| Literature DB >> 33809117 |
Smarakan Sneha1, Simon C Baker2, Andrew Green3, Sarah Storr3, Radhika Aiyappa3, Stewart Martin3, Klaus Pors1.
Abstract
Despite significant advances in treatment strategies over the past decade, selective treatment of breast cancer with limited side-effects still remains a great challenge. The cytochrome P450 (CYP) family of enzymes contribute to cancer cell proliferation, cell signaling and drug metabolism with implications for treatment outcomes. A clearer understanding of CYP expression is important in the pathogenesis of breast cancer as several isoforms play critical roles in metabolising steroid hormones and xenobiotics that contribute to the genesis of breast cancer. The purpose of this review is to provide an update on how the presence of CYPs impacts on standard of care (SoC) drugs used to treat breast cancer as well as discuss opportunities to exploit CYP expression for therapeutic intervention. Finally, we provide our thoughts on future work in CYP research with the aim of supporting ongoing efforts to develop drugs with improved therapeutic index for patient benefit.Entities:
Keywords: AQ4N; CYP1A1; CYP1B1; CYP2W1; Cytochrome P450; bioprecursor; breast cancer; duocarmycin; phortress; prodrug
Year: 2021 PMID: 33809117 PMCID: PMC7998590 DOI: 10.3390/biomedicines9030290
Source DB: PubMed Journal: Biomedicines ISSN: 2227-9059