Is System x c - a Suitable Target for Tumour Detection and Response Assessment with Imaging?

Autor: Sharkey AR; School of Biomedical Engineering and Imaging Sciences, King's College London, St. Thomas' Hospital, London SE1 7EH, UK., Witney TH; School of Biomedical Engineering and Imaging Sciences, King's College London, St. Thomas' Hospital, London SE1 7EH, UK., Cook GJR; School of Biomedical Engineering and Imaging Sciences, King's College London, St. Thomas' Hospital, London SE1 7EH, UK.; King's College London and Guy's and St. Thomas' PET Centre, St. Thomas' Hospital, London SE1 7EH, UK.
Jazyk: angličtina
Zdroj: Cancers [Cancers (Basel)] 2023 Nov 24; Vol. 15 (23). Date of Electronic Publication: 2023 Nov 24.
DOI: 10.3390/cancers15235573
Abstrakt: System x c - is upregulated in cancer cells and can be imaged using novel radiotracers, most commonly with (4S)-4-(3-[ 18 F]fluoropropyl)-L-glutamic acid ( 18 F-FSPG). The aim of this review was to summarise the use of 18 F-FSPG in humans, explore the benefits and limitations of 18 F-FSPG, and assess the potential for further use of 18 F-FSPG in cancer patients. To date, ten papers have described the use of 18 F-FSPG in human cancers. These studies involved small numbers of patients (range 1-26) and assessed the use of 18 F-FSPG as a general oncological diagnostic agent across different cancer types. These clinical trials were contrasting in their findings, limiting the scope of 18 F-FSPG PET/CT as a purely diagnostic agent, primarily due to heterogeneity of 18 F-FSPG retention both between cancer types and patients. Despite these limitations, a potential further application for 18 F-FSPG is in the assessment of early treatment response and prediction of treatment resistance. Animal models of cancer have shown that changes in 18 F-FSPG retention following effective therapy precede glycolytic changes, as indicated by 18 F-FDG, and changes in tumour volume, as measured by CT. If these results could be replicated in human clinical trials, imaging with 18 F-FSPG PET/CT would offer an exciting route towards addressing the currently unmet clinical needs of treatment resistance prediction and early imaging assessment of therapy response.
Competing Interests: The authors declare no conflicts of interest.
Databáze: MEDLINE
Externí odkaz:
Nepřihlášeným uživatelům se plný text nezobrazuje