4.8 Article

The integrated genomic and epigenomic landscape of brainstem glioma

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NATURE COMMUNICATIONS
卷 11, 期 1, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/s41467-020-16682-y

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资金

  1. National Key Technology Research and Development Program of the Ministry of Science and Technology of China [2014BAI04B01, 2015BAI12B04]
  2. Beijing Municipal Administration of Hospitals Clinical Medicine Development of Special Funding Support [ZYLX201608]
  3. National Natural Science Foundation of China [81872048]
  4. Beijing Municipal Natural Science Foundation [7161004]
  5. 2016 Development Project of Science and Technology Innovation Base [206028]
  6. Beijing Municipal Special Funds for Medical Research [JingYiYan 2018-7]
  7. Duke Brain Tumor Center Grant
  8. Zachem Family Fund

向作者/读者索取更多资源

Brainstem gliomas are a heterogeneous group of tumors that encompass both benign tumors cured with surgical resection and highly lethal cancers with no efficacious therapies. We perform a comprehensive study incorporating epigenetic and genomic analyses on a large cohort of brainstem gliomas, including Diffuse Intrinsic Pontine Gliomas. Here we report, from DNA methylation data, distinct clusters termed H3-Pons, H3-Medulla, IDH, and PA-like, each associated with unique genomic and clinical profiles. The majority of tumors within H3-Pons and-H3-Medulla harbors H3F3A mutations but shows distinct methylation patterns that correlate with anatomical localization within the pons or medulla, respectively. Clinical data show significantly different overall survival between these clusters, and pathway analysis demonstrates different oncogenic mechanisms in these samples. Our findings indicate that the integration of genetic and epigenetic data can facilitate better understanding of brainstem gliomagenesis and classification, and guide future studies for the development of novel treatments for this disease. Brainstem gliomas are heterogenous in terms of clinical outcome and disease etiology. Here, the authors present a genetic and epigenetic landscape of brainstem gliomas, finding distinct epigenetic clusters associated with unique genetic and clinical profiles.

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