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Rethinking Our Approach to Cancer Metabolism to Deliver Patient Benefit

Overview
Journal Br J Cancer
Specialty Oncology
Date 2023 Jun 20
PMID 37340094
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Abstract

Altered cellular metabolism is a major mechanism by which tumours support nutrient consumption associated with increased cellular proliferation. Selective dependency on specific metabolic pathways provides a therapeutic vulnerability that can be targeted in cancer therapy. Anti-metabolites have been used clinically since the 1940s and several agents targeting nucleotide metabolism are now well established as standard of care treatment in a range of indications. However, despite great progress in our understanding of the metabolic requirements of cancer and non-cancer cells within the tumour microenvironment, there has been limited clinical success for novel agents targeting pathways outside of nucleotide metabolism. We believe that there is significant therapeutic potential in targeting metabolic processes within cancer that is yet to be fully realised. However, current approaches to identify novel targets, test novel therapies and select patient populations most likely to benefit are sub-optimal. We highlight recent advances in technologies and understanding that will support the identification and validation of novel targets, re-evaluation of existing targets and design of optimal clinical positioning strategies to deliver patient benefit.

Citing Articles

Site of breast cancer metastasis is independent of single nutrient levels.

Abbott K, Subudhi S, Ferreira R, Gultekin Y, Steinbuch S, Munim M bioRxiv. 2024; .

PMID: 39484531 PMC: 11527034. DOI: 10.1101/2024.10.24.616714.

References
1.
St John E, Balog J, McKenzie J, Rossi M, Covington A, Muirhead L . Rapid evaporative ionisation mass spectrometry of electrosurgical vapours for the identification of breast pathology: towards an intelligent knife for breast cancer surgery. Breast Cancer Res. 2017; 19(1):59. PMC: 5442854. DOI: 10.1186/s13058-017-0845-2. View

2.
Johnson J, Decker S, Zaharevitz D, Rubinstein L, Venditti J, SCHEPARTZ S . Relationships between drug activity in NCI preclinical in vitro and in vivo models and early clinical trials. Br J Cancer. 2001; 84(10):1424-31. PMC: 2363645. DOI: 10.1054/bjoc.2001.1796. View

3.
Leney-Greene M, Boddapati A, Su H, Cantor J, Lenardo M . Human Plasma-like Medium Improves T Lymphocyte Activation. iScience. 2019; 23(1):100759. PMC: 6941860. DOI: 10.1016/j.isci.2019.100759. View

4.
Xu J, Yu T, Zois C, Cheng J, Tang Y, Harris A . Unveiling Cancer Metabolism through Spontaneous and Coherent Raman Spectroscopy and Stable Isotope Probing. Cancers (Basel). 2021; 13(7). PMC: 8038603. DOI: 10.3390/cancers13071718. View

5.
Najumudeen A, Ceteci F, Fey S, Hamm G, Steven R, Hall H . The amino acid transporter SLC7A5 is required for efficient growth of KRAS-mutant colorectal cancer. Nat Genet. 2021; 53(1):16-26. DOI: 10.1038/s41588-020-00753-3. View