Abstract
Cyclin D1 is downstream of erbB2 and is required for erbB2 transformation. Here we report thatcyclin D1 functions are essential, rate limiting for erbB2 transformation, and reciprocally increase erbB2 levels. This interaction depends on three cyclin D1 activities: cyclin-dependent kinase 4-dependent kinase activity, titration of p27, and an intrinsic transcriptional activity of cyclin D1. Drugs active against erbB2 and cyclin D1 (Herceptin and flavopiridol) were synergistically cytotoxic against erbB2-positive breast cancer cell lines. Addition of flavopiridol to Herceptin synergistically lowered erbB2 levels in these cells. Our data suggest the potential use of combinations of cyclin-dependent kinase inhibitors and Herceptin in breast cancer.
Publication types
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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3T3 Cells
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Animals
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Antibodies, Monoclonal / administration & dosage
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Antibodies, Monoclonal / pharmacology*
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Antibodies, Monoclonal, Humanized
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Antineoplastic Combined Chemotherapy Protocols / pharmacology*
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Breast Neoplasms / drug therapy
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Breast Neoplasms / metabolism
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Cell Survival / drug effects
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Cell Transformation, Neoplastic / drug effects
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Cell Transformation, Neoplastic / metabolism*
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Cyclin D1 / antagonists & inhibitors
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Cyclin D1 / metabolism
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Cyclin D1 / physiology*
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Cyclin-Dependent Kinase 4
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Cyclin-Dependent Kinases / antagonists & inhibitors
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Cyclin-Dependent Kinases / metabolism
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Drug Synergism
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Flavonoids / administration & dosage
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Flavonoids / pharmacology*
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Humans
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Mice
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Piperidines / administration & dosage
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Piperidines / pharmacology*
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Proto-Oncogene Proteins*
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Receptor, ErbB-2 / genetics
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Receptor, ErbB-2 / metabolism
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Receptor, ErbB-2 / physiology*
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Trastuzumab
Substances
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Antibodies, Monoclonal
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Antibodies, Monoclonal, Humanized
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Flavonoids
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Piperidines
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Proto-Oncogene Proteins
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Cyclin D1
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alvocidib
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Receptor, ErbB-2
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CDK4 protein, human
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Cdk4 protein, mouse
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Cyclin-Dependent Kinase 4
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Cyclin-Dependent Kinases
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Trastuzumab