Your browser doesn't support javascript.
loading
Brain metastasis DNA methylomes, a novel resource for the identification of biological and clinical features.
Salomon, Matthew P; Orozco, Javier I J; Wilmott, James S; Hothi, Parvinder; Manughian-Peter, Ayla O; Cobbs, Charles S; Scolyer, Richard A; Hoon, Dave S B; Marzese, Diego M.
Affiliation
  • Salomon MP; Department of Translational Molecular Medicine, John Wayne Cancer Institute at Providence Saint John's Health Center, Santa Monica, CA 90404, USA.
  • Orozco JIJ; Department of Translational Molecular Medicine, John Wayne Cancer Institute at Providence Saint John's Health Center, Santa Monica, CA 90404, USA.
  • Wilmott JS; Melanoma Institute Australia, The University of Sydney, Camperdown, NSW, 2065, Australia.
  • Hothi P; Ben & Catherine Ivy Center for Advanced Brain Tumor Treatment, Swedish Neuroscience Institute, Seattle, WA 98122, USA.
  • Manughian-Peter AO; Department of Translational Molecular Medicine, John Wayne Cancer Institute at Providence Saint John's Health Center, Santa Monica, CA 90404, USA.
  • Cobbs CS; Ben & Catherine Ivy Center for Advanced Brain Tumor Treatment, Swedish Neuroscience Institute, Seattle, WA 98122, USA.
  • Scolyer RA; Melanoma Institute Australia, The University of Sydney, Camperdown, NSW, 2065, Australia.
  • Hoon DSB; Sydney Medical School, The University of Sydney, Camperdown, NSW, 2006, Australia.
  • Marzese DM; Royal Prince Alfred Hospital, Sydney, New South Wales, 2050, Australia.
Sci Data ; 5: 180245, 2018 11 06.
Article in En | MEDLINE | ID: mdl-30398472
ABSTRACT
Brain metastases (BM) are one the most lethal and poorly managed clinical complications in cancer patients. These secondary tumors represent the most common intracranial neoplasm in adults, most frequently originating from lung cancer, breast cancer, and cutaneous melanoma. In primary brain tumors, such as gliomas, recent advances in DNA methylation profiling have allowed for a comprehensive molecular classification. Such data provide prognostic information, in addition to helping predict patient response to specific systemic therapies. However, epigenetic alterations of metastatic brain tumors with specific biological and translational relevance still require much further exploration. Using the widely employed Illumina Infinium HumanMethylation 450K platform, we have generated a cohort of genome-wide DNA methylomes from ninety-six needle-dissected BM specimens from patients with lung cancer, breast cancer, and cutaneous melanoma with clinical, pathological, and demographic annotations. This resource offers an unprecedented and unique opportunity to identify novel DNA methylation features influencing the behavior of brain metastasis, and thus accelerate the discovery of BM-specific theranostic epigenetic alterations.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain Neoplasms / DNA Methylation / Epigenomics Type of study: Diagnostic_studies Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: Sci Data Year: 2018 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain Neoplasms / DNA Methylation / Epigenomics Type of study: Diagnostic_studies Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: Sci Data Year: 2018 Document type: Article Affiliation country: United States