MicroRNA Monitoring in Human Alveolar Macrophages from Patients with Smoking-Related Lung Diseases: A Preliminary Study

Author:

Mirra Davida1,Esposito Renata1ORCID,Spaziano Giuseppe1ORCID,Sportiello Liberata23,Panico Francesca4,Squillante Antonio5,Falciani Maddalena6,Cerqua Ida7ORCID,Gallelli Luca4ORCID,Cione Erika8ORCID,D’Agostino Bruno1

Affiliation:

1. Department of Environmental Biological and Pharmaceutical Sciences and Technologies, University of Campania “Luigi Vanvitelli”, 81100 Caserta, Italy

2. Campania Regional Centre for Pharmacovigilance and Pharmacoepidemiology, 80138 Naples, Italy

3. Department of Experimental Medicine-Section of Pharmacology “L. Donatelli”, University of Campania “Luigi Vanvitelli”, 80138 Naples, Italy

4. Department of Health Sciences, University of “Magna Graecia”, 88100 Catanzaro, Italy

5. Department of Medicine, University of Salerno, 84100 Salerno, Italy

6. Pulmonary and Critical Care Medicine, Ospedale Scarlato, 84018 Scafati, Italy

7. Department of Pharmacy, University Federico II of Naples, Via D. Montesano 49, 80131 Naples, Italy

8. Department of Pharmacy, Health and Nutritional Sciences, University of Calabria, 87036 Rende, Italy

Abstract

Chronic obstructive pulmonary disease (COPD) is a progressive lung disease that is commonly considered to be a potent driver of non-small cell lung cancer (NSCLC) development and related mortality. A growing body of evidence supports a role of the immune system, mainly played by alveolar macrophages (AMs), in key axes regulating the development of COPD or NSCLC phenotypes in response to harmful agents. MicroRNAs (miRNAs) are small non-coding RNAs that influence most biological processes and interfere with several regulatory pathways. The purpose of this study was to assess miRNA expression patterns in patients with COPD, NSCLC, and ever- or never-smoker controls to explore their involvement in smoking-related diseases. Bronchoalveolar lavage (BAL) specimens were collected from a prospective cohort of 43 sex-matched subjects to determine the expressions of hsa-miR-223-5p, 16-5p, 20a-5p, -17-5p, 34a-5p and 106a-5p by RT-PCR. In addition, a bioinformatic analysis of miRNA target genes linked to cancer was performed. Distinct and common miRNA expression levels were identified in each pathological group, suggesting their possible role as an index of NSCLC or COPD microenvironment. Moreover, we identified miRNA targets linked to carcinogenesis using in silico analysis. In conclusion, this study identified miRNA signatures in AMs, allowing us to understand the molecular mechanisms underlying smoking-related conditions and potentially providing new insights for diagnosis or pharmacological treatment.

Publisher

MDPI AG

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