IL-13 receptors as possible therapeutic targets in diffuse intrinsic pontine glioma.

Diffuse intrinsic pontine glioma (DIPG) is a universally fatal childhood cancer of the brain. Despite the introduction of conventional chemotherapy and radiotherapy, improvements in survival have been marginal and long-term survivorship is uncommon. Thus, new targets for therapeutics are critically...

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Main Authors: Noah E Berlow, Matthew N Svalina, Michael J Quist, Teagan P Settelmeyer, Viktor Zherebitskiy, Mari Kogiso, Lin Qi, Yuchen Du, Cynthia E Hawkins, Esther Hulleman, Xiao-Nan Li, Sakir H Gultekin, Charles Keller
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5886401?pdf=render
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author Noah E Berlow
Matthew N Svalina
Michael J Quist
Teagan P Settelmeyer
Viktor Zherebitskiy
Mari Kogiso
Lin Qi
Yuchen Du
Cynthia E Hawkins
Esther Hulleman
Xiao-Nan Li
Sakir H Gultekin
Charles Keller
author_facet Noah E Berlow
Matthew N Svalina
Michael J Quist
Teagan P Settelmeyer
Viktor Zherebitskiy
Mari Kogiso
Lin Qi
Yuchen Du
Cynthia E Hawkins
Esther Hulleman
Xiao-Nan Li
Sakir H Gultekin
Charles Keller
author_sort Noah E Berlow
collection DOAJ
description Diffuse intrinsic pontine glioma (DIPG) is a universally fatal childhood cancer of the brain. Despite the introduction of conventional chemotherapy and radiotherapy, improvements in survival have been marginal and long-term survivorship is uncommon. Thus, new targets for therapeutics are critically needed. Early phase clinical trials exploring molecularly-targeted therapies against the epidermal growth factor receptor (EGFR) and novel immunotherapies targeting interleukin receptor-13α2 (IL-13Rα2) have demonstrated activity in this disease. To identify additional therapeutic markers for cell surface receptors, we performed exome sequencing (16 new samples, 22 previously published samples, total 38 with 26 matched normal DNA samples), RNA deep sequencing (17 new samples, 11 previously published samples, total 28 with 18 matched normal RNA samples), and immunohistochemistry (17 DIPG tissue samples) to examine the expression of the interleukin-4 (IL-4) signaling axis components (IL-4, interleukin 13 (IL-13), and their respective receptors IL-4Rα, IL-13Rα1, and IL-13Rα2). In addition, we correlated cytokine and receptor expression with expression of the oncogenes EGFR and c-MET. In DIPG tissues, transcript-level analysis found significant expression of IL-4, IL-13, and IL-13Rα1/2, with strong differential expression of IL-13Rα1/2 in tumor versus normal brain. At the protein level, immunohistochemical studies revealed high content of IL-4 and IL-13Rα1/2 but notably low expression of IL-13. Additionally, a strong positive correlation was observed between c-Met and IL-4Rα. The genomic and transcriptional landscape across all samples was also summarized. These data create a foundation for the design of potential new immunotherapies targeting IL-13 cell surface receptors in DIPG.
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spelling doaj.art-e0b9df0d759c44b28069717058dcfed62022-12-22T01:39:52ZengPublic Library of Science (PLoS)PLoS ONE1932-62032018-01-01134e019356510.1371/journal.pone.0193565IL-13 receptors as possible therapeutic targets in diffuse intrinsic pontine glioma.Noah E BerlowMatthew N SvalinaMichael J QuistTeagan P SettelmeyerViktor ZherebitskiyMari KogisoLin QiYuchen DuCynthia E HawkinsEsther HullemanXiao-Nan LiSakir H GultekinCharles KellerDiffuse intrinsic pontine glioma (DIPG) is a universally fatal childhood cancer of the brain. Despite the introduction of conventional chemotherapy and radiotherapy, improvements in survival have been marginal and long-term survivorship is uncommon. Thus, new targets for therapeutics are critically needed. Early phase clinical trials exploring molecularly-targeted therapies against the epidermal growth factor receptor (EGFR) and novel immunotherapies targeting interleukin receptor-13α2 (IL-13Rα2) have demonstrated activity in this disease. To identify additional therapeutic markers for cell surface receptors, we performed exome sequencing (16 new samples, 22 previously published samples, total 38 with 26 matched normal DNA samples), RNA deep sequencing (17 new samples, 11 previously published samples, total 28 with 18 matched normal RNA samples), and immunohistochemistry (17 DIPG tissue samples) to examine the expression of the interleukin-4 (IL-4) signaling axis components (IL-4, interleukin 13 (IL-13), and their respective receptors IL-4Rα, IL-13Rα1, and IL-13Rα2). In addition, we correlated cytokine and receptor expression with expression of the oncogenes EGFR and c-MET. In DIPG tissues, transcript-level analysis found significant expression of IL-4, IL-13, and IL-13Rα1/2, with strong differential expression of IL-13Rα1/2 in tumor versus normal brain. At the protein level, immunohistochemical studies revealed high content of IL-4 and IL-13Rα1/2 but notably low expression of IL-13. Additionally, a strong positive correlation was observed between c-Met and IL-4Rα. The genomic and transcriptional landscape across all samples was also summarized. These data create a foundation for the design of potential new immunotherapies targeting IL-13 cell surface receptors in DIPG.http://europepmc.org/articles/PMC5886401?pdf=render
spellingShingle Noah E Berlow
Matthew N Svalina
Michael J Quist
Teagan P Settelmeyer
Viktor Zherebitskiy
Mari Kogiso
Lin Qi
Yuchen Du
Cynthia E Hawkins
Esther Hulleman
Xiao-Nan Li
Sakir H Gultekin
Charles Keller
IL-13 receptors as possible therapeutic targets in diffuse intrinsic pontine glioma.
PLoS ONE
title IL-13 receptors as possible therapeutic targets in diffuse intrinsic pontine glioma.
title_full IL-13 receptors as possible therapeutic targets in diffuse intrinsic pontine glioma.
title_fullStr IL-13 receptors as possible therapeutic targets in diffuse intrinsic pontine glioma.
title_full_unstemmed IL-13 receptors as possible therapeutic targets in diffuse intrinsic pontine glioma.
title_short IL-13 receptors as possible therapeutic targets in diffuse intrinsic pontine glioma.
title_sort il 13 receptors as possible therapeutic targets in diffuse intrinsic pontine glioma
url http://europepmc.org/articles/PMC5886401?pdf=render
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