SMARCB1 Deficiency as a Driver of the Hallmarks of Cancer in Rhabdoid Tumours: Novel Insights into Dysregulated Energy Metabolism, Emerging Targets, and Ongoing Clinical Trials
<b>Background:</b> Rhabdoid tumours (RTs) are aggressive neoplasms most often characterised by biallelic loss of the SMARCB1 gene, encoding a core subunit of the SWI/SNF chromatin-remodelling complex. Despite their relative genetic stability, RTs exhibit a highly malignant phenotype and...
Saved in:
| Main Authors: | Abdul L. Shakerdi, Graham P. Pidgeon |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
MDPI AG
2025-05-01
|
| Series: | Metabolites |
| Subjects: | |
| Online Access: | https://www.mdpi.com/2218-1989/15/5/304 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
SMARCB1- and vimentin-positive esophageal carcinoma with undifferentiated components, rhabdoid features, and a good prognosis: a case report
by: Hideki Nagano, et al.
Published: (2019-01-01) -
Case report: administration of immune checkpoint inhibitor for SMARCB1 (INI1)-negative rhabdoid carcinoma with microsatellite instability (MSI)-high in the right colon
by: Toshinori Kobayashi, et al.
Published: (2023-02-01) -
The rhabdoid variant of adrenocortical carcinoma-Report of three cases and literature review
by: Pavithra Ayyanar, et al.
Published: (2023-07-01) -
Aggressive CNS Embryonal Tumours: A Series of Three Cases
by: Shima Kannadas, et al.
Published: (2025-07-01) -
Concurrent Cutaneous and Retropharyngeal Rhabdoid Tumors in a Female Infant: A Rare Case Report and a Review of the Literature
by: Mohammad Dabour Asad, et al.