Cancers, Vol. 18, Pages 580: Novel Blood-Based Extracellular Vesicle-Derived Biomarkers in Small Cell Lung Cancer Identified via Proximity Extension Assay

Cancers doi: 10.3390/cancers18040580

Authors:
Hubert Krzyslak
Weronika Maria Szejniuk
Marwan Malluhi
Henrik Steglich-Arnholm
Ursula Falkmer
Jonas Ellegaard Mortensen
Søren Risom Kristensen
Shona Pedersen

Background: Small cell lung cancer (SCLC) is an aggressive malignancy with rapid progression and early metastasis, yet it lacks validated biomarkers for early diagnosis and treatment monitoring. Extracellular vesicles (EVs) are nano-sized particles released by cells that carry cargo reflective of their origin, making them promising candidates for liquid biopsy-based biomarker discovery. Methods: Plasma-derived EVs were isolated from 29 SCLC patients and 28 healthy controls (HCs) using ultracentrifugation and characterized via nanoparticle tracking analysis (NTA) and transmission electron microscopy (TEM). Proteomic profiling was performed using the Olink® Immuno-Oncology panel. Group differences were analyzed using multivariate models (Boruta, Elastic Net, and partial least squares discriminant analysis). Diagnostic potential was assessed using ROC analysis, and predictive response associations were evaluated by correlating EV protein changes with tumor size reduction (FDR-adjusted Spearman). Results: Of the 58 detected proteins, 36 were significantly upregulated in SCLC. PDGF-B, CXCL5, CCL17, EGF, and LAP-TGF-β1 showed good discriminatory performance (AUC 0.95–0.98). Additionally, a two-protein panel (LAP-TGF-β1 and PDGF-B) achieved an out-of-fold AUC of 0.96 (CI 0.89–1.00). NOS3, VEGFR-2, and ANGPT2 levels correlated inversely with tumor reduction after chemotherapy. Conclusions: These exploratory findings highlight EV proteomics as a minimally invasive platform for potential SCLC diagnosis and monitoring.

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Hubert Krzyslak www.mdpi.com