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We are analyzing https://link.springer.com/article/10.1007/s00401-017-1678-x.

Title:
Global epigenetic profiling identifies methylation subgroups associated with recurrence-free survival in meningioma | Acta Neuropathologica
Description:
Meningioma is the most common primary brain tumor and carries a substantial risk of local recurrence. Methylation profiles of meningioma and their clinical implications are not well understood. We hypothesized that aggressive meningiomas have unique DNA methylation patterns that could be used to better stratify patient management. Samples (n = 140) were profiled using the Illumina HumanMethylation450BeadChip. Unsupervised modeling on a training set (n = 89) identified 2 molecular methylation subgroups of meningioma (MM) with significantly different recurrence-free survival (RFS) times between the groups: a prognostically unfavorable subgroup (MM-UNFAV) and a prognostically favorable subgroup (MM-FAV). This finding was validated in the remaining 51 samples and led to a baseline meningioma methylation classifier (bMMC) defined by 283 CpG loci (283-bMMC). To further optimize a recurrence predictor, probes subsumed within the baseline classifier were subject to additional modeling using a similar training/validation approach, leading to a 64-CpG loci meningioma methylation predictor (64-MMP). After adjustment for relevant clinical variables [WHO grade, mitotic index, Simpson grade, sex, location, and copy number aberrations (CNAs)] multivariable analyses for RFS showed that the baseline methylation classifier was not significant (p = 0.0793). The methylation predictor, however, was significantly associated with tumor recurrence (p < 0.0001). CNAs were extracted from the 450k intensity profiles. Tumor samples in the MM-UNFAV subgroup showed an overall higher proportion of CNAs compared to the MM-FAV subgroup tumors and the CNAs were complex in nature. CNAs in the MM-UNFAV subgroup included recurrent losses of 1p, 6q, 14q and 18q, and gain of 1q, all of which were previously identified as indicators of poor outcome. In conclusion, our analyses demonstrate robust DNA methylation signatures in meningioma that correlate with CNAs and stratify patients by recurrence risk.
Website Age:
28 years and 1 months (reg. 1997-05-29).

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Custom-built

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🌠 Phenomenal Traffic: 5M - 10M visitors per month


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Keywords {🔍}

pubmed, article, google, scholar, cas, methylation, meningiomas, central, meningioma, cancer, jones, pfister, dna, molecular, brain, tumor, van, hovestadt, deimling, material, supplementary, aldape, recurrence, capper, analysis, acta, tumors, kool, korshunov, subgroups, distinct, classification, dois, lichter, pdf, data, olar, sulman, clinical, neurooncology, pathol, promoter, reifenberger, research, survival, wilson, subgroup, grade, cnas, nature,

Topics {✒️}

month download article/chapter multi-platform genome-wide analysis copy number aberrations clinically relevant subgroups long-term neurological problems copy-number profiling platelet-derived growth factor dna methylation profiling central nervous system long-term recurrence rates favorable long-term outcome mitogen-activated protein kinase van den berg dna methylation analysis similar training/validation approach mm-fav subgroup tumors 1093/neuonc/nov189 ozaki microarray-based svm classifiers mm-unfav subgroup showed differential dna methylation health/national cancer institute dna methylation sequencing full article pdf genome-wide signatures upa promoter methylation distinct molecular entity robust molecular subgrouping privacy choices/manage cookies clinical practice guidelines protein kinase activation 450k methylation array hollings cancer center distinct nosologic entities curry wt jr infinium humanmethylation450 beadchip natl cancer inst baseline methylation classifier german cancer network methylation-based classification stemmer-rachamimov ao article olar prognostically favorable subgroup dna methylation methylation profiling bi wl molecular pattern discovery genetic/molecular alterations biological subgroups prognostically unfavorable subgroup tert promoter mutations

Questions {❓}

  • Fernandez-Delgado M, Cernadas E, Barro S, Amorim D (2014) Do we need hundreds of classifiers to solve real world classification problems?

Schema {🗺️}

WebPage:
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         headline:Global epigenetic profiling identifies methylation subgroups associated with recurrence-free survival in meningioma
         description:Meningioma is the most common primary brain tumor and carries a substantial risk of local recurrence. Methylation profiles of meningioma and their clinical implications are not well understood. We hypothesized that aggressive meningiomas have unique DNA methylation patterns that could be used to better stratify patient management. Samples (n = 140) were profiled using the Illumina HumanMethylation450BeadChip. Unsupervised modeling on a training set (n = 89) identified 2 molecular methylation subgroups of meningioma (MM) with significantly different recurrence-free survival (RFS) times between the groups: a prognostically unfavorable subgroup (MM-UNFAV) and a prognostically favorable subgroup (MM-FAV). This finding was validated in the remaining 51 samples and led to a baseline meningioma methylation classifier (bMMC) defined by 283 CpG loci (283-bMMC). To further optimize a recurrence predictor, probes subsumed within the baseline classifier were subject to additional modeling using a similar training/validation approach, leading to a 64-CpG loci meningioma methylation predictor (64-MMP). After adjustment for relevant clinical variables [WHO grade, mitotic index, Simpson grade, sex, location, and copy number aberrations (CNAs)] multivariable analyses for RFS showed that the baseline methylation classifier was not significant (p = 0.0793). The methylation predictor, however, was significantly associated with tumor recurrence (p < 0.0001). CNAs were extracted from the 450k intensity profiles. Tumor samples in the MM-UNFAV subgroup showed an overall higher proportion of CNAs compared to the MM-FAV subgroup tumors and the CNAs were complex in nature. CNAs in the MM-UNFAV subgroup included recurrent losses of 1p, 6q, 14q and 18q, and gain of 1q, all of which were previously identified as indicators of poor outcome. In conclusion, our analyses demonstrate robust DNA methylation signatures in meningioma that correlate with CNAs and stratify patients by recurrence risk.
         datePublished:2017-01-27T00:00:00Z
         dateModified:2017-01-27T00:00:00Z
         pageStart:431
         pageEnd:444
         sameAs:https://doi.org/10.1007/s00401-017-1678-x
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            Meningioma
            Epigenetics
            DNA methylation
            Recurrence risk
            Copy number aberrations
            Molecular subgroups
            Pathology
            Neurosciences
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      headline:Global epigenetic profiling identifies methylation subgroups associated with recurrence-free survival in meningioma
      description:Meningioma is the most common primary brain tumor and carries a substantial risk of local recurrence. Methylation profiles of meningioma and their clinical implications are not well understood. We hypothesized that aggressive meningiomas have unique DNA methylation patterns that could be used to better stratify patient management. Samples (n = 140) were profiled using the Illumina HumanMethylation450BeadChip. Unsupervised modeling on a training set (n = 89) identified 2 molecular methylation subgroups of meningioma (MM) with significantly different recurrence-free survival (RFS) times between the groups: a prognostically unfavorable subgroup (MM-UNFAV) and a prognostically favorable subgroup (MM-FAV). This finding was validated in the remaining 51 samples and led to a baseline meningioma methylation classifier (bMMC) defined by 283 CpG loci (283-bMMC). To further optimize a recurrence predictor, probes subsumed within the baseline classifier were subject to additional modeling using a similar training/validation approach, leading to a 64-CpG loci meningioma methylation predictor (64-MMP). After adjustment for relevant clinical variables [WHO grade, mitotic index, Simpson grade, sex, location, and copy number aberrations (CNAs)] multivariable analyses for RFS showed that the baseline methylation classifier was not significant (p = 0.0793). The methylation predictor, however, was significantly associated with tumor recurrence (p < 0.0001). CNAs were extracted from the 450k intensity profiles. Tumor samples in the MM-UNFAV subgroup showed an overall higher proportion of CNAs compared to the MM-FAV subgroup tumors and the CNAs were complex in nature. CNAs in the MM-UNFAV subgroup included recurrent losses of 1p, 6q, 14q and 18q, and gain of 1q, all of which were previously identified as indicators of poor outcome. In conclusion, our analyses demonstrate robust DNA methylation signatures in meningioma that correlate with CNAs and stratify patients by recurrence risk.
      datePublished:2017-01-27T00:00:00Z
      dateModified:2017-01-27T00:00:00Z
      pageStart:431
      pageEnd:444
      sameAs:https://doi.org/10.1007/s00401-017-1678-x
      keywords:
         Meningioma
         Epigenetics
         DNA methylation
         Recurrence risk
         Copy number aberrations
         Molecular subgroups
         Pathology
         Neurosciences
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                  address:
                     name:Departments of Pathology and Laboratory Medicine and Neurosurgery, Medical University of South Carolina and Hollings Cancer Center, Charleston, USA
                     type:PostalAddress
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            email:[email protected]
            type:Person
            name:Khalida M. Wani
            affiliation:
                  name:The University of Texas MD Anderson Cancer Center
                  address:
                     name:Department of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Charmaine D. Wilson
            affiliation:
                  name:The University of Texas School of Nursing
                  address:
                     name:Center for Nursing Research, The University of Texas School of Nursing, Houston, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Gelareh Zadeh
            affiliation:
                  name:MacFeeters-Hamilton Brain Tumour Centre
                  address:
                     name:Princess Margaret Cancer Centre, MacFeeters-Hamilton Brain Tumour Centre, Toronto, Canada
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Franco DeMonte
            affiliation:
                  name:The University of Texas MD Anderson Cancer Center
                  address:
                     name:Department of Neurosurgery, The University of Texas MD Anderson Cancer Center, Houston, USA
                     type:PostalAddress
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            type:Person
            name:David T. W. Jones
            affiliation:
                  name:German Cancer Research Center (DKFZ), German Cancer Network (DKTK)
                  address:
                     name:Division of Pediatric Neurooncology, German Cancer Research Center (DKFZ), German Cancer Network (DKTK), Heidelberg, Germany
                     type:PostalAddress
                  type:Organization
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            name:Stefan M. Pfister
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                  name:German Cancer Research Center (DKFZ), German Cancer Network (DKTK)
                  address:
                     name:Division of Pediatric Neurooncology, German Cancer Research Center (DKFZ), German Cancer Network (DKTK), Heidelberg, Germany
                     type:PostalAddress
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                  name:Heidelberg University Hospital
                  address:
                     name:Department of Pediatric Hematology and Oncology, Heidelberg University Hospital, Heidelberg, Germany
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Erik P. Sulman
            affiliation:
                  name:The University of Texas MD Anderson Cancer Center
                  address:
                     name:Department of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, USA
                     type:PostalAddress
                  type:Organization
                  name:The University of Texas MD Anderson Cancer Center
                  address:
                     name:Departments of Radiation Oncology and Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Kenneth D. Aldape
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                  name:MacFeeters-Hamilton Brain Tumour Centre
                  address:
                     name:Princess Margaret Cancer Centre, MacFeeters-Hamilton Brain Tumour Centre, Toronto, Canada
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         name:Department of Neurosurgery, The University of Texas MD Anderson Cancer Center, Houston, USA
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      name:German Cancer Research Center (DKFZ), German Cancer Network (DKTK)
      address:
         name:Division of Pediatric Neurooncology, German Cancer Research Center (DKFZ), German Cancer Network (DKTK), Heidelberg, Germany
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         name:Division of Pediatric Neurooncology, German Cancer Research Center (DKFZ), German Cancer Network (DKTK), Heidelberg, Germany
         type:PostalAddress
      name:Heidelberg University Hospital
      address:
         name:Department of Pediatric Hematology and Oncology, Heidelberg University Hospital, Heidelberg, Germany
         type:PostalAddress
      name:The University of Texas MD Anderson Cancer Center
      address:
         name:Department of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, USA
         type:PostalAddress
      name:The University of Texas MD Anderson Cancer Center
      address:
         name:Departments of Radiation Oncology and Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, USA
         type:PostalAddress
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      affiliation:
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      name:Khalida M. Wani
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            name:The University of Texas MD Anderson Cancer Center
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            name:MacFeeters-Hamilton Brain Tumour Centre
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               type:PostalAddress
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            name:The University of Texas MD Anderson Cancer Center
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               name:Department of Neurosurgery, The University of Texas MD Anderson Cancer Center, Houston, USA
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      name:David T. W. Jones
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               name:Division of Pediatric Neurooncology, German Cancer Research Center (DKFZ), German Cancer Network (DKTK), Heidelberg, Germany
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            name:German Cancer Research Center (DKFZ), German Cancer Network (DKTK)
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               name:Division of Pediatric Neurooncology, German Cancer Research Center (DKFZ), German Cancer Network (DKTK), Heidelberg, Germany
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            type:Organization
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            address:
               name:Department of Pediatric Hematology and Oncology, Heidelberg University Hospital, Heidelberg, Germany
               type:PostalAddress
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      name:Erik P. Sulman
      affiliation:
            name:The University of Texas MD Anderson Cancer Center
            address:
               name:Department of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, USA
               type:PostalAddress
            type:Organization
            name:The University of Texas MD Anderson Cancer Center
            address:
               name:Departments of Radiation Oncology and Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, USA
               type:PostalAddress
            type:Organization
      name:Kenneth D. Aldape
      affiliation:
            name:MacFeeters-Hamilton Brain Tumour Centre
            address:
               name:Princess Margaret Cancer Centre, MacFeeters-Hamilton Brain Tumour Centre, Toronto, Canada
               type:PostalAddress
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PostalAddress:
      name:Departments of Pathology and Laboratory Medicine and Neurosurgery, Medical University of South Carolina and Hollings Cancer Center, Charleston, USA
      name:Department of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, USA
      name:Center for Nursing Research, The University of Texas School of Nursing, Houston, USA
      name:Princess Margaret Cancer Centre, MacFeeters-Hamilton Brain Tumour Centre, Toronto, Canada
      name:Department of Neurosurgery, The University of Texas MD Anderson Cancer Center, Houston, USA
      name:Division of Pediatric Neurooncology, German Cancer Research Center (DKFZ), German Cancer Network (DKTK), Heidelberg, Germany
      name:Division of Pediatric Neurooncology, German Cancer Research Center (DKFZ), German Cancer Network (DKTK), Heidelberg, Germany
      name:Department of Pediatric Hematology and Oncology, Heidelberg University Hospital, Heidelberg, Germany
      name:Department of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, USA
      name:Departments of Radiation Oncology and Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, USA
      name:Princess Margaret Cancer Centre, MacFeeters-Hamilton Brain Tumour Centre, Toronto, Canada
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External Links {🔗}(324)

Analytics and Tracking {📊}

  • Google Tag Manager

Libraries {📚}

  • Clipboard.js
  • Foundation
  • Prism.js

CDN Services {📦}

  • Crossref

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