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Biological Effects of Cyclin-Dependent Kinase Inhibitors Ribociclib,Palbociclib and Abemaciclib on Breast Cancer Bone Microenvironment
Authors:Michele Iuliani  Sonia Simonetti  Giulia Ribelli  Andrea Napolitano  Umile Giuseppe Longo  Bruno Vincenzi  Paolo Orsaria  Vincenzo Denaro  Giuseppe Tonini  Daniele Santini  Pantano Francesco
Affiliation:1.Department of Medical Oncology, Campus Bio-Medico University of Rome, 00128 Rome, Italy; (S.S.); (G.R.); (A.N.); (B.V.); (G.T.); (D.S.); (P.F.);2.Royal Marsden Hospital NHS Trust, London SW3 6JJ, UK;3.Department of Orthopedic and Trauma Surgery, Campus Bio-Medico University of Rome, 00128 Rome, Italy; (U.G.L.); (V.D.);4.Department of Breast Surgery, Campus Bio-Medico University Hospital of Rome, 00128 Rome, Italy;
Abstract:The CDK4/6 inhibitors (CDKi) palbociclib, ribociclib, and abemaciclib are currently approved in combination with anti-estrogen therapy for the treatment of advanced and/or metastatic hormone receptor-positive/HER2-neu-negative breast cancer patients. Given the high incidence of bone metastases in this population, we investigated and compared the potential effects of palbociclib, ribociclib, and abemaciclib on the breast cancer bone microenvironment. Primary osteoclasts (OCs) and osteoblasts (OBs) were obtained from human monocyte and mesenchymal stem cells, respectively. OC function was evaluated by tartrate-resistant acid phosphatase assay and real-time PCR; OB activity was assessed by an alizarin red assay. OB/breast cancer co-culture models were generated via the seeding of MCF-7 cells on a layer of OBs, and tumor cell proliferation was analyzed using flow cytometry. Here, we showed that ribociclib, palbociclib, and abemaciclib exerted similar inhibitory effects on the OC differentiation and expression of bone resorption markers without affecting OC viability. On the other hand, the three CDKi did not affect the ability of OB to produce bone matrix, even if the higher doses of palbociclib and abemaciclib reduced the OB viability. In OB/MCF-7 co-culture models, palbociclib demonstrated a lower anti-tumor effect than ribociclib and abemaciclib. Overall, our results revealed the direct effects of CDKi on the tumor bone microenvironment, highlighting differences potentially relevant for clinical practice.
Keywords:CDK4/6 inhibitors  breast cancer  bone tumor microenvironment  osteoclasts  osteoblasts
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