Comparative biological activity of palbociclib and ribociclib in hormone receptor-positive breast cancer
Details
Publication Year 2024-07-11,Volume 14,Issue #1,Page 16030
Journal Title
Scientific Reports
Publication Type
Research article
Abstract
This study examines the biological effects of palbociclib and ribociclib in hormone receptor-positive breast cancer, pivotal to the HARMONIA prospective phase III clinical trial. We explore the downstream impacts of these CDK4/6 inhibitors, focusing on cell lines and patient-derived tumor samples. We treated HR+ breast cancer cell lines (T47D, MCF7, and BT474) with palbociclib or ribociclib (100 nM or 500 nM), alone or combined with fulvestrant (1 nM), over periods of 24, 72, or 144 h. Our assessments included PAM50 gene expression, RB1 phosphorylation, Lamin-B1 protein levels, and senescence-associated β-galactosidase activity. We further analyzed PAM50 gene signatures from the CORALLEEN and NeoPalAna phase II trials. Both CDK4/6 inhibitors similarly inhibited proliferation across the cell lines. At 100 nM, both drugs partially reduced p-RB1, with further decreases at 500 nM over 144 h. Treatment led to reduced Lamin-B1 expression and increased senescence-associated β-galactosidase activity. Both drugs enhanced Luminal A and reduced Luminal B and proliferation signatures at both doses. However, the HER2-enriched signature significantly diminished only at the higher dose of 500 nM. Corresponding changes were observed in tumor samples from the CORALLEEN and NeoPalAna studies. At 2 weeks of treatment, both drugs significantly reduced the HER2-enriched signature, but at surgery, this reduction was consistent only with ribociclib. Our findings suggest that while both CDK4/6 inhibitors effectively modulate key biological pathways in HR+/HER2- breast cancer, nuances in their impact, particularly on the HER2-enriched signature, are dose-dependent, influenced by the addition of fulvestrant and warrant further investigation.
Publisher
Springer Nature
Keywords
Humans; *Aminopyridines/pharmacology; *Piperazines/pharmacology; *Purines/pharmacology; *Pyridines/pharmacology; *Breast Neoplasms/drug therapy/metabolism/pathology; Female; *Cell Proliferation/drug effects; Cell Line, Tumor; Receptors, Estrogen/metabolism; Fulvestrant/pharmacology; Receptor, ErbB-2/metabolism/genetics; Cyclin-Dependent Kinase 4/metabolism; Receptors, Progesterone/metabolism; Protein Kinase Inhibitors/pharmacology; Cyclin-Dependent Kinase 6/metabolism; Gene Expression Regulation, Neoplastic/drug effects
Department(s)
Laboratory Research
Open Access at Publisher's Site
https://doi.org/10.1038/s41598-024-67126-2
Terms of Use/Rights Notice
Refer to copyright notice on published article.


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