| Literature DB >> 29397482 |
Eugenia Manevitz-Mendelson1, Gil S Leichner1, Ortal Barel2, Inbal Davidi-Avrahami3, Limor Ziv-Strasser2, Eran Eyal2, Itai Pessach4,5, Uri Rimon6, Aviv Barzilai1,4, Abraham Hirshberg7, Keren Chechekes2, Ninette Amariglio4,2, Gideon Rechavi4,2, Karina Yaniv3, Shoshana Greenberger8,9.
Abstract
Generalized lymphatic anomaly (GLA or lymphangiomatosis) is a rare disease characterized by a diffuse proliferation of lymphatic vessels in skin and internal organs. It often leads to progressive respiratory failure and death, but its etiology is unknown. Here, we isolated lymphangiomatosis endothelial cells from GLA tissue. These cells were characterized by high proliferation and survival rates, but displayed impaired capacities for migration and tube formation. We employed whole exome sequencing to search for disease-causing genes and identified a somatic mutation in NRAS. We used mouse and zebrafish model systems to initially evaluate the role of this mutation in the development of the lymphatic system, and we studied the effect of drugs blocking the downstream effectors, mTOR and ERK, on this disease.Entities:
Keywords: Lymphangiomatosis; Mutation; NRAS
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Year: 2018 PMID: 29397482 DOI: 10.1007/s10456-018-9595-8
Source DB: PubMed Journal: Angiogenesis ISSN: 0969-6970 Impact factor: 9.596