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Implications of DNA Methylation Classification in Diagnosing Ependymoma.
Abe, Eiji; Suzuki, Mario; Ichimura, Koichi; Arakawa, Atsushi; Satomi, Kaishi; Ogino, Ikuko; Hara, Takeshi; Iwamuro, Hirokazu; Ohara, Yukoh; Kondo, Akihide.
Affiliation
  • Abe E; Department of Neurosurgery, Juntendo University Graduate School of Medicine, Tokyo, Japan. Electronic address: eijiabe@juntendo.ac.jp.
  • Suzuki M; Department of Neurosurgery, Juntendo University Graduate School of Medicine, Tokyo, Japan.
  • Ichimura K; Department of Neurosurgery, Juntendo University Graduate School of Medicine, Tokyo, Japan; Department of Brain Disease Translational Research, Juntendo University Graduate School of Medicine, Tokyo, Japan.
  • Arakawa A; Department of Human Pathology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
  • Satomi K; Department of Pathology, Kyorin University Faculty of Medicine, Tokyo, Japan.
  • Ogino I; Department of Neurosurgery, Juntendo University Graduate School of Medicine, Tokyo, Japan.
  • Hara T; Department of Neurosurgery, Juntendo University Graduate School of Medicine, Tokyo, Japan.
  • Iwamuro H; Department of Neurosurgery, Juntendo University Graduate School of Medicine, Tokyo, Japan.
  • Ohara Y; Department of Neurosurgery, Juntendo University Graduate School of Medicine, Tokyo, Japan.
  • Kondo A; Department of Neurosurgery, Juntendo University Graduate School of Medicine, Tokyo, Japan.
World Neurosurg ; 185: e1019-e1029, 2024 05.
Article in En | MEDLINE | ID: mdl-38479644
ABSTRACT

BACKGROUND:

Ependymoma is a central nervous system (CNS) tumor that arises from the ependymal cells of the brain's ventricles and spinal cord. The histopathology of ependymomas is indistinguishable regardless of the site of origin, and the prognosis varies. Recent studies have revealed that the development site and prognosis reflect the genetic background. In this study, we used genome-wide DNA methylation array analysis to investigate the epigenetic background of ependymomas from different locations treated at our hospital.

METHODS:

Four cases of posterior fossa ependymomas and 11 cases of spinal ependymomas were analyzed.

RESULTS:

DNA methylation profiling using the DKFZ methylation classifier showed that the methylation diagnoses of the 2 cases differed from the histopathological diagnoses, and 2 cases could not be classified. Tumor that spread from the brain to the spinal cord was molecularly distinguishable from other primary spinal tumors.

CONCLUSIONS:

Although adding DNA methylation classification to conventional diagnostic methods may be helpful, the diagnosis in some cases remains undetermined. This may affect decision-making regarding treatment strategies and follow-up. Further investigations are required to improve the diagnostic accuracy of these tumors.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Spinal Cord Neoplasms / DNA Methylation / Ependymoma Limits: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Male / Middle aged Language: En Journal: World Neurosurg / World neurosurgery (Online) Journal subject: NEUROCIRURGIA Year: 2024 Document type: Article Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Spinal Cord Neoplasms / DNA Methylation / Ependymoma Limits: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Male / Middle aged Language: En Journal: World Neurosurg / World neurosurgery (Online) Journal subject: NEUROCIRURGIA Year: 2024 Document type: Article Country of publication: