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Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas 77030 [S. E. B., T. C. P., L. V. S., N. L. W.], and Departments of Urology and Biostatistics and Epidemiology, Memorial Sloan-Kettering Cancer Center, New York, New York 10021 [M. W. K.]
Limited options for the treatment of prostate cancer have spurred the
search for new therapies. One innovative approach is the use of
1
,25-dihydroxyvitamin D3 (calcitriol) analogues to
inhibit cancer growth. We demonstrate here that the calcitriol
analogue, EB1089, extensively inhibits the growth of LNCaP prostate
cancer cells in culture and causes the cells to both accumulate in
G0-G1 and undergo apoptosis. Importantly, we
found that EB1089 inhibits the growth of LNCaP tumor xenografts in nude
mice. Because of these antiproliferative properties in
vivo, EB1089 is a potential new therapeutic agent for the
treatment of prostate cancer.
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K. L. Burnstein, N. L. Weigel, S. E. Blutt, T. C. Polek, and L. V. Stewart Correspondence re: S. E. Blutt, T. C. Polek, L. V. Stewart, M. W. Kattan, and N. L. Weigel, A Calcitriol Analogue, EB1089, Inhibits the Growth of LNCaP Tumors in Nude Mice. Cancer Res., 60: 779-782, 2000. Cancer Res., May 1, 2001; 61(10): 4294 - 4294. [Full Text] |
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