Deciphering the mystery of thalidomide teratogenicity
Article first published online: 21 FEB 2012
© 2011 The Authors. Congenital Anomalies © 2011 Japanese Teratology Society
Volume 52, Issue 1, pages 1–7, March 2012
How to Cite
Ito, T. and Handa, H. (2012), Deciphering the mystery of thalidomide teratogenicity. Congenital Anomalies, 52: 1–7. doi: 10.1111/j.1741-4520.2011.00351.x
- Issue published online: 21 FEB 2012
- Article first published online: 21 FEB 2012
- Accepted manuscript online: 1 DEC 2011 09:49AM EST
- Received October 30, 2011; revised and accepted November 23, 2011.
- ferrite-glycidyl methacrylate beads;
Thalidomide was originally developed in 1954 as a sedative that was commonly used to ameliorate morning sickness. However, thalidomide exposure during the first trimester of pregnancy caused multiple birth defects (e.g. phocomelia and amelia), affecting ∼10 000 children worldwide in the late 1950s and early 1960s. Thalidomide is now recognized as a clinically effective, albeit strictly restricted, drug for the treatment of leprosy and multiple myeloma. Investigators have studied thalidomide teratogenicity for half a century, proposing over 30 hypotheses to account for its actions. Among these, the anti-angiogenesis and oxidative stress models have gained widespread support. Nonetheless, the precise molecular mechanisms and direct targets of thalidomide have not heretofore been elucidated. We developed ferrite-glycidyl methacrylate beads that enable magnetic separation and efficient purification of ligand-binding molecules; the beads were recently employed to identify cereblon as a primary target of thalidomide. Cereblon forms an E3 ubiquitin ligase complex with DDB1, Cul4A, and Roc1, which is important for the expression of fibroblast growth factor 8, an essential regulator of limb development. Expression of a drug binding-deficient mutant of cereblon suppressed thalidomide-induced effects in zebrafish and chicks. This suggests that thalidomide downregulates fibroblast growth factor 8 expression and induces limb malformation by binding to wild-type cereblon, inhibiting the function of the associated E3 ubiquitin ligase. The present review summarizes the teratogenicity of thalidomide, including existing models for its mode of action, and discusses the identification of cereblon as a key molecule for deciphering the longstanding mystery of thalidomide teratogenicity.