Abstract
Background:
In order to understand the cross-resistance between epirubicin (EPI) and mitoxantrone (MIT), EPI- and MIT-resistant cells were established and their cross-resistance was evaluated.
Materials and methods:
The degrees of growth inhibition of EPI-resistant HLE-EPI cells and MIT-resistant HLE-MIT cells by anticancer drugs were measured. The mRNA expressions of multidrug resistance protein 1 (MDR1)/ABCB1 and breast cancer resistance protein (BCRP)/ABCG2 were also measured by quantitative real-time RT-PCR. Moreover, intracellular accumulation of EPI was investigated.
Results:
HLE-EPI cells were resistant to EPI, MIT and docetaxel. HLE-MIT cells were resistant to EPI, MIT and SN-38. HLE-EPI cells overexpressed MDR1 and HLE-MIT cells overexpressed BCRP. The intracellular accumulation of EPI was decreased in HLE-EPI and HLE-MIT cells.
Conclusion:
The results suggest that both MDR1 and BCRP can up-regulate the efflux of EPI causing resistance to EPI in HLE-EPI and HLE-MIT cells.
MeSH terms
-
ATP Binding Cassette Transporter, Subfamily B, Member 1 / biosynthesis
-
ATP Binding Cassette Transporter, Subfamily B, Member 1 / genetics
-
ATP Binding Cassette Transporter, Subfamily G, Member 2
-
ATP-Binding Cassette Transporters / biosynthesis*
-
ATP-Binding Cassette Transporters / genetics
-
Antibiotics, Antineoplastic / pharmacology
-
Carcinoma, Hepatocellular / drug therapy*
-
Carcinoma, Hepatocellular / genetics
-
Carcinoma, Hepatocellular / metabolism*
-
Drug Resistance, Multiple
-
Drug Resistance, Neoplasm
-
Epirubicin / pharmacokinetics
-
Epirubicin / pharmacology*
-
Humans
-
Liver Neoplasms / drug therapy*
-
Liver Neoplasms / genetics
-
Liver Neoplasms / metabolism*
-
Mitoxantrone / pharmacokinetics
-
Mitoxantrone / pharmacology*
-
Neoplasm Proteins / biosynthesis
-
Neoplasm Proteins / genetics
-
RNA, Messenger / biosynthesis
-
RNA, Messenger / genetics
-
Reverse Transcriptase Polymerase Chain Reaction
-
Tumor Cells, Cultured
Substances
-
ABCG2 protein, human
-
ATP Binding Cassette Transporter, Subfamily B, Member 1
-
ATP Binding Cassette Transporter, Subfamily G, Member 2
-
ATP-Binding Cassette Transporters
-
Antibiotics, Antineoplastic
-
Neoplasm Proteins
-
RNA, Messenger
-
Epirubicin
-
Mitoxantrone