Cancers, Vol. 11, Pages 1200: SRSF2 Mutations in Uveal Melanoma: A Preference for In-Frame Deletions?
Conclusions: Whereas in myelodysplastic syndrome predominantly missense SRSF2 mutations are described, the observed SRSF2 mutations in UM are all in-frame deletions of 8–9 amino acids. This suggests that the R625 missense SF3B1 mutations and SRSF2 mutations in UM are different compared to the spliceosome gene mutations in hematological cancers, and probably target a different, as yet unknown, set of genes involved in uveal melanoma etiology.
Source: Cancers - Category: Cancer & Oncology Authors: Natasha M. van Poppelen Wojtek Drabarek Kyra N. Smit Jolanda Vaarwater Tom Brands Dion Paridaens Emine Kili รง Annelies de Klein Tags: Communication Source Type: research
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