Abstract

Inflammation, characterized by high numbers of infiltrating leukocytes and a high HLA Class I expression, is associated with a bad prognosis in uveal melanoma (UM). We wondered whether mutations in GNA11 or GNAQ differentially affect inflammation and HLA expression, and thereby progression of the disease. We analyzed data of 59 primarily enucleated UM eyes. The type of GNAQ/11 mutation was analyzed using dPCR; chromosome aberrations were determined by Fluorescence in Situ Hybridization (FISH), karyotyping, and single nucleotide polymorphism (SNP) analysis, and mRNA expression by Illumina PCR. Comparing tumors with a GNAQ mutation with those with a GNA11 mutation yielded no significant differences in histopathological characteristics, infiltrate, or HLA expression. When comparing the Q209L mutations with Q209P mutations in tumors with monosomy of chromosome 3, a higher mitotic count was found in the Q209P/M3 tumors (p = 0.007). The Kaplan-Meier (KM) curves between the patients of the different groups were not significantly different. We conclude that the type (Q209P/Q209L) or location of the mutation (GNA11/GNAQ) do not have a significant effect on the immunological characteristics of the tumors, such as infiltrate and HLA Class I expression. Chromosome 3 status was the main determinant in explaining the difference in infiltrate and HLA expression.

Highlights

  • Uveal melanoma (UM) is a form of cancer that occurs mostly in people aged 60 years and older and has a prevalence of around 5.0 per million people within The Netherlands [1]

  • There is no evidence that the differences in inflammation found in groups with the same chromosome 3 status are caused by the different mutations on GNAQ or GNA11 or the type of mutation

  • 3 status, we considered the option that the two types of mutations might differentially affect this inflammation

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Summary

Introduction

Uveal melanoma (UM) is a form of cancer that occurs mostly in people aged 60 years and older and has a prevalence of around 5.0 per million people within The Netherlands [1]. UM forms in the uvea, which is made up of the iris, the ciliary body, and the choroid. The primary GNAQ/GNA11 mutation in UM occurs in the melanocyte and is already present in choroidal nevi [3,4,5]. During malignant progression, this genetic modification is usually followed by gain of chromosome 6q or gain of 8q, as well as a mutation in the BAP1, EIF1AX, or SF3B1 gene [6,7,8], and/or a complete loss of one chromosome 3 (monosomy 3 (M3)).

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