Hedgehog (Hh) signaling has emerged in recent years as an attractive target for anticancer therapy because its aberrant activation is implicated in several cancers. Major progress has been made in the development of SMOOTHENED (SMO) antagonists, although they have shown several limitations due to downstream SMO pathway activation or the occurrence of drug-resistant SMO mutations. Recently, particular interest has been elicited by the identification of molecules able to hit glioma-associated oncogene (GLI) factors, the final effectors of the Hh pathway, which provide a valid tool to overcome anti-SMO resistance. Here, we review results achieved in developing GLI antagonists, explaining their mechanisms of action and highlighting their therapeutic potential. We also underline the relevance of structural details in their discovery and optimization.

Targeting GLI factors to inhibit the Hedgehog pathway / Infante, Paola; Alfonsi, Romina; Botta, Bruno; Mori, Mattia; DI MARCOTULLIO, Lucia. - In: TRENDS IN PHARMACOLOGICAL SCIENCES. - ISSN 0165-6147. - STAMPA. - 36:8(2015), pp. 547-558. [10.1016/j.tips.2015.05.006]

Targeting GLI factors to inhibit the Hedgehog pathway

INFANTE, PAOLA;ALFONSI, ROMINA;BOTTA, Bruno;MORI, MATTIA;DI MARCOTULLIO, LUCIA
2015

Abstract

Hedgehog (Hh) signaling has emerged in recent years as an attractive target for anticancer therapy because its aberrant activation is implicated in several cancers. Major progress has been made in the development of SMOOTHENED (SMO) antagonists, although they have shown several limitations due to downstream SMO pathway activation or the occurrence of drug-resistant SMO mutations. Recently, particular interest has been elicited by the identification of molecules able to hit glioma-associated oncogene (GLI) factors, the final effectors of the Hh pathway, which provide a valid tool to overcome anti-SMO resistance. Here, we review results achieved in developing GLI antagonists, explaining their mechanisms of action and highlighting their therapeutic potential. We also underline the relevance of structural details in their discovery and optimization.
2015
cancer; drug discovery; GLI antagonists; Hedgehog pathway; Animals; Antineoplastic Agents; Hedgehog Proteins; Humans; Receptors, G-Protein-Coupled; Signal Transduction; Transcription Factors; Pharmacology; Toxicology; Medicine (all)
01 Pubblicazione su rivista::01a Articolo in rivista
Targeting GLI factors to inhibit the Hedgehog pathway / Infante, Paola; Alfonsi, Romina; Botta, Bruno; Mori, Mattia; DI MARCOTULLIO, Lucia. - In: TRENDS IN PHARMACOLOGICAL SCIENCES. - ISSN 0165-6147. - STAMPA. - 36:8(2015), pp. 547-558. [10.1016/j.tips.2015.05.006]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/871963
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