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Dexamethasone down-regulates ABCG2 expression levels in breast cancer cells
Authors:Honorat Mylène  Mesnier Aurélia  Di Pietro Attilio  Lin Valérie  Cohen Pascale  Dumontet Charles  Payen Léa
Institution:a Université de Lyon, Lyon1, Lyon, F-69008, France
b INSERM U590, Université Lyon 1, Laboratoire de cytologie analytique, Rockefeller, 8, Avenue Rockefeller, Lyon F-69008, France
c Centre Léon Bérard, FNCLCC, Lyon, F-69008, France
d IBCP, UMR 5086 CNRS, Université de Lyon, Lyon, F-69007, France
e School of Biological Sciences, Nanyang Technological University, Singapore
Abstract:The breast cancer resistance protein ABCG2 effluxes a variety of drugs and is believed to play an important role in multidrug resistance to chemotherapy. We show here for the first time that dexamethasone (DEX) and progesterone (PROG) are able to strongly inhibit ABCG2 expression in progesterone receptor (PR)-positive MCF7 and PR-negative MDA-MB-231 breast cells. In contrast, in the latter cells stably-transfected with progesterone receptor isoforms A and B, ABCG2 expression was strongly up-regulated by DEX and PROG. In addition, two other ligands of Pregnane X Receptor (PXR) and/or Glucocorticoid Receptor (GR) were also able to down-regulate ABCG2 expression in PXR- and GR-positive MCF7 cells. ABCG2 expression regulation by DEX likely resulted from the activation of PR-, PXR-, and/or GR-signaling pathways. ABCG2 expression inhibition by DEX was associated with increased sensitivity to mitoxantrone, a known ABCG2 substrate. The findings suggest that DEX may be useful in improving drug efficacy under certain conditions.
Keywords:ABC  ATP-Binding Cassette  BCRP/ABCG2  breast cancer resistance protein  CHX  cycloheximide  DEX  dexamethasone  E2  estrogen  GRE  glucocortocoid-response element  MIT  mitoxantrone  PCN  pregnenolone 16α-carbonitrile  PROG  progesterone  PR  progesterone receptor  PRA or PRB  progesterone receptor A or B  PRE  progesterone-response element  ERE  estrogen-response element  PXR  Pregnane X Receptor  QRT-PCR  quantitative real-time polymerase chain reaction
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