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Yang, Rongxi; Pfütze, Katrin; Zucknick, Manuela; Sutter, Christian; Wappenschmidt, Barbara; Marme, Frederik; Qu, Bin; Cuk, Katarina; Engel, Christoph; Schott, Sarah; Schneeweiss, Andreas; Brenner, Hermann; Claus, Rainer; Plass, Christoph; Bugert, Peter; Hoth, Markus; Sohn, Christof; Schmutzler, Rita; Bartram, Claus R.; Burwinkel, Barbara

DNA methylation array analyses identified breast cancer‐associated HYAL2 methylation in peripheral blood

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  • Media type: E-Article
  • Title: DNA methylation array analyses identified breast cancer‐associated HYAL2 methylation in peripheral blood
  • Contributor: Yang, Rongxi; Pfütze, Katrin; Zucknick, Manuela; Sutter, Christian; Wappenschmidt, Barbara; Marme, Frederik; Qu, Bin; Cuk, Katarina; Engel, Christoph; Schott, Sarah; Schneeweiss, Andreas; Brenner, Hermann; Claus, Rainer; Plass, Christoph; Bugert, Peter; Hoth, Markus; Sohn, Christof; Schmutzler, Rita; Bartram, Claus R.; Burwinkel, Barbara
  • imprint: Wiley, 2015
  • Published in: International Journal of Cancer
  • Language: English
  • DOI: 10.1002/ijc.29205
  • ISSN: 0020-7136; 1097-0215
  • Keywords: Cancer Research ; Oncology
  • Origination:
  • Footnote:
  • Description: <jats:p>Breast cancer (BC) is the leading cause of cancer‐related mortality in women worldwide. Changes in DNA methylation in peripheral blood could be associated with malignancy at early stage. However, the BC‐associated DNA methylation signatures in peripheral blood were largely unknown. Here, we performed a genome‐wide methylation screening and identified a BC‐associated differentially methylated CpG site cg27091787 in the hyaluronoglucosaminidase 2 gene (<jats:italic>HYAL2</jats:italic>) (discovery round with 72 BC case and 24 controls: <jats:italic>p</jats:italic> = 2.61 × 10<jats:sup>−9</jats:sup> adjusted for cell‐type proportions). The substantially decreased methylation of cg27091787 in BC cases was confirmed in two validation rounds (first validation round with 338 BC case and 507 controls: <jats:italic>p</jats:italic> &lt; 0.0001; second validation round with 189 BC case and 189 controls: <jats:italic>p</jats:italic> &lt; 0.0001). In addition to cg27091787, the decreased methylation of a 650‐bp CpG island shore of <jats:italic>HYAL2</jats:italic> was also associated with increased risk of BC. Moreover, the expression and methylation of <jats:italic>HYAL2</jats:italic> were inversely correlated with a <jats:italic>p</jats:italic>‐value of 0.006. To note, the BC‐associated decreased <jats:italic>HYAL2</jats:italic> methylation was replicated in the T‐cell fraction (<jats:italic>p</jats:italic> = 0.034). The cg27091787 methylation level enabled a powerful discrimination of early‐stage BC cases (stages 0 and I) from healthy controls [area under curve (AUC) = 0.89], and was robust for the detection of BC in younger women as well (age &lt; 50, AUC = 0.87). Our study reveals a strong association between decreased <jats:italic>HYAL2</jats:italic> methylation in peripheral blood and BC, and provides a promising blood‐based marker for the detection of early BC.</jats:p>
  • Access State: Open Access