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AuthorMarkota Cagalj, Adela
AuthorGlibo, Mislav
AuthorKarin-Kujundzic, Valentina
AuthorSerman, Alan
AuthorVranic, Semir
AuthorSerman, Ljiljana
AuthorSkara Abramovic, Lucija
AuthorBukvic Mokos, Zrinka
Available date2025-05-27T05:41:21Z
Publication Date2025
Publication NameJournal of Drug Targeting
ResourceScopus
Identifierhttp://dx.doi.org/10.1080/1061186X.2025.2496470
ISSN1061186X
URIhttp://hdl.handle.net/10576/65201
AbstractBasal cell carcinoma (BCC) is the most common type of skin cancer that usually appears in sun-exposed body regions such as the head, trunk, and extremities. There are four main clinicopathological subtypes of BCC: nodular, superficial, morpheaform, and fibroepithelial. BCC's molecular basis includes inherited genetic susceptibility and somatic mutations, often induced by exposure to UV radiation. The aberrant activation of the hedgehog (Hh) signalling pathway, caused by mutations in the Hh components, plays a central role in the molecular pathogenesis of this carcinoma. This led to the development of Hh signalling pathway inhibitors as a new treatment option for patients with advanced disease. In this review, we summarise BCC's clinical presentation and histopathology and present knowledge on the most studied Hh signalling inhibitors, vismodegib and sonidegib, and other inhibitors of this signalling, such as itraconazole, patidegib, taladegib, and arsenic trioxide, in the treatment of BCC. We also present the most common Hh signalling inhibitor adverse events and their management options, which could improve patients' quality of life during treatment.
Languageen
PublisherTaylor and Francis Ltd.
SubjectBasal cell carcinoma
GLI inhibitors
hedgehog signalling pathway
SMO inhibitors
sonidegib
vismodegib
TitleHedgehog signalling pathway inhibitors in the treatment of basal cell carcinoma: an updated review
TypeArticle Review
dc.accessType Full Text


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