| Literature DB >> 25959926 |
Nataliia V Guz1, Maxim E Dokukin2, Craig D Woodworth3, Andrew Cardin1, Igor Sokolov4.
Abstract
We used AFM HarmoniX modality to analyse the surface of individual human cervical epithelial cells at three stages of progression to cancer, normal, immortal (pre-malignant) and carcinoma cells. Primary cells from 6 normal strains, 6 cancer, and 6 immortalized lines (derived by plasmid DNA-HPV-16 transfection of cells from 6 healthy individuals) were tested. This cell model allowed for good control of the cell phenotype down to the single cell level, which is impractical to attain in clinical screening tests (ex-vivo). AFM maps of physical (nonspecific) adhesion are collected on fixed dried cells. We show that a surface parameter called fractal dimension can be used to segregate normal from both immortal pre-malignant and malignant cells with sensitivity and specificity of more than 99%. The reported method of analysis can be directly applied to cells collected in liquid cytology screening tests and identified as abnormal with regular optical methods to increase sensitivity. FROM THE CLINICAL EDITOR: Despite cervical smear screening, sometimes it is very difficult to differentiate cancers cells from pre-malignant cells. By using AFM to analyze the surface properties of human cervical epithelial cells, the authors were able to accurately identify normal from abnormal cells. This method could augment existing protocols to increase diagnostic accuracy.Entities:
Keywords: Atomic force microscopy; Cervical cancer; Early cancer detection; Novel detection methods; Pap smear/liquid cytology tests
Mesh:
Year: 2015 PMID: 25959926 PMCID: PMC5518320 DOI: 10.1016/j.nano.2015.04.012
Source DB: PubMed Journal: Nanomedicine ISSN: 1549-9634 Impact factor: 5.307