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Recent Advances in Molecular Basis of Lung Aging and Its Associated Diseases. | LitMetric

Recent Advances in Molecular Basis of Lung Aging and Its Associated Diseases.

Tuberc Respir Dis (Seoul)

Section of Pulmonary, Critical Care and Sleep Medicine, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT, USA.

Published: April 2020

AI Article Synopsis

  • Aging is generally seen as a decline in fitness due to harmful changes in biological functions over time.
  • Recent research has shown that key molecular aspects of aging are linked to chronic lung diseases, such as COPD and idiopathic pulmonary fibrosis, which are notably influenced by advanced age.
  • This review aims to connect the molecular biology of aging with lung medicine, summarizing recent findings on age-related lung disorders to potentially inform new treatments.

Article Abstract

Aging is often viewed as a progressive decline in fitness due to cumulative deleterious alterations of biological functions in the living system. Recently, our understanding of the molecular mechanisms underlying aging biology has significantly advanced. Interestingly, many of the pivotal molecular features of aging biology are also found to contribute to the pathogenesis of chronic lung disorders such as chronic obstructive pulmonary disease and idiopathic pulmonary fibrosis, for which advanced age is the most crucial risk factor. Thus, an enhanced understanding of how molecular features of aging biology are intertwined with the pathobiology of these aging-related lung disorders has paramount significance and may provide an opportunity for the development of novel therapeutics for these major unmet medical needs. To serve the purpose of integrating molecular understanding of aging biology with pulmonary medicine, in this review, recent findings obtained from the studies of aging-associated lung disorders are summarized and interpreted through the perspective of molecular biology of aging.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7105435PMC
http://dx.doi.org/10.4046/trd.2020.0003DOI Listing

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