Author
Listed:
- Lee H. Chen
(Duke University Medical Center
Duke University Medical Center)
- Changcun Pan
(Capital Medical University
China National Clinical Research Center for Neurological Diseases
Beijing Key Laboratory of Brain Tumor)
- Bill H. Diplas
(Duke University Medical Center
Duke University Medical Center)
- Cheng Xu
(Duke University Medical Center
Duke University Medical Center
Capital Medical University)
- Landon J. Hansen
(Duke University Medical Center
Duke University Medical Center)
- Yuliang Wu
(Capital Medical University)
- Xin Chen
(Capital Medical University)
- Yibo Geng
(Capital Medical University)
- Tao Sun
(Capital Medical University)
- Yu Sun
(Capital Medical University)
- Peng Zhang
(Capital Medical University)
- Zhen Wu
(Capital Medical University)
- Junting Zhang
(Capital Medical University)
- Deling Li
(Capital Medical University)
- Yang Zhang
(Capital Medical University)
- Wenhao Wu
(Capital Medical University)
- Yu Wang
(Capital Medical University)
- Guangyu Li
(Genetron Health (Beijing) Co. Ltd)
- Jie Yang
(Genetron Health (Beijing) Co. Ltd)
- Xiaoyue Wang
(Peking Union Medical College)
- Ce Xu
(Genetron Health (Beijing) Co. Ltd)
- Sizhen Wang
(Genetron Health (Beijing) Co. Ltd)
- Matthew S. Waitkus
(Duke University Medical Center
Duke University Medical Center)
- Yiping He
(Duke University Medical Center
Duke University Medical Center)
- Roger E. McLendon
(Duke University Medical Center)
- David M. Ashley
(Duke University Medical Center)
- Hai Yan
(Duke University Medical Center
Duke University Medical Center)
- Liwei Zhang
(Capital Medical University
China National Clinical Research Center for Neurological Diseases
Beijing Key Laboratory of Brain Tumor)
Abstract
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.
Suggested Citation
Lee H. Chen & Changcun Pan & Bill H. Diplas & Cheng Xu & Landon J. Hansen & Yuliang Wu & Xin Chen & Yibo Geng & Tao Sun & Yu Sun & Peng Zhang & Zhen Wu & Junting Zhang & Deling Li & Yang Zhang & Wenha, 2020.
"The integrated genomic and epigenomic landscape of brainstem glioma,"
Nature Communications, Nature, vol. 11(1), pages 1-11, December.
Handle:
RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-16682-y
DOI: 10.1038/s41467-020-16682-y
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