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A noncanonical function of the tyrosine degradation enzyme FAH drives CDK4/6 inhibitor resistance in breast cancer.

Jenny Högström, Hanna M Doh, Aidan Kump, Boryana Petrova, Peng Wang, Jonathan D Lee, Kaisa Koivula, Nina Kozlova, Kayla A Cruz, Su Min Hong, Camila Perea, Arjun Garg, Michal Weitman, Conor L Evans, Jonathan L Coloff, Jaymin M Patel, Gerburg M Wulf, Laura C Collins, Naama Kanarek, Taru Muranen

Science advancesOct 2, 2026PMID 42814811doi:10.1126/sciadv.aef1145 Journal ArticlepubmedProvenance
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PubMed
Retrieved
Oct 1, 2026
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normalized (units and labels harmonized; values unchanged)
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ING-PUBMED-20261001-000001
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Resistance to standard-of-care therapies remains a major clinical challenge in the treatment of the most common breast cancer, the hormone receptor-positive (HR+) subtype. Cyclin-dependent kinase 4/6 (CDK4/6) inhibitors improve outcomes in early-stage HR+ disease, yet many patients relapse.…

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