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Longitudinal Circulating Levels of miR-23b-3p, miR-126-3p and lncRNA GAS5 in HCC Patients Treated with Sorafenib

Authors :
Michele Manganelli
Ilaria Grossi
Manuela Ferracin
Paola Guerriero
Massimo Negrini
Michele Ghidini
Chiara Senti
Margherita Ratti
Claudio Pizzo
Rodolfo Passalacqua
Sarah Molfino
Gianluca Baiocchi
Nazario Portolani
Eleonora Marchina
Giuseppina De Petro
Alessandro Salvi
Source :
Biomedicines, Vol 9, Iss 7, p 813 (2021)
Publication Year :
2021
Publisher :
MDPI AG, 2021.

Abstract

Human hepatocellular carcinoma (HCC) is the most frequent primary tumor of the liver and the third cause of cancer-related deaths. The multikinase inhibitor sorafenib is a systemic drug for unresectable HCC. The identification of molecular biomarkers for the early diagnosis of HCC and responsiveness to treatment are needed. In this work, we performed an exploratory study to investigate the longitudinal levels of cell-free long ncRNA GAS5 and microRNAs miR-126-3p and -23b-3p in a cohort of 7 patients during the period of treatment with sorafenib. We used qPCR to measure the amounts of GAS5 and miR-126-3p and droplet digital PCR (ddPCR) to measure the levels of miR-23b-3p. Patients treated with sorafenib displayed variable levels of GAS5, miR-126-3p and miR-23b-3p at different time-points of follow-up. miR-23b-3p was further measured by ddPCR in 37 healthy individuals and 25 untreated HCC patients. The amount of miR-23b-3p in the plasma of untreated HCC patients was significantly downregulated if compared to healthy individuals. The ROC curve analysis underlined its diagnostic relevance. In conclusion, our results highlight a potential clinical significance of circulating miR-23b-3p and an exploratory observation on the longitudinal plasmatic levels of GAS5, miR-126-3p and miR-23b-3p during sorafenib treatment.

Details

Language :
English
ISSN :
22279059
Volume :
9
Issue :
7
Database :
Directory of Open Access Journals
Journal :
Biomedicines
Publication Type :
Academic Journal
Accession number :
edsdoj.84fb4fbdb40a4d67baf615514974a709
Document Type :
article
Full Text :
https://doi.org/10.3390/biomedicines9070813