The CD44s Isoform is a Potential Biomarker for Predicting Craniopharyngioma Recurrence in Children.


Journal

Neuromolecular medicine
ISSN: 1559-1174
Titre abrégé: Neuromolecular Med
Pays: United States
ID NLM: 101135365

Informations de publication

Date de publication:
17 Jul 2024
Historique:
received: 06 06 2024
accepted: 04 07 2024
medline: 18 7 2024
pubmed: 18 7 2024
entrez: 17 7 2024
Statut: epublish

Résumé

Adamantinomatous craniopharyngioma (ACP) is an intracranial tumor considered partly malignant due to its ability to infiltrate surrounding structures and tendency to relapse despite radical resection. CD44 is a known stem cell marker in ACP and is upregulated in cell clusters of invasive ACP protrusions; however, the functions of its alternative splicing isoform variants, CD44s and CD44v1-10, have not yet been studied in terms of ACP recurrence, despite their confirmed roles in cancer development and progression. In this study, we first confirmed the difference in total CD44 expression between samples from patients who experienced relapse and those from patients who did not. Moreover, our findings showed that, in recurrent samples, the predominant isoform expressed was CD44s, which might indicate its significance in predicting ACP recurrence. The association between increased CD44 expression and recurrence may lead to the development of prognostic markers of ACP aggressiveness and relapse potential; however, further studies are needed to clarify the exact mechanism of CD44 expression.

Identifiants

pubmed: 39020106
doi: 10.1007/s12017-024-08797-y
pii: 10.1007/s12017-024-08797-y
doi:

Substances chimiques

Hyaluronan Receptors 0
Biomarkers, Tumor 0
CD44 protein, human 0
Protein Isoforms 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

30

Subventions

Organisme : Institutional grant of Medical University of Silesia
ID : KNW-1-202/N/8/O

Informations de copyright

© 2024. The Author(s).

Références

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Auteurs

K Bajdak-Rusinek (K)

Department of Medical Genetics, Faculty of Medical Sciences in Katowice, Medical University of Silesia, Medykow 18 Street, 40-752, Katowice, Poland. kbajdak-rusinek@sum.edu.pl.

N Diak (N)

Department of Medical Genetics, Faculty of Medical Sciences in Katowice, Medical University of Silesia, Medykow 18 Street, 40-752, Katowice, Poland.

E Gutmajster (E)

Biotechnology Centre, Silesian University of Technology, Gliwice, Poland.

A Fus-Kujawa (A)

Department of Medical Genetics, Faculty of Medical Sciences in Katowice, Medical University of Silesia, Medykow 18 Street, 40-752, Katowice, Poland.

M Ciupińska (M)

Department of Pathomorphology and Molecular Diagnostics, Medical University of Silesia, 40-752, Katowice, Poland.

B Kalina-Faska (B)

Department of Pediatrics and Pediatric Endocrinology, Faculty of Medical Science, Medical University of Silesia, Katowice, Poland.

A Trybus (A)

Department of Medical Genetics, Faculty of Medical Sciences in Katowice, Medical University of Silesia, Medykow 18 Street, 40-752, Katowice, Poland.
Students Scientific Society, Faculty of Medical Sciences in Katowice, Medical University of Silesia, Katowice, Poland.

M Grajek (M)

Center for Cardiovascular Research and Development, American Heart of Poland, 40-028, Katowice, Poland.

M Kalina (M)

Department of Medical Genetics, Faculty of Medical Sciences in Katowice, Medical University of Silesia, Medykow 18 Street, 40-752, Katowice, Poland.

M Mandera (M)

Department of Pediatric Neurosurgery, Medical University of Silesia, Katowice, Poland.

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