Powering single-cell genomics to unravel circulating tumour cell subpopulations in non-small cell lung cancer patients.

Background: Circulating tumour cells (CTCs) are attractive "liquid biopsy" candidates that could provide insights into the different phenotypes of tumours present within a patient. The epithelial-to-mesenchymal transition (EMT) of CTCs is considered a critical step in tumour metastasis; however, it may confound traditional epithelial feature-based CTC isolation and detection. We applied single-cell copy number alteration (CNA) analysis for the identification of genomic alterations to confirm the neoplastic nature of circulating cells with only mesenchymal phenotypes.

Methods: We isolated CTCs from blood samples collected from 46 NSCLC patients using the Parsortix system. Enriched cells were subjected to immunofluorescent staining for CTC identification using a multi-marker panel comprising both epithelial and mesenchymal markers. A subset of isolated CTCs was subjected to whole genome amplification (WGA) and low-pass whole-genome sequencing (LP-WGS) for the analysis of copy number alterations (CNAs).

Results: CTCs were detected in 16/46 (34.8%) patients, inclusive of CK/EpCAM CTCs (3/46, 6.5%) and Vim CTCs (13/46, 28.3%). Clusters of Vim cells were detected in 8 samples, which constitutes 50% of the total number of NSCLC patients with CTCs. No patients had detectable hybrid CK/EpCAM/Vim cells. All of the tested CK/EpCAM CTCs and 7/8 Vim CTCs or CTC clusters carried CNAs confirming their neoplastic nature. Notably, the Vim cluster with no CNAs was characterised by spindle morphology and, therefore, defined as normal mesenchymal circulating cells.

Conclusion: Our results revealed that CK-negative, vimentin-expressing cells represent a large proportion of CTCs detected in NSCLC patients, which are likely missed by standard epithelial-marker-dependent CTC categorisation.