Digital multiplexed analysis of circular RNAs in FFPE and fresh non-small cell lung cancer specimens

Although many studies highlight the implication of circular RNAs (circRNAs) in carcinogenesis and tumor progression, their potential as cancer biomarkers has not yet been fully explored in the clinic due to the limitations of current quantification methods. Here, we report the use of the nCounter pl...

Descripción completa

Detalles Bibliográficos
Autores: Pedraz-Valdunciel, Carlos|||0000-0002-3163-2444, Giannoukakos, Stavros|||0000-0001-8190-4199, Potie, Nicolas, Giménez-Capitán, Ana|||0000-0003-2575-1225, Huang, Chung-Ying, Hackenberg, Michael|||0000-0003-2248-3114, Fernandez-Hilario, Alberto, Bracht, Jillian|||0000-0001-9552-3960, Filipska, Martyna|||0000-0001-9947-4561, Aldeguer, Erika, Rodríguez, Sonia, Bivona, Trever, Warren, Sarah, Aguado, Cristina, Ito, Masaoki, Aguilar-Hernández, Andrés, Molina Vila, Miguel Ángel|||0000-0001-8866-9881, Rosell, Rafael|||0000-0003-0817-3400
Tipo de recurso: artículo
Fecha de publicación:2022
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:292942
Acceso en línea:https://ddd.uab.cat/record/292942
https://dx.doi.org/urn:doi:10.1002/1878-0261.13182
Access Level:acceso abierto
Palabra clave:Biomarkers
Cancer
Circrna
Diagnosis
Ncounter
NSCLC
Descripción
Sumario:Although many studies highlight the implication of circular RNAs (circRNAs) in carcinogenesis and tumor progression, their potential as cancer biomarkers has not yet been fully explored in the clinic due to the limitations of current quantification methods. Here, we report the use of the nCounter platform as a valid technology for the analysis of circRNA expression patterns in non-small cell lung cancer (NSCLC) specimens. Under this context, our custom-made circRNA panel was able to detect circRNA expression both in NSCLC cells and formalin-fixed paraffin-embedded (FFPE) tissues. CircFUT8 was overexpressed in NSCLC, contrasting with circEPB41L2, circBNC2, and circSOX13 downregulation even at the early stages of the disease. Machine learning (ML) approaches from different paradigms allowed discrimination of NSCLC from nontumor controls (NTCs) with an 8-circRNA signature. An additional 4-circRNA signature was able to classify early-stage NSCLC samples from NTC, reaching a maximum area under the ROC curve (AUC) of 0.981. Our results not only present two circRNA signatures with diagnosis potential but also introduce nCounter processing following ML as a feasible protocol for the study and development of circRNA signatures for NSCLC. Aberrant circular RNA (circRNA) expression is present in lung cancer. Using nCounter with machine learning, we discovered two signatures able to discriminate FFPE lung cancer samples from controls even at early stage. Our results not only highlight the potential of circRNAs as lung cancer biomarkers but also introduce nCounter as a suitable platform for circRNA expression studies in these samples.