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DIPG-48. DIPG THROUGH THE LOOKING GLASS

Diffuse intrinsic pontine glioma (DIPG) has a peculiar pathogenesis with canonical Histone variants H3.1/H3.2 wherein Lysine 27 (H3K27) is substituted to methionine (H3K27M). It is restricted to pons and affects young children whereas non canonical H3.3 mutations result in tumours across the midline...

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Autor principal: Senga, Sasi S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10260040/
http://dx.doi.org/10.1093/neuonc/noad073.095
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author Senga, Sasi S
author_facet Senga, Sasi S
author_sort Senga, Sasi S
collection PubMed
description Diffuse intrinsic pontine glioma (DIPG) has a peculiar pathogenesis with canonical Histone variants H3.1/H3.2 wherein Lysine 27 (H3K27) is substituted to methionine (H3K27M). It is restricted to pons and affects young children whereas non canonical H3.3 mutations result in tumours across the midline and affects older children. This discrepancy in the spatiotemporal distribution provides cues to target DIPG. Based on altered neuronal signalling which is a hallmark of cancer, a deeper understanding of neuron tumour interaction may unravel numerous new targets. One such target is light. The restriction of specific spectrum of light may hinder the progression and even the development of tumours in young children. It provides a lucrative therapeutic option which can be implemented merely by blocking a certain spectrum of light with glasses in an otherwise baffling disease. It warrants a deeper understanding of the light exposure on DIPG tumour progression.
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spelling pubmed-102600402023-06-13 DIPG-48. DIPG THROUGH THE LOOKING GLASS Senga, Sasi S Neuro Oncol Final Category: Diffuse Intrinsic Pontine Glioma/Diffuse Midline Gliomas - DPIG Diffuse intrinsic pontine glioma (DIPG) has a peculiar pathogenesis with canonical Histone variants H3.1/H3.2 wherein Lysine 27 (H3K27) is substituted to methionine (H3K27M). It is restricted to pons and affects young children whereas non canonical H3.3 mutations result in tumours across the midline and affects older children. This discrepancy in the spatiotemporal distribution provides cues to target DIPG. Based on altered neuronal signalling which is a hallmark of cancer, a deeper understanding of neuron tumour interaction may unravel numerous new targets. One such target is light. The restriction of specific spectrum of light may hinder the progression and even the development of tumours in young children. It provides a lucrative therapeutic option which can be implemented merely by blocking a certain spectrum of light with glasses in an otherwise baffling disease. It warrants a deeper understanding of the light exposure on DIPG tumour progression. Oxford University Press 2023-06-12 /pmc/articles/PMC10260040/ http://dx.doi.org/10.1093/neuonc/noad073.095 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Final Category: Diffuse Intrinsic Pontine Glioma/Diffuse Midline Gliomas - DPIG
Senga, Sasi S
DIPG-48. DIPG THROUGH THE LOOKING GLASS
title DIPG-48. DIPG THROUGH THE LOOKING GLASS
title_full DIPG-48. DIPG THROUGH THE LOOKING GLASS
title_fullStr DIPG-48. DIPG THROUGH THE LOOKING GLASS
title_full_unstemmed DIPG-48. DIPG THROUGH THE LOOKING GLASS
title_short DIPG-48. DIPG THROUGH THE LOOKING GLASS
title_sort dipg-48. dipg through the looking glass
topic Final Category: Diffuse Intrinsic Pontine Glioma/Diffuse Midline Gliomas - DPIG
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10260040/
http://dx.doi.org/10.1093/neuonc/noad073.095
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