# Whispers in the Lungs: Small Extracellular Vesicles in Lung Cancer and COPD Crosstalk

**Authors:** Yetemwork Aleka, Fantahun Biadglegne, Ulrich Sack

PMC · DOI: 10.3390/cancers17101612 · Cancers · 2025-05-09

## TL;DR

This paper reviews how tiny cell particles called sEVs could help diagnose and monitor lung cancer and COPD, but more research is needed to make them clinically useful.

## Contribution

Highlights the dual role of sEVs in lung cancer and COPD as potential biomarkers and emphasizes the need for large-scale studies.

## Key findings

- sEVs from lung cancer carry onco-proteins like EGFR mutations and miR-21.
- sEVs from COPD contain pro-inflammatory cytokines like IL-6 and TNF-α.
- sEVs show promise as biomarkers but face challenges in clinical application due to extraction and analysis limitations.

## Abstract

Lung cancer is a very serious disease, and it becomes worse when combined with chronic obstructive pulmonary disease [COPD], another chronic lung illness. Both are linked to smoking and long-term lung inflammation. Scientists are now focusing on tiny particles called small extracellular vesicles (sEVs), which are released by cells and carry important molecules. In lung cancer, sEVs often carry cancer-related signals, while in COPD, they carry inflammation-related ones. These signals could help doctors to diagnose and monitor the diseases more accurately. However, collecting and studying sEVs is still difficult, which limits their use in clinics. This review looks at the potential of sEVs as helpful tools in treating lung cancer and COPD and highlights the need for more research.

Lung cancer is one of the deadliest forms of cancer. Its prognosis becomes even worse when it co-occurs with other diseases, such as chronic obstructive pulmonary disease (COPD). Both illnesses have numerous shared risk factors, including the use of tobacco smoke, and have similar underlying mechanisms like long-term inflammation. There are some other less studied but equally important molecules, like small extracellular vesicles (sEVs), that have been shown to mediate effective communication at the cellular level and may affect the progression of a disease or cause resistance to therapies. In sEVs from lung cancer tumors, there are onco-proteins (e.g., tumor initiator EGFR mutations, onco-miR, miR-21), while in sEVs from patients with COPD, there are pro-inflammatory cytokines like IL-6 and TNF-α that enhance airway inflammation. These potential biomarkers of sEVs from chronic lung disease have great value in defense against emerging health problems; however, limitations in sample extraction and analysis are obstacles that hinder clinical enhanced applicability. This review focuses on sEV-derived biomarkers in lung cancer and COPD for diagnostic, prognostic, and therapeutic monitoring purposes. To make these molecules more useful in real-life therapy and determine their signature’s role, further investigation with a high-scale study is necessary.

## Linked entities

- **Genes:** EGFR (epidermal growth factor receptor) [NCBI Gene 1956]
- **Proteins:** IL6 (interleukin 6), TNF (tumor necrosis factor)
- **Diseases:** lung cancer (MONDO:0005138), chronic obstructive pulmonary disease (MONDO:0005002), COPD (MONDO:0005002)

## Full-text entities

- **Genes:** TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, MIR21 (microRNA 21) [NCBI Gene 406991] {aka MIRN21, hsa-mir-21, miR-21, miRNA21}, EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}
- **Diseases:** COPD (MESH:D029424), Lung Cancer (MESH:D008175), cancer (MESH:D009369), airway inflammation (MESH:D007249), lung disease (MESH:D008171), long-term inflammation (MESH:D000088562)
- **Species:** Homo sapiens (human, species) [taxon 9606], Nicotiana tabacum (American tobacco, species) [taxon 4097]

## Full text

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## Figures

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## References

91 references — full list in the complete paper: https://tomesphere.com/paper/PMC12110411/full.md

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Source: https://tomesphere.com/paper/PMC12110411