Ontology highlight
ABSTRACT:
Methods: Herein, we sought to identify and validate DNA methylation-based biomarkers for early detection and prediction of response to therapy in ECa patients. Promoter methylation levels were assessed in a series of treatment-naïve ECa, post-neoadjuvant treatment ECa, and normal esophagus tissues, using quantitative methylation-specific PCR for COL14A1, GPX3, and ZNF569.
Results: ZNF569 methylation (ZNF569me) levels significantly differed between ECa and normal samples (p
Conclusion: The biomarker potential of a specific panel of methylated genes for ECa was confirmed. These might prove useful for early detection and might allow for the identification of minimal residual disease after adjuvant therapy.
SUBMITTER: Salta S
PROVIDER: S-EPMC7691099 | biostudies-literature | 2020 Nov
REPOSITORIES: biostudies-literature
Salta Sofia S Macedo-Silva Catarina C Miranda-Gonçalves Vera V Lopes Nair N Gigliano Davide D Guimarães Rita R Farinha Mónica M Sousa Olga O Henrique Rui R Jerónimo Carmen C
Biomarker research 20201125 1
<h4>Background</h4>Esophageal cancer (ECa) is the 7th most incident cancer and the 6th leading cause of cancer-related death. Most patients are diagnosed with locally advanced or metastatic disease, enduring poor survival. Biomarkers enabling early cancer detection may improve patient management, treatment effectiveness, and survival, are urgently needed. In this context, epigenetic-based biomarkers such as DNA methylation are potential candidates.<h4>Methods</h4>Herein, we sought to identify an ...[more]