Author(s): Caldeira, Inês ; Silva, Hugo Miguel Fernandes ; Costa, Daniela Machado ; Correia-Pinto, Jorge ; Moura, Rute S.
Date: 2021
Persistent ID: https://hdl.handle.net/1822/76476
Origin: RepositóriUM - Universidade do Minho
Subject(s): Congenital pulmonary airway malformation (CPAM); Bronchopulmonary sequestration; Bronchogenic cysts; Congenital diaphragmatic hernia (CDH); Congenital malformations
Lung organogenesis is a highly coordinated process governed by a network of conserved signaling pathways that ultimately control patterning, growth, and differentiation. This rigorously regulated developmental process culminates with the formation of a fully functional organ. Conversely, failure to correctly regulate this intricate series of events results in severe abnormalities that may compromise postnatal survival or affect/disrupt lung function through early life and adulthood. Conditions like congenital pulmonary airway malformation, bronchopulmonary sequestration, bronchogenic cysts, and congenital diaphragmatic hernia display unique forms of lung abnormalities. The etiology of these disorders is not yet completely understood; however, specific developmental pathways have already been reported as deregulated. In this sense, this review focuses on the molecular mechanisms that contribute to normal/abnormal lung growth and development and their impact on postnatal survival.
