Pulmonary Fibrosis and Lung Cancer: Pathophysiology and Novel Therapeutic Approaches

A special issue of Journal of Respiration (ISSN 2673-527X).

Deadline for manuscript submissions: 20 June 2025 | Viewed by 2670

Special Issue Editor


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Guest Editor
Pauley Heart Center, Department of Internal Medicine, Cardiology Division, Virginia Commonwealth University, Richmond, VA, USA
Interests: cellular signaling; myocardial infarction; ischemia reperfusion injury; heart failure; epigenetics; non-coding RNA; microRNA; pulmonary hypertension; lung fibrosis; vascular remodeling; phosphodiesterase; mTOR signaling
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Special Issue Information

Dear Colleagues,

Pulmonary fibrosis (PF) is a progressive chronic interstitial lung disease characterized by robust remodeling and scarring of the lung that results in stiffening of the lung vasculature and causes other pathological changes that compromise the lung function. PF is caused by several factors, including inflammation, smoking and genetic mutation. PF also manifests as secondary to other lung diseases, including pulmonary hypertension, and is caused due to other unknown etiologies that are collectively defined as idiopathic pulmonary fibrosis (IPF), a major type of PF. Despite ongoing efforts to identify a cure, currently, there is no medication for PF, and treatment options largely rely on impeding lung scarring with drugs and steroids, with lung transplantation being the last resort in severe cases of PF (with limited success). Moreover, patients diagnosed with IPF have a significantly increased risk of developing lung cancer, which further complicates the prognosis and treatment modalities of IPF. The global incidence of PF and lung cancer increases every year, with a higher rate of morbidity and mortality being seen worldwide. Therefore, there is an urgent need to understand the pathophysiology and molecular mechanisms underlying the complex disease of PF and lung cancer and to identify novel and effective treatment strategies to improve the quality of life of PF and the lung cancer patient community.

This Special Issue aims to provide our readers with current knowledge and understandings regarding novel therapeutic approaches for the treatment of PF and lung cancer. We welcome original research articles, reviews, meta-analyses/systematic reviews, or shorter perspective articles, as well novel technological approaches on all aspects related to the pathophysiological and molecular aspects and treatment options of pulmonary fibrosis, whether it be caused by inflammation, genetic aberration, lung cancer, and other idiopathic etiologies, including pulmonary hypertension.

Dr. Arun Samidurai
Guest Editor

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Keywords

  • pulmonary fibrosis
  • pulmonary arterial hypertension
  • myocardial infarction
  • epigenetics

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Published Papers (1 paper)

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Research

14 pages, 313 KiB  
Article
Clinical and Functional Characteristics of Interstitial Lung Disease in Algeria: A Single-Center Prospective Study
by Abdelbassat Ketfi, Fayçal Selatni, Cherifa Djouadi and Rama Touahri
J. Respir. 2024, 4(1), 12-25; https://doi.org/10.3390/jor4010002 - 29 Dec 2023
Viewed by 1737
Abstract
Introduction: There are a limited number of epidemiological studies describing the global burden of chronic diffuse interstitial lung diseases (ILD) and their subtypes’ heterogeneity worldwide. Our main is to characterize new-onset ILDs in Algeria and compare our results with data from other populations. [...] Read more.
Introduction: There are a limited number of epidemiological studies describing the global burden of chronic diffuse interstitial lung diseases (ILD) and their subtypes’ heterogeneity worldwide. Our main is to characterize new-onset ILDs in Algeria and compare our results with data from other populations. Materials and Methods: Newly diagnosed ILDs were prospectively collected in a single-center observational cohort study including all patients diagnosed as ILDs in the pulmonology, phthisiology, and allergology departments between 2015 and 2019. Detailed anamnestic and clinical data were collected at the time of diagnosis. The results of high-resolution computed tomography (HRCT), serological tests, biology data, and respiratory functional exploration were systematically performed and collected. Results: A total of 455 cases were included. The mean age was 59.4 ± 13.2 years. There was a slight predominance of females (300; 65.9%). The most common disease was ILD secondary to connective tissue disease (CTD) or ILD-CTD (48.1%), followed by idiopathic interstitial pneumonias (IIPs) (23.5%), sarcoidosis (16.9%), interstitial pneumonia with autoimmune features (IPAF) (12.1%), and hypersensitivity pneumonitis (HP) (2.4%). Idiopathic pulmonary fibrosis (IPF) was present in 8.6% and unclassifiable ILD in 4.6% of the total ILD cases. Conclusions: ILD-CTD, IIP, and sarcoidosis were the most frequently observed ILDs in this Algerian population. Similarities and many differences were found compared to previous data from other countries. Full article
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