In the presence of O6-Benzylguanine (06-BG) tumor cell lines have demonstrated an increased sensitivity to alkylating agents such as nitrosoureas and procarbazine. The mechanism proposed for this property of O6-BG is in part attributed to its ability to inactivate an important enzyme involved in DNA replication and repair pathways called alkylguanine-DNA alkyltransferase (AGT). The objectives of the study are the following: 7 To define a dose of O6-BG that depletes all AGT activity in >90% of the AA or GM cases evaluated. 7 To evaluate the associated toxicities both quantitatively and qualitatively. GCRC expertise would be used to administer the pre-surgical O6-BG administration and subsequently to provide consistent data with daily blood draws and toxicity notation.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
3M01RR000079-36S1
Application #
6115238
Study Section
Project Start
1998-12-01
Project End
1999-11-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
36
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Type
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
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Wang, Julie B; Pierce, John P; Ayala, Guadalupe X et al. (2015) Baseline Depressive Symptoms, Completion of Study Assessments, and Behavior Change in a Long-Term Dietary Intervention Among Breast Cancer Survivors. Ann Behav Med 49:819-27
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