| Literature DB >> 34014536 |
Jessica Tan1, Anne Le2,3.
Abstract
Despite advances in screening, therapy, and surveillance that have improved patient survival rates, breast cancer is still the most commonly diagnosed cancer and the second leading cause of cancer mortality among women [1]. Breast cancer is a highly heterogeneous disease rooted in a genetic basis, influenced by extrinsic stimuli, and reflected in clinical behavior. The diversity of breast cancer hormone receptor status and the expression of surface molecules have guided therapy decisions for decades; however, subtype-specific treatment often yields diverse responses due to varying tumor evolution and malignant potential. Although the mechanisms behind breast cancer heterogeneity is not well understood, available evidence suggests that studying breast cancer metabolism has the potential to provide valuable insights into the causes of these variations as well as viable targets for intervention.Entities:
Keywords: Breast cancer; Choline metabolism; Estrogen metabolism; Estrogen receptor status; Glycolytic upregulation; Intratumoral heterogeneity; Metabolic adaptivity; Metabolic fingerprint; Serine biosynthesis
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Year: 2021 PMID: 34014536 DOI: 10.1007/978-3-030-65768-0_6
Source DB: PubMed Journal: Adv Exp Med Biol ISSN: 0065-2598 Impact factor: 2.622