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Design of Hedgehog pathway inhibitors for cancer treatment

期刊

MEDICINAL RESEARCH REVIEWS
卷 39, 期 3, 页码 1137-1204

出版社

WILEY
DOI: 10.1002/med.21555

关键词

cancer; cyclopamine; GDC-0449; Hedgehog inhibitor; nanomedicine; SMO; Smoothened; structure-activity relationship (SAR)

资金

  1. National Institute of Health [1RO1GM113166]
  2. University of Nebraska Medical Center

向作者/读者索取更多资源

Hedgehog (Hh) signaling is involved in the initiation and progression of various cancers and is essential for embryonic and postnatal development. This pathway remains in the quiescent state in adult tissues but gets activated upon inflammation and injuries. Inhibition of Hh signaling pathway using natural and synthetic compounds has provided an attractive approach for treating cancer and inflammatory diseases. While the majority of Hh pathway inhibitors target the transmembrane protein Smoothened (SMO), some small molecules that target the signaling cascade downstream of SMO are of particular interest. Substantial efforts are being made to develop new molecules targeting various components of the Hh signaling pathway. Here, we have discussed the discovery of small molecules as Hh inhibitors from the diverse chemical background. Also, some of the recently identified natural products have been included as a separate section. Extensive structure-activity relationship (SAR) of each chemical class is the focus of this review. Also, clinically advanced molecules are discussed from the last 5 to 7 years. Nanomedicine-based delivery approaches for Hh pathway inhibitors are also discussed concisely.

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