Delphine J et al. (2012) Combined intralesional Bacille Calmette-Guérin (BCG) and topical imiquimod for in-transit melanoma. J Immunother 35:716-20
Hoshimoto, Sojun; Shingai, Tatsushi; Morton, Donald L et al. (2012) Association between circulating tumor cells and prognosis in patients with stage III melanoma with sentinel lymph node metastasis in a phase III international multicenter trial. J Clin Oncol 30:3819-26
Hoshimoto, Sojun; Kuo, Christine T; Chong, Kelly K et al. (2012) AIM1 and LINE-1 epigenetic aberrations in tumor and serum relate to melanoma progression and disease outcome. J Invest Dermatol 132:1689-97
Faries, Mark B; Morton, Donald L (2012) Staging of regional nodes in pulmonary malignancies. Ann Surg Oncol 19:703-5

Showing the most recent 10 out of 238 publications