TY - JOUR
T1 - Validation of a lab-on-chip assay for measuring sorafenib effectiveness on hcc cell proliferation
AU - Piccinno, Emanuele
AU - Monteduro, Anna Grazia
AU - Dituri, Francesco
AU - Rizzato, Silvia
AU - Giannelli, Gianluigi
AU - Maruccio, Giuseppe
N1 - Funding Information:
Funding: This work was supported by the Italian National FISR-CIPE Project “Inno-Sense”: Development of an innovative sensing platform for on-field analysis and monitoring (delibera CIPE n.78 del 07/08/2017), by Italian National PON-AIM1800370-activity 2 (topic Health) and by the Apulia region program “RESEARCH FOR INNOVATION” (REFIN n◦ 6277F79D-UNISAL036), and Ministry of Health, “Sviluppo di una Piattaforma di Organoidi per la Medicina di Precisione in Gastroenterologia” 5/1000 project to GG.
Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/12/1
Y1 - 2021/12/1
N2 - Hepatocellular carcinoma (HCC) is a highly lethal cancer, and although a few drugs are available for treatment, therapeutic effectiveness is still unsatisfactory. New drugs are urgently needed for hepatocellular carcinoma (HCC) patients. In this context, reliable preclinical assays are of paramount importance to screen the effectiveness of new drugs and, in particular, measure their effects on HCC cell proliferation. However, cell proliferation measurement is a time-consuming and operator-dependent procedure. The aim of this study was to validate an engineered miniaturized on-chip platform for real-time, non-destructive cell proliferation assays and drug screening. The effectiveness of Sorafenib, the first-line drug mainly used for patients with advanced HCC, was tested in parallel, comparing the gold standard 96-well-plate assay and our new lab-on-chip platform. Results from the lab-on-chip are consistent in intra-assay replicates and comparable to the output of standard crystal violet proliferation assays for assessing Sorafenib effectiveness on HCC cell proliferation. The miniaturized platform presents several advantages in terms of lesser reagents consumption, operator time, and costs, as well as overcoming a number of technical and operator-dependent pitfalls. Moreover, the number of cells required is lower, a relevant issue when primary cell cultures are used. In conclusion, the availability of inexpensive on-chip assays can speed up drug development, especially by using patient-derived samples to take into account disease heterogeneity and patient-specific characteristics.
AB - Hepatocellular carcinoma (HCC) is a highly lethal cancer, and although a few drugs are available for treatment, therapeutic effectiveness is still unsatisfactory. New drugs are urgently needed for hepatocellular carcinoma (HCC) patients. In this context, reliable preclinical assays are of paramount importance to screen the effectiveness of new drugs and, in particular, measure their effects on HCC cell proliferation. However, cell proliferation measurement is a time-consuming and operator-dependent procedure. The aim of this study was to validate an engineered miniaturized on-chip platform for real-time, non-destructive cell proliferation assays and drug screening. The effectiveness of Sorafenib, the first-line drug mainly used for patients with advanced HCC, was tested in parallel, comparing the gold standard 96-well-plate assay and our new lab-on-chip platform. Results from the lab-on-chip are consistent in intra-assay replicates and comparable to the output of standard crystal violet proliferation assays for assessing Sorafenib effectiveness on HCC cell proliferation. The miniaturized platform presents several advantages in terms of lesser reagents consumption, operator time, and costs, as well as overcoming a number of technical and operator-dependent pitfalls. Moreover, the number of cells required is lower, a relevant issue when primary cell cultures are used. In conclusion, the availability of inexpensive on-chip assays can speed up drug development, especially by using patient-derived samples to take into account disease heterogeneity and patient-specific characteristics.
KW - Cell proliferation
KW - Drug screening
KW - Electrochemical impedance spectroscopy
KW - Hepatocellular carcinoma
KW - Lab-on-chip
KW - Microfluidics
KW - On-chip assays
KW - Sorafenib
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U2 - 10.3390/ijms222313090
DO - 10.3390/ijms222313090
M3 - Article
AN - SCOPUS:85120558390
SN - 1661-6596
VL - 22
JO - International Journal of Molecular Sciences
JF - International Journal of Molecular Sciences
IS - 23
M1 - 13090
ER -