A Model of the Development of Cisplatin Resistance in Human Small Cell Lung Cancer Xenografts

被引:11
作者
Caffrey, Paula B. [1 ]
Frenkel, Gerald D. [2 ]
Mcandrew, Kathryn L. [1 ]
Marks, Kenneth [3 ]
机构
[1] Calif Univ PA, Dept Biol & Environm Sci, California, PA 15419 USA
[2] Rutgers State Univ, Dept Biol Sci, Newark, NJ USA
[3] Univ Pittsburgh, Magee Womens Res Inst, Med Ctr, Pittsburgh, PA USA
来源
IN VIVO | 2016年 / 30卷 / 06期
关键词
Cisplatin; drug resistance; SCLC; OVARIAN TUMOR XENOGRAFTS; IN-VIVO EFFICACY; DRUG-RESISTANCE; RAPID DEVELOPMENT; PREVENTION; CHEMOTHERAPY; IMATINIB; GROWTH; VITRO; PANEL;
D O I
10.21873/invivo.10990
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background/Aim: To study the prevention of chemotherapy resistance, we have previously designed models of drug-resistant ovarian cancer. We here report an in vivo model of cisplatin-resistant small cell lung cancer (SCLC). Materials and Methods: Mice bearing H526 SCLC xenografts received intraperitoneal pretreatment with a sub-effective cisplatin dose (0.75-1.5 mg/kg) or no pretreatment (controls). Seven days later, all mice received a higher cisplatin dose (3.0 mg/kg), and tumor response was recorded. Cell cultures initiated from pretreated and control xenografts were tested for cisplatin resistance and for glutathione-S-transferase (GST) activity. Results: Pretreatment with 1.5 mg/kg cisplatin induced resistance to 3.0 mg/kg cisplatin. Cells from a pretreated tumor were cisplatin resistant and had nearly twice the GST activity as cells from a control tumor. Conclusion: Such cells may prove useful for identifying other resistance mechanisms and thus guide the selection of potential preventative agents to be tested in the in vivo model.
引用
收藏
页码:745 / 749
页数:5
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