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GNAQ mutation in a patient with metastatic mucosal melanoma
- Source :
- BMC Cancer
- Publication Year :
- 2014
- Publisher :
- BioMed Central, 2014.
-
Abstract
- Background Mucosal melanomas represent about 1% of all melanoma cases and classically have a worse prognosis than cutaneous melanomas. Due to the rarity of mucosal melanomas, only limited clinical studies with metastatic mucosal melanoma are available. Mucosal melanomas most commonly contain mutations in the gene CKIT, and treatments have been investigated using targeted therapy for this gene. Mutations in mucosal melanoma are less common than in cutaneous or uveal melanomas and occur in descending order of frequency as: CKIT (20%), NRAS (5%) or BRAF (3%). Mutations in G-alpha proteins, which are associated with activation of the mitogen-activated protein kinase pathway, have not been reported in mucosal melanomas. These G-alpha protein mutations occur in the genes GNAQ and GNA11 and are seen at a high frequency in uveal melanomas, those melanomas that begin in the eye. Case presentation A 59-year old Caucasian male was diagnosed with a mucosal melanoma after evaluation for what was thought to be a hemorrhoid. Molecular analysis of the tumor revealed a GNAQ mutation. Ophthalmologic exam did not disclose a uveal melanoma. Conclusion Here we report, to our knowledge, the first known case of GNAQ mutation in a patient with metastatic mucosal melanoma.
- Subjects :
- Neuroblastoma RAS viral oncogene homolog
Male
Pathology
medicine.medical_specialty
Cancer Research
medicine.medical_treatment
Case Report
medicine.disease_cause
Targeted therapy
GNAQ
Surgical oncology
Genetics
Medicine
Humans
Neoplasm Metastasis
neoplasms
Melanoma
Mutation
Mucous Membrane
GNA11
business.industry
Mucosal melanoma
Middle Aged
medicine.disease
GTP-Binding Protein alpha Subunits
Oncology
Cancer research
GTP-Binding Protein alpha Subunits, Gq-G11
business
Subjects
Details
- Language :
- English
- ISSN :
- 14712407
- Volume :
- 14
- Database :
- OpenAIRE
- Journal :
- BMC Cancer
- Accession number :
- edsair.doi.dedup.....1881324ab28d7b0d52237f73aac8fc7b