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Updated: Feb 13, 2026

Quantitative PCR-based Assay to Measure Sonic Hedgehog Signaling in Cellular Model of Ciliogenesis
Published on: January 31, 2025
A highlight on Sonic hedgehog pathway
Gabriela Basile Carballo1,2, Jéssica Ribeiro Honorato1,3,2, Giselle Pinto Farias de Lopes3
1Laboratorio de Biomedicina do Cérebro, Instituto Estadual do Cérebro Paulo Niemeyer (IECPN), Secretaria de Estado de Saúde, Rua do Rezende 156, Centro, Rio de Janeiro, CEP: 20230-024, Brazil.
The Sonic hedgehog (Shh) signaling pathway is crucial in brain tumor development and resistance to cancer therapies. Understanding Shh signaling offers new therapeutic targets for brain cancers.
Area of Science:
- Oncology
- Molecular Biology
- Developmental Biology
Background:
- The Hedgehog (Hh) signaling pathway is vital in embryonic development and cancer.
- Sonic hedgehog (Shh) pathway activation contributes to radio- and chemo-resistance in various tumors.
- Brain tumors often exhibit resistance to chemotherapy, leading to poor patient outcomes.
Purpose of the Study:
- To explore the role of the Shh signaling pathway in brain tumorigenesis.
- To identify potential therapeutic strategies targeting the Shh pathway for brain cancer treatment.
- To review current clinical trials investigating Shh pathway inhibitors.
Main Methods:
- Literature review of studies on Shh signaling in brain tumors.
- Analysis of Shh pathway interactions with other signaling cascades.
- Examination of data from ongoing clinical trials targeting Shh.
Main Results:
- Shh signaling influences the development and drug resistance of brain tumors.
- The pathway interacts with other molecular pathways implicated in tumorigenesis.
- Several clinical trials are evaluating Shh inhibitors for brain cancer therapy.
Conclusions:
- Targeting the Shh signaling pathway presents a promising therapeutic avenue for brain cancers.
- A comprehensive understanding of Shh signaling mechanisms can lead to novel treatment strategies.
- Further research and clinical trials are essential to fully exploit Shh pathway inhibitors.
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