posted on 2020-11-18, 07:13authored byMario Russo, Luca Tirinato, Francesca Scionti, Maria Laura Coluccio, Gerardo Perozziello, Caterina Riillo, Vincenzo Mollace, Santo Gratteri, Natalia Malara, Maria Teresa Di Martino, Giuseppe Viglietto, Pierosandro Tagliaferri, Pierfrancesco Tassone, Marco Rossi, Patrizio Candeloro
Multiple
myeloma (MM) is a hematological malignancy characterized
by abnormal plasma cell proliferation within the bone marrow which
leads to progressive bone marrow failure, skeletal osteolytic lesions,
and renal insufficiency, thus severely affecting the quality of life.
MM is always preceded by monoclonal gammopathy of uncertain significance
(MGUS), which progresses to asymptomatic-MM (aMM) or symptomatic-MM
(sMM) at a rate of 1% per year. Despite impressive progress in the
therapy of the disease, MM remains incurable. Based on these premises,
the identification of biomarkers of MGUS progression to MM is a crucial
issue in disease management. In this regard, exosomes (EXs) and their
precious biomolecular cargo could play a pivotal role in MM detection,
stratification, and follow-up. Raman spectroscopy, a label- and manipulation-free
technique, and its enhanced version, surface-enhanced Raman spectroscopy
(SERS), have been used for characterizing MGUS, aMM, and sMM patient-derived
EXs. Here, we have demonstrated the capability of Raman spectroscopy
for discriminating EXs along the progression from MGUS to aMM and
sMM, thus providing useful clinical indications for patient care.
The used SERS devices, based on random nanostructures, have shown
good potential in terms of sensitivity, but further developments are
needed for achieving reproducible and quantitative SERS results.