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Hedgehog signaling in basal cell carcinoma
- Source :
- Journal of Dermatological Science. 78:95-100
- Publication Year :
- 2015
- Publisher :
- Elsevier BV, 2015.
-
Abstract
- Basal cell carcinoma (BCC), the most common type of skin cancer, is occasionally aggressive with deep invasion, destruction of adjacent structures, recurrence and, on very rare occasions, regional and distant metastases. Mutations that occur in BCC in hedgehog (Hh) pathway genes primarily involve the genes encoding patched homolog (PTCH) and smoothened homolog (SMO). Several animal models have demonstrated the functional relevance of genetic alterations in the Hh pathway during tumorigenesis. Recently, targeted therapy has become available both commercially and in the context of human clinical trials. Interestingly, Hh pathway inhibitors not only suppress BCC progression but also promote acquired immune responses. Since immune responses are crucial for long-term tumor control, new clinical trials, such as those involving a combination of Hh inhibitors with immune modifiers, are needed to supplement standard methods of tumor control.
- Subjects :
- Patched Receptors
Patched
Pathology
medicine.medical_specialty
1303 Biochemistry
Skin Neoplasms
Pyridines
medicine.medical_treatment
610 Medicine & health
Antineoplastic Agents
Receptors, Cell Surface
Context (language use)
Dermatology
Adaptive Immunity
Biology
medicine.disease_cause
Biochemistry
Receptors, G-Protein-Coupled
Targeted therapy
2708 Dermatology
1312 Molecular Biology
medicine
Animals
Humans
Anilides
Hedgehog Proteins
Basal cell carcinoma
Molecular Targeted Therapy
Molecular Biology
Hedgehog
10177 Dermatology Clinic
medicine.disease
Smoothened Receptor
Hedgehog signaling pathway
Smoothened Homolog
Patched-1 Receptor
Carcinoma, Basal Cell
Cancer research
Carcinogenesis
Signal Transduction
Subjects
Details
- ISSN :
- 09231811
- Volume :
- 78
- Database :
- OpenAIRE
- Journal :
- Journal of Dermatological Science
- Accession number :
- edsair.doi.dedup.....6d17c0a9d33b1856a8c2d0c8bfedb60c
- Full Text :
- https://doi.org/10.1016/j.jdermsci.2015.02.007