Laboratory Animal and Comparative Medicine ›› 2015, Vol. 35 ›› Issue (5): 367-373.DOI: 10.3969/j.issn.1674-5817.2015.05.005

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Establishment of S180 Tumor Multidrug Resistance Mouse Model by Increasing PFC and Observation on Stability

GU Yun-hao, CAO Chen-jie, HU Bi-yuan, WANG Jun, HAN Dong-dong, XU Ai-hua   

  1. Medical College, Yangzhou University, Yangzhou 225001, China
  • Received:2015-03-03 Online:2015-10-25 Published:2015-10-25

Abstract: Objective To establish aquired S180 multidrug resistance (MDR) mouse model and study on its stability. Methods To mimic the clinical PFC (cis-Dichlorodiamineplatinum+5-Fluorouracil+cyclophosphamide) scheme, gradually increase the dose in three phases to induce S180 ascites tumor mice and establish the aquired S180 MDR mouse model. The induced cells resistance factor to the chemotherapeutics drugs in different stages, the accumulation of adriamycin (ADR) and the functional activity of P-glycoprotein (P-gp) were detected by MTT assay and flow cytometry. And then through detecting the above indicators to monitor the resistance drug stability of induced cells in different stages. The mRNA expression of MDR-1 and multidrug resistance-associated protein 1 (MRP-1) of induced cells in different stages were detected by real time quantitative PCR (RT-qPCR). Results Compared with the parent cells, with induction time extending and dose increasing, the resistance factors in each stage of induced S180 cells to chemotherapeutics drugs were gradually increased, the accumulation of ADR was gradually reduced, and the functional activity of P-gp was strengthened. The mRNA expression of MDR-1 and MRP-1 of induced cells in different stages had a positive correlation to the induction time and dose. The stable resistance time of induced cells in the first, second and third phase are respectively for about 1 week, 2 weeks and 3 weeks. Conclusion To mimic the clinical PFC scheme, using the dose gradually increasing by phased can establish a high resistant strength, long stable time aquired S180MDR experimental model.

Key words: cis-Dichlorodiamineplatinum+5-Fluorouracil+cyclophosphamide (PFC), Multidrug resistance, S180 cell line, in vivo, P-gp, multidrug resistance-1(MDR-1mRNA), multidrug resistance-associated protein-1(MRP-1 mRNA)

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