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Etiology and Genetics of Congenital Vascular Lesions.
Queisser, Angela; Boon, Laurence M; Vikkula, Miikka.
Afiliação
  • Queisser A; Human Molecular Genetics, de Duve Institute, University of Louvain, Avenue Hippocrate 74 (+5), Brussels B-1200, Belgium.
  • Boon LM; Human Molecular Genetics, de Duve Institute, University of Louvain, Avenue Hippocrate 74 (+5), Brussels B-1200, Belgium; Division of Plastic Surgery, Center for Vascular Anomalies, Cliniques Universitaires St Luc, Avenue Hippocrate 10, B-1200 Brussels, Belgium.
  • Vikkula M; Human Molecular Genetics, de Duve Institute, University of Louvain, Avenue Hippocrate 74 (+5), Brussels B-1200, Belgium. Electronic address: miikka.vikkula@uclouvain.be.
Otolaryngol Clin North Am ; 51(1): 41-53, 2018 Feb.
Article em En | MEDLINE | ID: mdl-29217067
ABSTRACT
The detection of somatic, activating genetic mutations to underlie development of vascular tumors and malformations led to a better understanding of their pathophysiology. Proteins encoded by the detected mutated genes activate the two major signaling pathways, also involved in cancer the RAS/MAPK/ERK pathway and/or the PI3K/AKT/mTOR pathway. This gives a strong basis for studies to repurpose cancer therapeutics to patients with vascular tumors and malformations.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Malformações Arteriovenosas / Transdução de Sinais / Anormalidades Linfáticas / Neoplasias de Cabeça e Pescoço / Hemangioma Tipo de estudo: Etiology_studies Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Malformações Arteriovenosas / Transdução de Sinais / Anormalidades Linfáticas / Neoplasias de Cabeça e Pescoço / Hemangioma Tipo de estudo: Etiology_studies Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article