Exploring Molecular Mechanisms and Biomarkers in COPD: An Overview of Current Advancements and Perspectives.
Chin-Ling LiShih-Feng LiuPublished in: International journal of molecular sciences (2024)
Chronic obstructive pulmonary disease (COPD) plays a significant role in global morbidity and mortality rates, typified by progressive airflow restriction and lingering respiratory symptoms. Recent explorations in molecular biology have illuminated the complex mechanisms underpinning COPD pathogenesis, providing critical insights into disease progression, exacerbations, and potential therapeutic interventions. This review delivers a thorough examination of the latest progress in molecular research related to COPD, involving fundamental molecular pathways, biomarkers, therapeutic targets, and cutting-edge technologies. Key areas of focus include the roles of inflammation, oxidative stress, and protease-antiprotease imbalances, alongside genetic and epigenetic factors contributing to COPD susceptibility and heterogeneity. Additionally, advancements in omics technologies-such as genomics, transcriptomics, proteomics, and metabolomics-offer new avenues for comprehensive molecular profiling, aiding in the discovery of novel biomarkers and therapeutic targets. Comprehending the molecular foundation of COPD carries substantial potential for the creation of tailored treatment strategies and the enhancement of patient outcomes. By integrating molecular insights into clinical practice, there is a promising pathway towards personalized medicine approaches that can improve the diagnosis, treatment, and overall management of COPD, ultimately reducing its global burden.
Keyphrases
- chronic obstructive pulmonary disease
- lung function
- oxidative stress
- single cell
- clinical practice
- mass spectrometry
- physical activity
- single molecule
- multiple sclerosis
- dna damage
- dna methylation
- ischemia reperfusion injury
- diabetic rats
- copy number
- induced apoptosis
- endoplasmic reticulum stress
- replacement therapy
- heat shock protein