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Proceedings of the fifth international RASopathies symposium: When development and cancer intersect.

Authors :
Rauen KA
Schoyer L
Schill L
Stronach B
Albeck J
Andresen BS
Cavé H
Ellis M
Fruchtman SM
Gelb BD
Gibson CC
Gripp K
Hefner E
Huang WYC
Itkin M
Kerr B
Linardic CM
McMahon M
Oberlander B
Perlstein E
Ratner N
Rogers L
Schenck A
Shankar S
Shvartsman S
Stevenson DA
Stites EC
Stork PJS
Sun C
Therrien M
Ullian EM
Widemann BC
Yeh E
Zampino G
Zenker M
Timmer W
McCormick F
Source :
American journal of medical genetics. Part A [Am J Med Genet A] 2018 Dec; Vol. 176 (12), pp. 2924-2929. Date of Electronic Publication: 2018 Oct 10.
Publication Year :
2018

Abstract

This report summarizes and highlights the fifth International RASopathies Symposium: When Development and Cancer Intersect, held in Orlando, Florida in July 2017. The RASopathies comprise a recognizable pattern of malformation syndromes that are caused by germ line mutations in genes that encode components of the RAS/mitogen-activated protein kinase (MAPK) pathway. Because of their common underlying pathogenetic etiology, there is significant overlap in their phenotypic features, which includes craniofacial dysmorphology, cardiac, cutaneous, musculoskeletal, gastrointestinal and ocular abnormalities, neurological and neurocognitive issues, and a predisposition to cancer. The RAS pathway is a well-known oncogenic pathway that is commonly found to be activated in somatic malignancies. As in somatic cancers, the RASopathies can be caused by various pathogenetic mechanisms that ultimately impact or alter the normal function and regulation of the MAPK pathway. As such, the RASopathies represent an excellent model of study to explore the intersection of the effects of dysregulation and its consequence in both development and oncogenesis.<br /> (© 2018 Wiley Periodicals, Inc.)

Details

Language :
English
ISSN :
1552-4833
Volume :
176
Issue :
12
Database :
MEDLINE
Journal :
American journal of medical genetics. Part A
Publication Type :
Report
Accession number :
30302932
Full Text :
https://doi.org/10.1002/ajmg.a.40632