TIE1 as a Candidate Gene for Lymphatic Malformations with or without Lymphedema

Author:

Michelini SandroORCID,Ricci Maurizio,Veselenyiova DominikaORCID,Kenanoglu SercanORCID,Kurti Danjela,Baglivo Mirko,Fiorentino Alessandro,Basha Syed HussainORCID,Priya Sasi,Serrani Roberta,Krajcovic Juraj,Dundar MunisORCID,Dautaj AstritORCID,Bertelli MatteoORCID

Abstract

TIE1 is a cell surface protein expressed in endothelial cells. Involved in angiogenesis and lymphangiogenesis, including morphogenesis of lymphatic valves, TIE1 is important for lymphatic system functional integrity. The main purpose of this study was to identify different variants in the TIE1 gene that could be associated with lymphatic malformations or dysfunction and predisposition for lymphedema. In a cohort of 235 Italian lymphedema patients, who tested negative for variants in known lymphedema genes, we performed a further test for new candidate genes, including TIE1. Three probands carried different variants in TIE1. Two of these segregated with lymphedema or lymphatic dysfunction in familial cases. Variants in TIE1 could contribute to the onset of lymphedema. On the basis of our findings, we propose TIE1 as a candidate gene for comprehensive genetic testing of lymphedema.

Funder

Provincia Autonoma di Trento

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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