Transcriptional analyses of adult and pediatric adamantinomatous craniopharyngioma reveals similar expression signatures regarding potential therapeutic targets.

dc.contributor.author

Prince, Eric

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Whelan, Ros

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Donson, Andrew

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Staulcup, Susan

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Hengartner, Astrid

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Vijmasi, Trinka

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Agwu, Chibueze

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Lillehei, Kevin O

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Foreman, Nicholas K

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Johnston, James M

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Massimi, Luca

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Anderson, Richard CE

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Souweidane, Mark M

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Naftel, Robert P

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Limbrick, David D

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Grant, Gerald

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Niazi, Toba N

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Dudley, Roy

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Kilburn, Lindsay

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Jackson, Eric M

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Jallo, George I

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Ginn, Kevin

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Smith, Amy

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Chern, Joshua J

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Lee, Amy

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Drapeau, Annie

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Krieger, Mark D

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Handler, Michael H

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Hankinson, Todd C

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Advancing Treatment for Pediatric Craniopharyngioma Consortium

dc.date.accessioned

2022-09-30T17:51:46Z

dc.date.available

2022-09-30T17:51:46Z

dc.date.issued

2020-05

dc.date.updated

2022-09-30T17:51:43Z

dc.description.abstract

Adamantinomatous craniopharyngioma (ACP) is a biologically benign but clinically aggressive lesion that has a significant impact on quality of life. The incidence of the disease has a bimodal distribution, with peaks occurring in children and older adults. Our group previously published the results of a transcriptome analysis of pediatric ACPs that identified several genes that were consistently overexpressed relative to other pediatric brain tumors and normal tissue. We now present the results of a transcriptome analysis comparing pediatric to adult ACP to identify biological differences between these groups that may provide novel therapeutic insights or support the assertion that potential therapies identified through the study of pediatric ACP may also have a role in adult ACP. Using our compiled transcriptome dataset of 27 pediatric and 9 adult ACPs, obtained through the Advancing Treatment for Pediatric Craniopharyngioma Consortium, we interrogated potential age-related transcriptional differences using several rigorous mathematical analyses. These included: canonical differential expression analysis; divisive, agglomerative, and probabilistic based hierarchical clustering; information theory based characterizations; and the deep learning approach, HD Spot. Our work indicates that there is no therapeutically relevant difference in ACP gene expression based on age. As such, potential therapeutic targets identified in pediatric ACP are also likely to have relvance for adult patients.

dc.identifier

10.1186/s40478-020-00939-0

dc.identifier.issn

2051-5960

dc.identifier.issn

2051-5960

dc.identifier.uri

https://hdl.handle.net/10161/25890

dc.language

eng

dc.publisher

Springer Science and Business Media LLC

dc.relation.ispartof

Acta neuropathologica communications

dc.relation.isversionof

10.1186/s40478-020-00939-0

dc.subject

Advancing Treatment for Pediatric Craniopharyngioma Consortium

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Humans

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Craniopharyngioma

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Pituitary Neoplasms

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Gene Expression Profiling

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Computational Biology

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Adult

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Middle Aged

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Child

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Transcriptome

dc.title

Transcriptional analyses of adult and pediatric adamantinomatous craniopharyngioma reveals similar expression signatures regarding potential therapeutic targets.

dc.type

Journal article

duke.contributor.orcid

Grant, Gerald|0000-0002-2651-4603

pubs.begin-page

68

pubs.issue

1

pubs.organisational-group

Duke

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School of Medicine

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Clinical Science Departments

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Institutes and Centers

pubs.organisational-group

Duke Cancer Institute

pubs.organisational-group

Neurosurgery

pubs.publication-status

Published

pubs.volume

8

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