Bisphosphonamidate Clodronate Prodrug Exhibits Potent Anticancer Activity in Non-Small-Cell Lung Cancer Cells
摘要:
Bisphoshonates are used clinically to treat disorders of calcium metabolism, hypercalcemia and osteoporosis, and malignant bone disease. Although these agents are commonly used in cancer patients and have potential direct anticancer effects, their use for the treatment of extraskeletal disease is limited as a result of poor cellular uptake. We have designed and synthesized bisphosphonamidate prodrugs that undergo intracellular activation to release the corresponding bisphosphonate and require only two enzymatic activation events to unmask multiple negative charges. We demonstrate efficient bisphosphonamidate activation and significant enhancement in anticancer activity of two bisphosphonamidate prodrugs in vitro compared to the parent bisphosphonate. These data suggest a novel approach to optimizing the anticancer activities of commonly used bisphosphonates.
[EN] BISPHOSPHONAMIDATE PRODRUGS AND USES THEREOF<br/>[FR] PROMÉDICAMENTS BISPHOSPHONAMIDATE ET LEURS UTILISATIONS
申请人:UNIV JOHNS HOPKINS
公开号:WO2011139791A3
公开(公告)日:2012-03-29
BISPHOSPHONAMIDATE PRODRUGS AND USES THEREOF
申请人:Freel Meyers Caren Laura
公开号:US20130090311A1
公开(公告)日:2013-04-11
Bisphosphonamidate prodrugs of therapeutic bisphosphonate compounds and uses thereof to treat diseases are described.
US8772268B2
申请人:——
公开号:US8772268B2
公开(公告)日:2014-07-08
Bisphosphonamidate Clodronate Prodrug Exhibits Potent Anticancer Activity in Non-Small-Cell Lung Cancer Cells
作者:Marie R. Webster、Ming Zhao、Michelle A. Rudek、Christine L. Hann、Caren L. Freel Meyers
DOI:10.1021/jm200521a
日期:2011.10.13
Bisphoshonates are used clinically to treat disorders of calcium metabolism, hypercalcemia and osteoporosis, and malignant bone disease. Although these agents are commonly used in cancer patients and have potential direct anticancer effects, their use for the treatment of extraskeletal disease is limited as a result of poor cellular uptake. We have designed and synthesized bisphosphonamidate prodrugs that undergo intracellular activation to release the corresponding bisphosphonate and require only two enzymatic activation events to unmask multiple negative charges. We demonstrate efficient bisphosphonamidate activation and significant enhancement in anticancer activity of two bisphosphonamidate prodrugs in vitro compared to the parent bisphosphonate. These data suggest a novel approach to optimizing the anticancer activities of commonly used bisphosphonates.