Breast cancer resistance protein exports sulfated estrogens but not free estrogens.

Article Details

Citation

Imai Y, Asada S, Tsukahara S, Ishikawa E, Tsuruo T, Sugimoto Y

Breast cancer resistance protein exports sulfated estrogens but not free estrogens.

Mol Pharmacol. 2003 Sep;64(3):610-8.

PubMed ID
12920197 [ View in PubMed
]
Abstract

Breast cancer resistance protein (BCRP), an ATP-binding cassette transporter, confers resistance to a series of anticancer reagents such as mitoxantrone, 7-ethyl-10-hydroxycamptothecin, and topotecan. We reported previously that estrone and 17beta-estradiol reverse BCRP-mediated multidrug resistance. In the present study, we demonstrate that BCRP exports estrogen metabolites. First, we generated BCRP-transduced LLC-PK1 (LLC/BCRP) cells, in which exogenous BCRP is expressed in the apical membrane, and investigated transcellular transport of 3H-labeled compounds using cells plated on microporous filter membranes. The basal-to-apical transport (excretion) of mitoxantrone, estrone, and 17beta-estradiol was greater in LLC/BCRP cells than in LLC-PK1 cells. Thin-layer chromatography of transported steroids revealed that the transport of estrone and 17beta-estradiol was independent of BCRP expression. Alternatively, increased excretion of estrone sulfate and 17beta-estradiol sulfate was observed in LLC/BCRP cells. BCRP inhibitors completely inhibited the increased excretion of sulfated estrogens across the apical membrane. Conversion of estrogens into their sulfate conjugates was similar between LLC/BCRP and LLC-PK1 cells, suggesting that the increased excretion of estrogen sulfates was attributable to BCRP-mediated transport. Next, the uptake of 3H-labeled compounds in membrane vesicles from BCRP-transduced K562 (K562/BCRP) cells was investigated. 3H-labeled estrone sulfate, but not 3H-labeled estrone or 17beta-estradiol, was taken up by membrane vesicles from K562/BCRP cells, and this was ATP-dependent. Additionally, BCRP inhibitors suppressed the transport of estrone sulfate in membrane vesicles from K562/BCRP cells. These results suggest that BCRP does not transport either free estrone or 17beta-estradiol but exports sulfate conjugates of these estrogens.

DrugBank Data that Cites this Article

Drug Transporters
DrugTransporterKindOrganismPharmacological ActionActions
Conjugated estrogensATP-binding cassette sub-family G member 2ProteinHumans
Unknown
Substrate
Details
EstradiolATP-binding cassette sub-family G member 2ProteinHumans
Unknown
Inhibitor
Details
Estradiol acetateATP-binding cassette sub-family G member 2ProteinHumans
Unknown
Inhibitor
Details
Estradiol benzoateATP-binding cassette sub-family G member 2ProteinHumans
Unknown
Inhibitor
Details
Estradiol cypionateATP-binding cassette sub-family G member 2ProteinHumans
Unknown
Inhibitor
Details
Estradiol dienanthateATP-binding cassette sub-family G member 2ProteinHumans
Unknown
Inhibitor
Details
Estradiol valerateATP-binding cassette sub-family G member 2ProteinHumans
Unknown
Inhibitor
Details
EstroneATP-binding cassette sub-family G member 2ProteinHumans
Unknown
Inhibitor
Details
Hydrocortisone aceponateATP-binding cassette sub-family G member 2ProteinHumans
Unknown
Not AvailableDetails
Hydrocortisone acetateATP-binding cassette sub-family G member 2ProteinHumans
Unknown
Not AvailableDetails
Hydrocortisone butyrateATP-binding cassette sub-family G member 2ProteinHumans
Unknown
Not AvailableDetails
Hydrocortisone cypionateATP-binding cassette sub-family G member 2ProteinHumans
Unknown
Not AvailableDetails
Hydrocortisone phosphateATP-binding cassette sub-family G member 2ProteinHumans
Unknown
Not AvailableDetails
Hydrocortisone probutateATP-binding cassette sub-family G member 2ProteinHumans
Unknown
Not AvailableDetails
Hydrocortisone valerateATP-binding cassette sub-family G member 2ProteinHumans
Unknown
Not AvailableDetails
MitoxantroneATP-binding cassette sub-family G member 2ProteinHumans
Unknown
Substrate
Details
Taurocholic acidATP-binding cassette sub-family G member 2ProteinHumans
Unknown
Inhibitor
Details