""""""""In breast cancer, vasoactive intestinal peptide (VIP) is an autocrine growth factor. High densities (100,000/cell) of VIP receptors are present in breast cancer cells. In the present period 18F-VIP conjugates were synthesized and evaluated for biological activity. The VIP conjugates bound with high affinity to T47D cells and elevated cAMP. Also, 18F-VIP localized to breast cancer tumors in nude mice. These results suggest that 18F-VIP may be a useful agent to localize breast cancer tumors using positron emission tomography techniques. Sigma receptors were characterized in breast cancer cells. Sigma ligands such as haloperidol bind to MCF-7 cells with high affinity (Kd = 10 nM). High concentrations of haloperidol (10 uM) elevate cytosolic Ca2++ in MCF-7 cells and inhibit their proliferation. Similar results were obtained for (2-piperidinyl-amino ethyl)-4-iodobenzamide (IPAB), N-(2-piperidino)ethyl)-4-iodobenzamide (4-IBP) and N-[2-(1'-piperidinyl)ethyl]-3-iodo-4-methoxy-benzamide (PIMBA). IPAB, 4-IBP or PIMBA inhibited T47D growth in vitro and breast tumor proliferation in nude mice. These results suggest that sigma ligands may be therapeutic agents for breast cancer.""""""""

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Intramural Research (Z01)
Project #
1Z01SC000201-04
Application #
6123627
Study Section
Special Emphasis Panel (M)
Project Start
Project End
Budget Start
Budget End
Support Year
4
Fiscal Year
1998
Total Cost
Indirect Cost
Name
National Cancer Institute Division of Clinical Sciences
Department
Type
DUNS #
City
State
Country
United States
Zip Code