학술논문

Mutational Profile of GNAQQ209 in Human Tumors.
Document Type
Article
Source
PLoS ONE. 2009, Vol. 4 Issue 8, p1-4. 4p. 3 Charts, 1 Graph.
Subject
*GENETIC mutation
*ENDOCRINE glands
*TUMORS
*EXOCRINE glands
*URINARY organs
*MEMBRANE proteins
*ONCOLOGY
*MELANOMA
*CYSTS (Pathology)
*LEUCOCYTOSIS
Language
ISSN
1932-6203
Abstract
Background: Frequent somatic mutations have recently been identified in the ras-like domain of the heterotrimeric G protein α-subunit (GNAQ) in blue naevi 83%, malignant blue naevi (50%) and ocular melanoma of the uvea (46%). The mutations exclusively affect codon 209 and result in GNAQ constitutive activation which, in turn, acts as a dominant oncogene. Methodology: To assess if the mutations are present in other tumor types we performed a systematic mutational profile of the GNAQ exon 5 in a panel of 922 neoplasms, including glioblastoma, gastrointestinal stromal tumors (GIST), acute myeloid leukemia (AML), blue naevi, skin melanoma, bladder, breast, colorectal, lung, ovarian, pancreas, and thyroid carcinomas. Principal Findings: We detected the previously reported mutations in 6/13 (46%) blue naevi. Changes affecting Q209 were not found in any of the other tumors. Our data indicate that the occurrence of GNAQ mutations display a unique pattern being present in a subset of melanocytic tumors but not in malignancies of glial, epithelial and stromal origin analyzed in this study. [ABSTRACT FROM AUTHOR]