Diagenode

Prediction of brain metastasis development with DNA methylation signatures


Jeffrey A. Zuccato et al.

Brain metastases (BMs) are the most common and among the deadliest brain tumors. Currently, there are no reliable predictors of BM development from primary cancer, which limits early intervention. Lung adenocarcinoma (LUAD) is the most common BM source and here we obtained 402 tumor and plasma samples from a large cohort of patients with LUAD with or without BM (n = 346). LUAD DNA methylation signatures were evaluated to build and validate an accurate model predicting BM development from LUAD, which was integrated with clinical factors to provide comprehensive patient-specific BM risk probabilities in a nomogram. Additionally, immune and cell interaction gene sets were differentially methylated at promoters in BM versus paired primary LUAD and had aligning dysregulation in the proteome. Immune cells were differentially abundant in BM versus LUAD. Finally, liquid biomarkers identified from methylated cell-free DNA sequenced in plasma were used to generate and validate accurate classifiers for early BM detection. Overall, LUAD methylomes can be leveraged to predict and noninvasively identify BM, moving toward improved patient outcomes with personalized treatment.

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MagMeDIP kit
IPure kit

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Published
October, 2024

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Products used in this publication

  • MagMeDIP qPCR Kit box
    C02010021
    MagMeDIP qPCR Kit
  • default alt
    C03010015
    IPure kit v2
  • Mouse IgG
    C15200081-100
    5-methylcytosine (5-mC) Antibody - clone 33D3

 


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