IDEAS home Printed from https://ideas.repec.org/a/plo/pone00/0047839.html
   My bibliography  Save this article

G-Cimp Status Prediction Of Glioblastoma Samples Using mRNA Expression Data

Author

Listed:
  • Mehmet Baysan
  • Serdar Bozdag
  • Margaret C Cam
  • Svetlana Kotliarova
  • Susie Ahn
  • Jennifer Walling
  • Jonathan K Killian
  • Holly Stevenson
  • Paul Meltzer
  • Howard A Fine

Abstract

Glioblastoma Multiforme (GBM) is a tumor with high mortality and no known cure. The dramatic molecular and clinical heterogeneity seen in this tumor has led to attempts to define genetically similar subgroups of GBM with the hope of developing tumor specific therapies targeted to the unique biology within each of these subgroups. Recently, a subset of relatively favorable prognosis GBMs has been identified. These glioma CpG island methylator phenotype, or G-CIMP tumors, have distinct genomic copy number aberrations, DNA methylation patterns, and (mRNA) expression profiles compared to other GBMs. While the standard method for identifying G-CIMP tumors is based on genome-wide DNA methylation data, such data is often not available compared to the more widely available gene expression data. In this study, we have developed and evaluated a method to predict the G-CIMP status of GBM samples based solely on gene expression data.

Suggested Citation

  • Mehmet Baysan & Serdar Bozdag & Margaret C Cam & Svetlana Kotliarova & Susie Ahn & Jennifer Walling & Jonathan K Killian & Holly Stevenson & Paul Meltzer & Howard A Fine, 2012. "G-Cimp Status Prediction Of Glioblastoma Samples Using mRNA Expression Data," PLOS ONE, Public Library of Science, vol. 7(11), pages 1-10, November.
  • Handle: RePEc:plo:pone00:0047839
    DOI: 10.1371/journal.pone.0047839
    as

    Download full text from publisher

    File URL: https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0047839
    Download Restriction: no

    File URL: https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0047839&type=printable
    Download Restriction: no

    File URL: https://libkey.io/10.1371/journal.pone.0047839?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    References listed on IDEAS

    as
    1. Sevin Turcan & Daniel Rohle & Anuj Goenka & Logan A. Walsh & Fang Fang & Emrullah Yilmaz & Carl Campos & Armida W. M. Fabius & Chao Lu & Patrick S. Ward & Craig B. Thompson & Andrew Kaufman & Olga Gur, 2012. "IDH1 mutation is sufficient to establish the glioma hypermethylator phenotype," Nature, Nature, vol. 483(7390), pages 479-483, March.
    2. Nicholas F Marko & John Quackenbush & Robert J Weil, 2011. "Why Is There a Lack of Consensus on Molecular Subgroups of Glioblastoma? Understanding the Nature of Biological and Statistical Variability in Glioblastoma Expression Data," PLOS ONE, Public Library of Science, vol. 6(7), pages 1-19, July.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Anna M Dahlin & Carl Wibom & Soma Ghasimi & Thomas Brännström & Ulrika Andersson & Beatrice Melin, 2016. "Relation between Established Glioma Risk Variants and DNA Methylation in the Tumor," PLOS ONE, Public Library of Science, vol. 11(10), pages 1-14, October.
    2. Bar Haim Y. & Booth James G. & Wells Martin T., 2012. "A Mixture-Model Approach for Parallel Testing for Unequal Variances," Statistical Applications in Genetics and Molecular Biology, De Gruyter, vol. 11(1), pages 1-21, January.
    3. Siobhan Conroy & Frank A E Kruyt & Justin V Joseph & Veerakumar Balasubramaniyan & Krishna P Bhat & Michiel Wagemakers & Roelien H Enting & Annemiek M E Walenkamp & Wilfred F A den Dunnen, 2014. "Subclassification of Newly Diagnosed Glioblastomas through an Immunohistochemical Approach," PLOS ONE, Public Library of Science, vol. 9(12), pages 1-21, December.
    4. Walid K. Chatila & Henry Walch & Jaclyn F. Hechtman & Sydney M. Moyer & Valeria Sgambati & David M. Faleck & Amitabh Srivastava & Laura Tang & Jamal Benhamida & Dorina Ismailgeci & Carl Campos & Fan W, 2023. "Integrated clinical and genomic analysis identifies driver events and molecular evolution of colitis-associated cancers," Nature Communications, Nature, vol. 14(1), pages 1-13, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:plo:pone00:0047839. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: plosone (email available below). General contact details of provider: https://journals.plos.org/plosone/ .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.