Noninvasive early detection of colorectal cancer by hypermethylation of the LINC00473 promoter in plasma cell-free DNA

Background: Current noninvasive assays have limitations in the early detection of colorectal cancer. We evaluated the clinical utility of promoter methylation of the long noncoding RNA LINC00473 as a noninvasive biomarker to detect colorectal cancer and associated precancerous lesions. Methods: We e...

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Detalhes bibliográficos
Autores: Ruiz Bañobre, Juan|||0000-0003-0755-4295, Rodríguez Casanova, Aitor|||0000-0002-9828-3613, Costa-Fraga, Nicolás|||0000-0002-0869-8509, Bao Caamano, Aida, Álvarez Castro, Ana, Carreras Presas, Martín, Brozos Vázquez, Elena, Vidal Insua, Yolanda, Vázquez Rivera, Francisca, Candamio Folgar, Sonia|||0000-0003-4007-5990, Mosquera Presedo, Manuel|||0000-0002-9802-1082, Lago Lestón, Ramón M.|||0000-0002-1166-7754, Muinelo-Romay, Laura|||0000-0002-7456-7531, Vázquez Bueno, José Ángel, Sanz Pamplona, Rebeca|||0000-0002-2187-3527, Moreno Aguado, Victor Raul|||0000-0002-2818-5487, Goel, Ajay|||0000-0003-1396-6341, Castillo, Lourdes, Martín, Ana C., Arroyo, Rocío, Esteller, M.|||0000-0003-4490-6093, Crujeiras, Ana B.|||0000-0003-4392-0301, López López, Rafael|||0000-0003-1315-655X, Diaz-Lagares, Angel|||0000-0002-9114-9227
Formato: artículo
Fecha de publicación:2022
País:España
Recursos:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:270587
Acesso em linha:https://ddd.uab.cat/record/270587
https://dx.doi.org/urn:doi:10.1186/s13148-022-01302-x
Access Level:acceso abierto
Palavra-chave:DNA methylation
LINC00473
Cell-free DNA
Early detection
Colorectal cancer
Descrição
Resumo:Background: Current noninvasive assays have limitations in the early detection of colorectal cancer. We evaluated the clinical utility of promoter methylation of the long noncoding RNA LINC00473 as a noninvasive biomarker to detect colorectal cancer and associated precancerous lesions. Methods: We evaluated the epigenetic regulation of LINC00473 through promoter hypermethylation in colorectal cancer cell lines using bisulfite genomic sequencing and expression analyses. DNA methylation of LINC00473 was analyzed in primary colorectal tumors using 450K arrays and RNA-seq from The Cancer Genome Atlas (TCGA). Tissue-based findings were validated in several independent cohorts of colorectal cancer and advanced colorectal polyp patients by pyrosequencing. We explored the clinical utility of LINC00473 methylation for the early detection of colorectal cancer in plasma cell-free DNA by quantitative methylation-specific PCR and droplet digital PCR. Results: LINC00473 showed transcriptionally silencing due to promoter hypermethylation in colorectal cancer cell lines and primary tumors. Methylation of the LINC00473 promoter accurately detected primary colorectal tumors in two independent clinical cohorts, with areas under the receiver operating characteristic curves (AUCs) of 0.94 and 0.89. This biomarker also identified advanced colorectal polyps from two other tissue-based clinical cohorts with high diagnostic accuracy (AUCs of 0.99 and 0.78). Finally, methylation analysis of the LINC00473 promoter in plasma cell-free DNA accurately identified patients with colorectal cancer and advanced colorectal polyps (AUCs of 0.88 and 0.84, respectively), which was confirmed in an independent cohort of patients. Conclusions: Hypermethylation of the LINC00473 promoter is a new promising biomarker for noninvasive early detection of colorectal cancer and related precancerous lesions.