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Probing intratumoral metabolic compartmentalisation in a patient with fumarate hydratase-deficient renal cancer using clinical hyperpolarised 13C-MRI and mass spectrometry imaging.

Title: Probing intratumoral metabolic compartmentalisation in a patient with fumarate hydratase-deficient renal cancer using clinical hyperpolarised 13C-MRI and mass spectrometry imaging.
Authors: Horvat-Menih, Ines; Casey, Ruth; Denholm, James; Hamm, Gregory; Hulme, Heather; Gallon, John; Khan, Alixander S; Kaggie, Joshua; Gill, Andrew B; Priest, Andrew N; Duarte, Joao AG; Yong, Cissy; Brodie, Cara; Whitworth, James; Barry, Simon T; Goodwin, Richard JA; Anand, Shubha; Dodd, Marc; Honan, Katherine; Welsh, Sarah J; Warren, Anne Y; Aho, Tevita; Stewart, Grant D; Mitchell, Thomas J; McLean, Mary A; Gallagher, Ferdia A
Publisher Information: Springer Nature; Department of Radiology; //doi.org/10.1038/s43856-025-01371-y
Publication Year: 2026
Collection: Apollo - University of Cambridge Repository
Subject Terms: 32 Biomedical and Clinical Sciences; 3211 Oncology and Carcinogenesis; Health Disparities and Racial or Ethnic Minority Health Research; Clinical Research; Health Disparities; Cancer; Biomedical Imaging; Rare Diseases; Kidney Disease; 2.1 Biological and endogenous factors; 4.2 Evaluation of markers and technologies; 4.4 Population screening
Description: BACKGROUND: Fumarate hydratase-deficient renal cell carcinoma (FHd-RCC) is a rare and aggressive renal cancer subtype characterised by increased fumarate accumulation and upregulated lactate production. Renal tumours demonstrate significant intratumoral metabolic heterogeneity, which may contribute to treatment failure. Emerging non-invasive metabolic imaging techniques have clinical potential to more accurately phenotype tumour metabolism and its heterogeneity. METHODS: In this case study we have used hyperpolarised 13C-pyruvate MRI (HP 13C-MRI) to assess 13C-lactate generation in a patient with an organ-confined FHd-RCC. Post-operative tissue samples were co-registered with imaging and underwent sequencing, IHC staining, and mass spectrometry imaging (MSI). RESULTS: HP 13C-MRI reveals two metabolically distinct tumour regions. The 13C-lactate-rich region shows a high lactate/pyruvate ratio and slightly lower fumarate on MSI compared to the other tumour region, as well as increased CD8 + T cell infiltration, and genetic dedifferentiation. Compared to the normal kidney, the vascularity in the tumour is decreased, while immune cell fraction is markedly higher. CONCLUSIONS: This study shows the potential of metabolic HP 13C-MRI to characterise FHd-RCC and how targeting of biopsies to regions of metabolic dysregulation could be used to obtain the tumour samples of greatest clinical significance, which in turn can inform on early and successful response to treatment.
Document Type: article in journal/newspaper
File Description: Print-Electronic; application/pdf
Language: English
Relation: https://www.repository.cam.ac.uk/handle/1810/395787; https://doi.org/10.17863/CAM.125187
DOI: 10.17863/CAM.125187
Availability: https://www.repository.cam.ac.uk/handle/1810/395787; https://doi.org/10.17863/CAM.125187
Rights: Attribution 4.0 International ; https://creativecommons.org/licenses/by/4.0/
Accession Number: edsbas.B2052204
Database: BASE