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• W4283029780 startingPage "1385" @default.
• W4283029780 abstract "Abstract Breast cancer (BC) remains the most common cancer, as well as the leading cause of cancer mortality in women worldwide [1]. Approximately 30% of patients with early-stage BC experience metastasis or a recurrent form of the disease [2]. The phenomenon of BC dormancy, where metastasised cancer cells remain in a quiescent phase at their disseminated location and for unknown reasons can become actively proliferative again, further adds to BC’s clinical burden with treatment at this secondary stage typically proving futile. An emerging avenue of research focuses on the metabolic properties of dormant BC cells (BCCs) and potential metabolic changes causing BCCs to enter/exit their quiescent state. Here we explore several studies that have uncovered changes in carbon metabolism underlying a dormant state, with conflicting studies uncovering shifts towards both glycolysis and/or oxidative phosphorylation. This review highlights that the metabolic states/shifts of dormant BCCs seem to be dependent on different BC subtypes and receptor status; however, more work needs to be done to fully map these differences. Building on the research that this review outlines could provide new personalised therapeutic possibilities for BC patients." @default.
• W4283029780 created "2022-06-18" @default.
• W4283029780 creator A5035201068 @default.
• W4283029780 creator A5040106108 @default.
• W4283029780 date "2022-06-17" @default.
• W4283029780 modified "2023-10-07" @default.
• W4283029780 title "Recent insights into the effects of metabolism on breast cancer cell dormancy" @default.
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• W4283029780 doi "https://doi.org/10.1038/s41416-022-01869-5" @default.
• W4283029780 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/35715635" @default.
• W4283029780 hasPublicationYear "2022" @default.
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