Differential gene expression in melanocytic nevi with the V600E BRAF mutation
✍ Scribed by Sandra Bloethner; Erna Snellman; Justo Lorenzo Bermejo; Eva Hiripi; Andreas Gast; Ranjit K. Thirumaran; Ruth Wellenreuther; Kari Hemminki; Rajiv Kumar
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 278 KB
- Volume
- 46
- Category
- Article
- ISSN
- 1045-2257
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
We studied gene expression in 18 melanocytic nevi with and four nevi without the V600E mutation in the BRAF gene using HG‐U133A 2.0 microarray with 22,277 transcripts. Data analysis revealed 92 genes up‐regulated and 105 genes down‐regulated in nevi with the mutation compared to nevi without mutation. Pathway analysis showed that differentially regulated genes mapped to 10 genetic networks. The major network included genes involved in cell death, cell cycle, and cellular growth and proliferation. Up‐regulated genes in nevi with the mutation included CDKN2A, CDKN1C, and MITF; whereas down‐regulated genes included those involved in apoptotic and other pathways. Principal component analysis identified 22 probe sets (20 genes) that caused separate segregation of nevi with and without mutations. In conclusion, our data showed differences in gene expression between nevi with and without the V600E BRAF mutation. Moreover, nevi with mutations showed over‐expression of genes involved in melanocytic senescence and cell cycle inhibition. © 2007 Wiley‐Liss, Inc.
📜 SIMILAR VOLUMES
## Abstract ## BACKGROUND. Numerous studies have investigated the clinical significance of __BRAF__ mutation in papillary thyroid carcinoma (PTC). However, there have been conflicting data on the usefulness of __BRAF__ mutation as a prognostic marker of PTC. To address this controversy, the freque
## life* Peripheral blood B cells of a 67-year-old person were separated into IgM+IgD+, IgM+IgD-, and IgM-IgD-subsets, and nucleotide sequences of expressed immunoglobulin light chain variable (V) regions encoded by V,3 and V,4 gene family members were determined from amplified cDNA. V region sequ