Literature DB >> 29722020

Atrioventricular canal defect and genetic syndromes: The unifying role of sonic hedgehog.

M C Digilio1, F Pugnaloni2, A De Luca3, G Calcagni1, A Baban1, M L Dentici1, P Versacci2, B Dallapiccola1, M Tartaglia1, B Marino2.   

Abstract

The atrioventricular canal defect (AVCD) is a congenital heart defect (CHD) frequently associated with extracardiac anomalies (75%). Previous observations from a personal series of patients with AVCD and "polydactyly syndromes" showed that the distinct morphology and combination of AVCD features in some of these syndromes is reminiscent of the cardiac phenotype found in heterotaxy, a malformation complex previously associated with functional cilia abnormalities and aberrant Hedgehog (Hh) signaling. Hh signaling coordinates multiple aspects of left-right lateralization and cardiovascular growth. Being active at the venous pole the secondary heart field (SHF) is essential for normal development of dorsal mesenchymal protrusion and AVCD formation and septation. Experimental data show that perturbations of different components of the Hh pathway can lead to developmental errors presenting with partially overlapping manifestations and AVCD as a common denominator. We review the potential role of Hh signaling in the pathogenesis of AVCD in different genetic disorders. AVCD can be viewed as part of a "developmental field," according to the concept that malformations can be due to defects in signal transduction cascades or pathways, as morphogenetic units which may be altered by Mendelian mutations, aneuploidies, and environmental causes.
© 2018 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  atrioventricular septal defect; cilium; heterotaxy; secondary heart field; sonic hedgehog; syndrome

Mesh:

Substances:

Year:  2018        PMID: 29722020     DOI: 10.1111/cge.13375

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  7 in total

1.  A PKA inhibitor motif within SMOOTHENED controls Hedgehog signal transduction.

Authors:  John T Happ; Corvin D Arveseth; Jessica Bruystens; Daniela Bertinetti; Isaac B Nelson; Cristina Olivieri; Jingyi Zhang; Danielle S Hedeen; Ju-Fen Zhu; Jacob L Capener; Jan W Bröckel; Lily Vu; C C King; Victor L Ruiz-Perez; Xuecai Ge; Gianluigi Veglia; Friedrich W Herberg; Susan S Taylor; Benjamin R Myers
Journal:  Nat Struct Mol Biol       Date:  2022-10-06       Impact factor: 18.361

Review 2.  A change of heart: new roles for cilia in cardiac development and disease.

Authors:  Lydia Djenoune; Kathryn Berg; Martina Brueckner; Shiaulou Yuan
Journal:  Nat Rev Cardiol       Date:  2021-12-03       Impact factor: 49.421

3.  Germline and Mosaic Variants in PRKACA and PRKACB Cause a Multiple Congenital Malformation Syndrome.

Authors:  Adrian Palencia-Campos; Phillip C Aoto; Erik M F Machal; Ana Rivera-Barahona; Patricia Soto-Bielicka; Daniela Bertinetti; Blaine Baker; Lily Vu; Francesca Piceci-Sparascio; Isabella Torrente; Eveline Boudin; Silke Peeters; Wim Van Hul; Celine Huber; Dominique Bonneau; Michael S Hildebrand; Matthew Coleman; Melanie Bahlo; Mark F Bennett; Amy L Schneider; Ingrid E Scheffer; Maria Kibæk; Britta S Kristiansen; Mahmoud Y Issa; Mennat I Mehrez; Samira Ismail; Jair Tenorio; Gaoyang Li; Bjørn Steen Skålhegg; Ghada A Otaify; Samia Temtamy; Mona Aglan; Aia E Jønch; Alessandro De Luca; Geert Mortier; Valérie Cormier-Daire; Alban Ziegler; Mathew Wallis; Pablo Lapunzina; Friedrich W Herberg; Susan S Taylor; Victor L Ruiz-Perez
Journal:  Am J Hum Genet       Date:  2020-10-14       Impact factor: 11.025

4.  Model system identification of novel congenital heart disease gene candidates: focus on RPL13.

Authors:  Analyne M Schroeder; Massoud Allahyari; Georg Vogler; Maria A Missinato; Tanja Nielsen; Michael S Yu; Jeanne L Theis; Lars A Larsen; Preeya Goyal; Jill A Rosenfeld; Timothy J Nelson; Timothy M Olson; Alexandre R Colas; Paul Grossfeld; Rolf Bodmer
Journal:  Hum Mol Genet       Date:  2019-12-01       Impact factor: 6.150

Review 5.  Genetics of atrioventricular canal defects.

Authors:  Flaminia Pugnaloni; Maria Cristina Digilio; Carolina Putotto; Enrica De Luca; Bruno Marino; Paolo Versacci
Journal:  Ital J Pediatr       Date:  2020-05-13       Impact factor: 2.638

6.  Deleterious Rare Mutations of GLI1 Dysregulate Sonic Hedgehog Signaling in Human Congenital Heart Disease.

Authors:  Rui Peng; Binbin Li; Shuxia Chen; Zhiwen Shi; Liwei Yu; Yunqian Gao; Xueyan Yang; Lei Lu; Hongyan Wang
Journal:  Front Cardiovasc Med       Date:  2022-04-04

Review 7.  Cardiac Defects and Genetic Syndromes: Old Uncertainties and New Insights.

Authors:  Giulio Calcagni; Flaminia Pugnaloni; Maria Cristina Digilio; Marta Unolt; Carolina Putotto; Marcello Niceta; Anwar Baban; Francesca Piceci Sparascio; Fabrizio Drago; Alessandro De Luca; Marco Tartaglia; Bruno Marino; Paolo Versacci
Journal:  Genes (Basel)       Date:  2021-07-08       Impact factor: 4.096

  7 in total

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