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A high-throughput test enables specific detection of hepatocellular carcinoma

High-throughput tests for early cancer detection can revolutionize public health and reduce cancer morbidity and mortality. Here we show a DNA methylation signature for hepatocellular carcinoma (HCC) detection in liquid biopsies, distinct from normal tissues and blood profiles. We developed a classi...

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Detalles Bibliográficos
Autores principales: Cheishvili, David, Wong, Chifat, Karim, Mohammad Mahbubul, Kibria, Mohammad Golam, Jahan, Nusrat, Das, Pappu Chandra, Yousuf, Md. Abul Khair, Islam, Md. Atikul, Das, Dulal Chandra, Noor-E-Alam, Sheikh Mohammad, Szyf, Moshe, Alam, Sarwar, Khan, Wasif A., Al Mahtab, Mamun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10247794/
https://www.ncbi.nlm.nih.gov/pubmed/37286539
http://dx.doi.org/10.1038/s41467-023-39055-7
Descripción
Sumario:High-throughput tests for early cancer detection can revolutionize public health and reduce cancer morbidity and mortality. Here we show a DNA methylation signature for hepatocellular carcinoma (HCC) detection in liquid biopsies, distinct from normal tissues and blood profiles. We developed a classifier using four CpG sites, validated in TCGA HCC data. A single F12 gene CpG site effectively differentiates HCC samples from other blood samples, normal tissues, and non-HCC tumors in TCGA and GEO data repositories. The markers were validated in a separate plasma sample dataset from HCC patients and controls. We designed a high-throughput assay using next-generation sequencing and multiplexing techniques, analyzing plasma samples from 554 clinical study participants, including HCC patients, non-HCC cancers, chronic hepatitis B, and healthy controls. HCC detection sensitivity was 84.5% at 95% specificity and 0.94 AUC. Implementing this assay for high-risk individuals could significantly decrease HCC morbidity and mortality.