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Naslov:Comprehensive molecular characterization of craniopharyngiomas using whole transcriptome and spatial transcriptomics approaches
Avtorji:ID Kert, Špela (Avtor)
ID Matjašič, Alenka (Avtor)
ID Pižem, Jože (Avtor)
ID Mlakar, Jernej (Avtor)
ID Bošnjak, Matic (Avtor)
ID Jerala, Miha (Avtor)
ID Kotnik, Primož (Avtor)
ID Faganel Kotnik, Barbara (Avtor)
ID Kitanovski, Lidija (Avtor)
ID Zupan, Andrej (Avtor)
Datoteke:.pdf PDF - Predstavitvena datoteka, prenos (2,18 MB)
MD5: 1FB57E981DF59B6F3761B7A1F5A8A18E
 
URL URL - Izvorni URL, za dostop obiščite https://link.springer.com/article/10.1007/s10014-025-00509-z
 
Jezik:Angleški jezik
Tipologija:1.01 - Izvirni znanstveni članek
Organizacija:Logo UKC LJ - Univerzitetni klinični center Ljubljana
Povzetek:Craniopharyngiomas (CPs) are rare benign brain tumors that are classified as WHO grade I, with two subtypes: adamantinomatous craniopharyngioma (ACP) and papillary craniopharyngioma (PCP). ACP is caused by somatic mutations in exon 3 of the CTNNB1 gene activating the Wnt signaling pathway. PCP is associated with somatic BRAF p.V600E mutations activating the MAPK signaling pathway. Understanding their molecular differences is crucial for diagnosis and treatment. This study aimed to analyze common somatic alterations in ACP and PCP using bulk transcriptome sequencing and in situ spatial transcriptomics. RNA sequencing and high-resolution spatial profiling were used to detect mutations and examine gene expression differences among ACP, PCP, and healthy pituitary tissue. Whole transcriptome sequencing was performed on 24 tumor samples, with healthy pituitary data from the GTEx portal. Bioinformatics analysis utilized the CTAT mutation pipeline, with Sanger sequencing for validation. Results confirmed BRAF p.V600E mutations in all PCP samples and CTNNB1 mutations in all ACP samples. Differential gene expression analysis highlighted distinct molecular profiles and reinforced the involvement of Wnt and MAPK signaling. Spatial profiling identified 41 differentially expressed genes between ACP and PCP. This study provides critical insights into CP biology, supporting improved diagnostics and potential therapeutic strategies.
Ključne besede:craniopharyngioma, differential gene expression, in situ spatial profiling, somatic mutation detection, transcriptional analysis
Status publikacije:Objavljeno
Verzija publikacije:Objavljena publikacija
Leto izida:2025
Št. strani:str. 130–142
Številčenje:Vol. 42, issue 4
PID:20.500.12556/DiRROS-28869 Novo okno
UDK:61
ISSN pri članku:1433-7398
DOI:10.1007/s10014-025-00509-z Novo okno
COBISS.SI-ID:243867907 Novo okno
Opomba:
Datum objave v DiRROS:10.04.2026
Število ogledov:106
Število prenosov:64
Metapodatki:XML DC-XML DC-RDF
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Gradivo je del revije

Naslov:Brain tumor pathology
Skrajšan naslov:Brain tumor pathol.
Založnik:Springer.
ISSN:1433-7398
COBISS.SI-ID:514824217 Novo okno

Gradivo je financirano iz projekta

Financer:ARIS - Javna agencija za znanstvenoraziskovalno in inovacijsko dejavnost Republike Slovenije
Številka projekta:P3-0054-2020
Naslov:Patologija in molekularna genetika

Licence

Licenca:CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.

Sekundarni jezik

Jezik:Slovenski jezik
Ključne besede:kraniofaringiom, diferencialna genska ekspresija, prostorsko profiliranje in situ, odkrivanje somatskih mutacij, transkripcijska analiza


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