Proceedings of the fifth international RASopathies symposium: When development and cancer intersect
- PMID: 30302932
- PMCID: PMC6312476
- DOI: 10.1002/ajmg.a.40632
Proceedings of the fifth international RASopathies symposium: When development and cancer intersect
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.
Keywords: Costello syndrome; Legius syndrome; Noonan syndrome; RAS/MAPK; RASopathies; cardio-facio-cutaneous syndrome; clinical trial; neurofibromatosis type 1; signal transduction pathway; therapy.
© 2018 Wiley Periodicals, Inc.
References
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- Stephen AG, Esposito D, Bagni RK, & McCormick F (2014). Dragging Ras back in the ring. Cancer Cell, 25, 272–281. - PubMed
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- R01 CA131261/CA/NCI NIH HHS/United States
- International Costello Syndrome Support Group/International
- R01 CA176839/CA/NCI NIH HHS/United States
- R21 CA191392/CA/NCI NIH HHS/United States
- R35HL135742/NIH/NHLBI/International
- Onconova Therapeutics, Inc./International
- Pharmaceutical Research and Manufacturers of America (PhRMA)/International
- Prevention Genetics/International
- CFC International/International
- Costello Syndrome Family Network/International
- R01 AR062165/AR/NIAMS NIH HHS/United States
- P30 EY002162/EY/NEI NIH HHS/United States
- 5R35CA197709/NIH/NCI Outstanding Investigator Award/International
- Department of Genetics/International
- Onconova Therapeutics Inc/International
- Noonan Syndrome Foundation/International
- U01 CA202241/CA/NCI NIH HHS/United States
- PreventionGenetics/International
- Children's Tumor Foundation/International
- R35 CA197709/CA/NCI NIH HHS/United States
- GeneDx/International
- R13 CA217038/CA/NCI NIH HHS/United States
- R35 HL135742/HL/NHLBI NIH HHS/United States
- EveryLife Foundation for Rare Diseases/International
- School of Medicine/International
- University of Alabama at Birmingham/International
- 4-FY17-900/March of Dimes Foundation/International
- We Work for Health/International
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