Extracellular histones profiles of pediatric H3K27-altered diffuse midline glioma
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00159816%3A_____%2F25%3A00081673" target="_blank" >RIV/00159816:_____/25:00081673 - isvavai.cz</a>
Výsledek na webu
<a href="https://link.springer.com/article/10.1007/s40291-024-00754-6" target="_blank" >https://link.springer.com/article/10.1007/s40291-024-00754-6</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1007/s40291-024-00754-6" target="_blank" >10.1007/s40291-024-00754-6</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Extracellular histones profiles of pediatric H3K27-altered diffuse midline glioma
Popis výsledku v původním jazyce
yocardial deformation imaging is a very attractive clinical tool for the assessment of right ventricular (RV) systolic performance, providing incremental diagnostic and prognostic information over the traditional indices of RV function. Among various imaging modalities, echocardiography is currently the Diffuse midline glioma, H3 K27-altered (DMG) is a fatal tumour that arises in the midline structures of the brain. When located in the pons, it is more commonly referred to as diffuse intrinsic pontine glioma (DIPG). DMG/DIPG is usually diagnosed when children are < 10 years, and it has a median overall survival of < 12 months after diagnosis. Radiological imaging is still the gold standard for DIPG diagnosis while the use of biopsy procedures led to our knowledge on its biology, such as with the identification of the canonical histone H3K27M mutation. However, the need to improve survival encourages the development of non-invasive, fast and inexpensive assays on biofluids for optimizing molecular diagnoses in DMG/DIPG. Here, we propose a rapid, new, imaging and epigenetics-based approach to diagnose DMG/DIPG in the plasma of paediatric patients.
Název v anglickém jazyce
Extracellular histones profiles of pediatric H3K27-altered diffuse midline glioma
Popis výsledku anglicky
yocardial deformation imaging is a very attractive clinical tool for the assessment of right ventricular (RV) systolic performance, providing incremental diagnostic and prognostic information over the traditional indices of RV function. Among various imaging modalities, echocardiography is currently the Diffuse midline glioma, H3 K27-altered (DMG) is a fatal tumour that arises in the midline structures of the brain. When located in the pons, it is more commonly referred to as diffuse intrinsic pontine glioma (DIPG). DMG/DIPG is usually diagnosed when children are < 10 years, and it has a median overall survival of < 12 months after diagnosis. Radiological imaging is still the gold standard for DIPG diagnosis while the use of biopsy procedures led to our knowledge on its biology, such as with the identification of the canonical histone H3K27M mutation. However, the need to improve survival encourages the development of non-invasive, fast and inexpensive assays on biofluids for optimizing molecular diagnoses in DMG/DIPG. Here, we propose a rapid, new, imaging and epigenetics-based approach to diagnose DMG/DIPG in the plasma of paediatric patients.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
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OECD FORD obor
30300 - Health sciences
Návaznosti výsledku
Projekt
<a href="/cs/project/NU23-03-00318" target="_blank" >NU23-03-00318: Volně cirkulující histonové komplexy jako diagnostický nástroj dětských nádorových onemocnění centrálního nervového systému (CNS).</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Ostatní
Rok uplatnění
2025
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Molecular diagnosis and therapy
ISSN
1177-1062
e-ISSN
1179-2000
Svazek periodika
29
Číslo periodika v rámci svazku
1
Stát vydavatele periodika
NZ - Nový Zéland
Počet stran výsledku
13
Strana od-do
129-141
Kód UT WoS článku
001351167600002
EID výsledku v databázi Scopus
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