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A multivariate analysis of Multiple Myeloma subtype plasma cells

[Display omitted] •Characterization of Multiple Myeloma cell lines by micro-Raman spectroscopy.•Raman bands variations to identify metabolic changes.•Discrimination between Multiple Myeloma subtype plasma cells by PCA. Trusted methods for identifying different Multiple Myeloma (MM) cells and their b...

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Published in:Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy Molecular and biomolecular spectroscopy, 2021-09, Vol.258, p.119813, Article 119813
Main Authors: Bonsignore, Martina, Trusso, Sebastiano, De Pasquale, Claudia, Ferlazzo, Guido, Allegra, Alessandro, Innao, Vanessa, Musolino, Caterina, Franco, Domenico, Maria De Plano, Laura, Guglielmino, Salvatore Pietro Paolo, Neri, Fortunato, Fazio, Enza
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Language:English
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Summary:[Display omitted] •Characterization of Multiple Myeloma cell lines by micro-Raman spectroscopy.•Raman bands variations to identify metabolic changes.•Discrimination between Multiple Myeloma subtype plasma cells by PCA. Trusted methods for identifying different Multiple Myeloma (MM) cells and their biological diversity due to their immunophenotypic variety are often little detailed and difficult to find in literature. In this work, we show that micro-Raman spectroscopy can be used to highlight if there is a certain degree of distinction or correlation between the MM subtype plasmacells in relation to the cluster of differentiation (CD45+/CD38+/CD138-) and (CD45-/CD38+/CD138+). After taking samples from the bone marrow of patients with Multiple Myeloma, the PCs were sorted by flow cytometry, selecting the most common CD of the disease, i.e. CD 45, CD38 and CD138. Some spectral differences are observed comparing the Raman spectra of the two set of samples investigated. To better define in which spectral regions there are greater differences and, therefore, to which biological contributions the changes refers, we also explored the principal component analysis (PCA) of the collected Raman data. The spectral variations between the different sorted cells have been highlighted by plotting loading vectors PC1 and PC2, which shows a net differentiation between the two set of cells. Ultimately, the differences shown by PCA have been associated with the spectral variations observed and explained in terms of changes of proteins and lipid contributions. Thus, the differentiation of Multiple Myeloma subtype plasma cells by confocal micro-Raman spectroscopy can be proposed as a diagnostic tool in the speeding up of cell identification, assessing the intracellular biochemical changes that take place in cancer cells.
ISSN:1386-1425
DOI:10.1016/j.saa.2021.119813