ABCG2-overexpressing S1-M1-80 cell xenografts in nude mice keep original biochemistry and cell biological properties.
- Author:
Fang WANG
1
;
Yong-Ju LIANG
;
Xing-Ping WU
;
Xiao-Dong SU
;
Li-Wu FU
Author Information
- Publication Type:Journal Article
- MeSH: ATP Binding Cassette Transporter, Sub-Family G, Member 2; ATP-Binding Cassette Transporters; antagonists & inhibitors; metabolism; Adenosine; analogs & derivatives; pharmacology; Animals; Antineoplastic Agents; pharmacology; Cell Cycle; Cell Line, Tumor; Cell Proliferation; Cell Survival; drug effects; Cisplatin; pharmacology; Colonic Neoplasms; metabolism; pathology; Diketopiperazines; Doxorubicin; metabolism; Drug Resistance, Multiple; Drug Resistance, Neoplasm; Female; Heterocyclic Compounds, 4 or More Rings; Humans; Inhibitory Concentration 50; KB Cells; Male; Mice; Mice, Inbred BALB C; Mice, Nude; Mitoxantrone; pharmacology; Neoplasm Proteins; antagonists & inhibitors; metabolism; Neoplasm Transplantation; Rhodamine 123; metabolism; Topotecan; pharmacology
- From:Chinese Journal of Cancer 2012;31(3):150-158
- CountryChina
- Language:English
- Abstract: S1-M1-80 cells, derived from human colon carcinoma S1 cells, are mitoxantrone-selected ABCG2-overexpressing cells and are widely used in in vitro studies of multidrug resistance(MDR). In this study, S1-M1-80 cell xenografts were established to investigate whether the MDR phenotype and cell biological properties were maintained in vivo. Our results showed that the proliferation, cell cycle, and ABCG2 expression level in S1-M1-80 cells were similar to those in cells isolated from S1-M1-80 cell xenografts (named xS1-M1-80 cells). Consistently, xS1-M1-80 cells exhibited high levels of resistance to ABCG2 substrates such as mitoxantrone and topotecan, but remained sensitive to the non-ABCG2 substrate cisplatin. Furthermore, the specific ABCG2 inhibitor Ko143 potently sensitized xS1-M1-80 cells to mitoxantrone and topotecan. These results suggest that S1-M1-80 cell xenografts in nude mice retain their original cytological characteristics at 9 weeks. Thus, this model could serve as a good system for further investigation of ABCG2-mediated MDR.
