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The seventh international RASopathies symposium: Pathways to a cure-expanding knowledge, enhancing research, and therapeutic discovery.

Kontaridis, MI; Roberts, AE; Schill, L; Schoyer, L; Stronach, B; Andelfinger, G; Aoki, Y; Axelrad, ME; Bakker, A; Bennett, AM; et al. Kontaridis, MI; Roberts, AE; Schill, L; Schoyer, L; Stronach, B; Andelfinger, G; Aoki, Y; Axelrad, ME; Bakker, A; Bennett, AM; Broniscer, A; Castel, P; Chang, CA; Cyganek, L; Das, TK; den Hertog, J; Galperin, E; Garg, S; Gelb, BD; Gordon, K; Green, T; Gripp, KW; Itkin, M; Kiuru, M; Korf, BR; Livingstone, JR; López-Juárez, A; Magoulas, PL; Mansour, S; Milner, T; Parker, E; Pierpont, EI; Plouffe, K; Rauen, KA; Shankar, SP; Smith, SB; Stevenson, DA; Tartaglia, M; Van, R; Wagner, ME; Ware, SM; Zenker, M (2022) The seventh international RASopathies symposium: Pathways to a cure-expanding knowledge, enhancing research, and therapeutic discovery. Am J Med Genet A, 188 (6). pp. 1915-1927. ISSN 1552-4833 https://doi.org/10.1002/ajmg.a.62716
SGUL Authors: Mansour, Sahar

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Abstract

RASopathies are a group of genetic disorders that are caused by genes that affect the canonical Ras/mitogen-activated protein kinase (MAPK) signaling pathway. Despite tremendous progress in understanding the molecular consequences of these genetic anomalies, little movement has been made in translating these findings to the clinic. This year, the seventh International RASopathies Symposium focused on expanding the research knowledge that we have gained over the years to enhance new discoveries in the field, ones that we hope can lead to effective therapeutic treatments. Indeed, for the first time, research efforts are finally being translated to the clinic, with compassionate use of Ras/MAPK pathway inhibitors for the treatment of RASopathies. This biannual meeting, organized by the RASopathies Network, brought together basic scientists, clinicians, clinician scientists, patients, advocates, and their families, as well as representatives from pharmaceutical companies and the National Institutes of Health. A history of RASopathy gene discovery, identification of new disease genes, and the latest research, both at the bench and in the clinic, were discussed.

Item Type: Article
Additional Information: © 2022 The Authors. American Journal of Medical Genetics Part A published by Wiley Periodicals LLC. This is an open access article under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
Keywords: Costello syndrome, Noonan syndrome, RASopathy, cardiofaciocutaneus syndrome, neurofibromatosis, signaling, cardiofaciocutaneus syndrome, Costello syndrome, neurofibromatosis, Noonan syndrome, RASopathy, signaling, 1103 Clinical Sciences, 0604 Genetics
SGUL Research Institute / Research Centre: Academic Structure > Molecular and Clinical Sciences Research Institute (MCS)
Journal or Publication Title: Am J Med Genet A
ISSN: 1552-4833
Language: eng
Dates:
DateEvent
16 May 2022Published
9 March 2022Published Online
5 February 2022Accepted
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
UNSPECIFIEDCFC InternationalUNSPECIFIED
UNSPECIFIEDChildren's Tumor Foundationhttp://dx.doi.org/10.13039/100001545
UNSPECIFIEDCostello Syndrome Family NetworkUNSPECIFIED
UNSPECIFIEDInternational Costello Syndrome Support GroupUNSPECIFIED
UNSPECIFIEDNational Center For Advancing Translational Sciences and the National Institute for Child Health and Human Development of the National Institutes of HealthUNSPECIFIED
UNSPECIFIEDNeurofibromatosis NetworkUNSPECIFIED
UNSPECIFIEDNIH-R01-HL102368UNSPECIFIED
UNSPECIFIEDNIH-R35 HL125742UNSPECIFIED
UNSPECIFIEDNoonan Syndrome AssociationUNSPECIFIED
UNSPECIFIEDNoonan Syndrome FoundationUNSPECIFIED
UNSPECIFIEDNoonan UKUNSPECIFIED
UNSPECIFIEDMasonic Medical Research InstituteUNSPECIFIED
UNSPECIFIEDRevolution MedicinesUNSPECIFIED
UNSPECIFIEDOnconova TherapeuticsUNSPECIFIED
UNSPECIFIEDDay One BiopharmaceuticalsUNSPECIFIED
UNSPECIFIEDBoehringer Ingelheim Fondshttp://dx.doi.org/10.13039/501100001645
UNSPECIFIEDIgia PharmaceuticalsUNSPECIFIED
R13TR003727Human Development of the National Institutes of HealthUNSPECIFIED
UNSPECIFIEDNational Institute for Child HealthUNSPECIFIED
UNSPECIFIEDNational Center for Advancing Translational Scienceshttp://dx.doi.org/10.13039/100006108
NIH-R35 HL125742National Institutes of Healthhttp://dx.doi.org/10.13039/100000002
NIH-R01-HL102368National Institutes of Healthhttp://dx.doi.org/10.13039/100000002
PubMed ID: 35266292
Web of Science ID: WOS:000766395600001
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/114220
Publisher's version: https://doi.org/10.1002/ajmg.a.62716

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