TY - JOUR KW - Angiogenesis Inhibitors KW - Animals KW - Chick Embryo KW - Chickens KW - Lenalidomide KW - Neovascularization, Physiologic KW - Neurites KW - Neurotoxins KW - Species Specificity KW - Teratogens KW - Thalidomide KW - Zebrafish AU - Mahony C AU - Erskine L AU - Niven J AU - Greig NH AU - Figg WD AU - Vargesson N AB -

Thalidomide and its analog, Lenalidomide, are in current use clinically for treatment of multiple myeloma, complications of leprosy and cancers. An additional analog, Pomalidomide, has recently been licensed for treatment of multiple myeloma, and is purported to be clinically more potent than either Thalidomide or Lenalidomide. Using a combination of zebrafish and chicken embryos together with in vitro assays we have determined the relative anti-inflammatory activity of each compound. We demonstrate that in vivo embryonic assays Pomalidomide is a significantly more potent anti-inflammatory agent than either Thalidomide or Lenalidomide. We tested the effect of Pomalidomide and Lenalidomide on angiogenesis, teratogenesis, and neurite outgrowth, known detrimental effects of Thalidomide. We found that Pomalidomide, displays a high degree of cell specificity, and has no detectable teratogenic, antiangiogenic or neurotoxic effects at potent anti-inflammatory concentrations. This is in marked contrast to Thalidomide and Lenalidomide, which had detrimental effects on blood vessels, nerves, and embryonic development at anti-inflammatory concentrations. This work has implications for Pomalidomide as a treatment for conditions Thalidomide and Lenalidomide treat currently.

BT - Proceedings of the National Academy of Sciences of the United States of America C1 - http://www.ncbi.nlm.nih.gov/pubmed/23858438?dopt=Abstract CN - MAHONY2013 DA - 2013 Jul 30 DO - 10.1073/pnas.1307684110 IS - 31 J2 - Proc. Natl. Acad. Sci. U.S.A. LA - eng N2 -

Thalidomide and its analog, Lenalidomide, are in current use clinically for treatment of multiple myeloma, complications of leprosy and cancers. An additional analog, Pomalidomide, has recently been licensed for treatment of multiple myeloma, and is purported to be clinically more potent than either Thalidomide or Lenalidomide. Using a combination of zebrafish and chicken embryos together with in vitro assays we have determined the relative anti-inflammatory activity of each compound. We demonstrate that in vivo embryonic assays Pomalidomide is a significantly more potent anti-inflammatory agent than either Thalidomide or Lenalidomide. We tested the effect of Pomalidomide and Lenalidomide on angiogenesis, teratogenesis, and neurite outgrowth, known detrimental effects of Thalidomide. We found that Pomalidomide, displays a high degree of cell specificity, and has no detectable teratogenic, antiangiogenic or neurotoxic effects at potent anti-inflammatory concentrations. This is in marked contrast to Thalidomide and Lenalidomide, which had detrimental effects on blood vessels, nerves, and embryonic development at anti-inflammatory concentrations. This work has implications for Pomalidomide as a treatment for conditions Thalidomide and Lenalidomide treat currently.

PY - 2013 SP - 12703 EP - 8 T2 - Proceedings of the National Academy of Sciences of the United States of America TI - Pomalidomide is nonteratogenic in chicken and zebrafish embryos and nonneurotoxic in vitro. UR - http://www.pnas.org/content/early/2013/07/11/1307684110.long VL - 110 SN - 1091-6490 ER -