Abstract

Chronic obstructive pulmonary disease (COPD) is a type of progressive lung disease, featured by airflow obstruction. Recently, a comprehensive analysis of the transcriptome in lung tissue of COPD patients was performed, but the heterogeneity of the sample was not seriously considered in characterizing the mechanistic dysregulation of COPD. Here, we established a new transcriptome analysis pipeline using a deconvolution process to reduce the heterogeneity and clearly identified that these transcriptome data originated from the mild or moderate stage of COPD patients. Differentially expressed or co-expressed genes in the protein interaction subnetworks were linked with mitochondrial dysfunction and the immune response, as expected. Computational protein localization prediction revealed that 19 proteins showing changes in subcellular localization were mostly related to mitochondria, suggesting that mislocalization of mitochondria-targeting proteins plays an important role in COPD pathology. Our extensive evaluation of COPD transcriptome data could provide guidelines for analyzing heterogeneous gene expression profiles and classifying potential candidate genes that are responsible for the pathogenesis of COPD.

Highlights

  • Chronic obstructive pulmonary disease (COPD), or chronic obstructive pulmonary disease, is a type of obstructive lung disease characterized by long-term poor airflow [1]

  • It is expected that diverse causes and symptoms of COPD may lead to heterogeneous gene expression profiles in individual COPD patients, as mentioned by Wedzicha [3]

  • These results revealed 8 heterogeneity in the COPD samples and indicated that simple conventional differentially expressed genes (DEGs) comparison was not enough to classify the samples

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Summary

Introduction

COPD, or chronic obstructive pulmonary disease, is a type of obstructive lung disease characterized by long-term poor airflow [1]. It is a general term referring to chronic bronchitis, emphysema, and refractory (non-reversible) asthma. These progressive lung diseases are commonly characterized by increased shortness of breath, frequent coughing, increased breathlessness, and wheezing. It is expected that diverse causes and symptoms of COPD may lead to heterogeneous gene expression profiles in individual COPD patients, as mentioned by Wedzicha [3]. More than 70% of COPD patients suffer from limited physical activity, and 50% among them can not lead a normal life [4,5]. In 2015, COPD ranked as the third leading cause of death worldwide, and it is expected that the mortality from COPD will increase greatly by 2030 [1]

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