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恩诺沙星增强了携带突变型和野生型p53的犬骨肉瘤细胞的化疗效果。

Enrofloxacin enhances the effects of chemotherapy in canine osteosarcoma cells with mutant and wild-type p53.

作者信息

York D, Withers S S, Watson K D, Seo K W, Rebhun R B

机构信息

The Comparative Oncology Laboratory and Center for Companion Animal Health, Department of Surgical and Radiological Sciences, School of Veterinary Medicine, University of California-Davis, Davis, CA, USA.

UC Davis School of Veterinary Medicine, William R. Pritchard Veterinary Medical Teaching Hospital, University of California-Davis, Davis, CA, USA.

出版信息

Vet Comp Oncol. 2017 Sep;15(3):1087-1100. doi: 10.1111/vco.12250. Epub 2016 Jun 23.

Abstract

Adjuvant chemotherapy improves survival time in dogs receiving adequate local control for appendicular osteosarcoma, but most dogs ultimately succumb to metastatic disease. The fluoroquinolone antibiotic enrofloxacin has been shown to inhibit survival and proliferation of canine osteosarcoma cells in vitro. Others have reported that fluoroquinolones may modulate cellular responses to DNA damaging agents and that these effects may be differentially mediated by p53 activity. We therefore determined p53 status and activity in three canine osteosarcoma cell lines and examined the effects of enrofloxacin when used alone or in combination with doxorubicin or carboplatin chemotherapy. Moresco and Abrams canine osteosarcoma cell lines contained mutations in p53, while no mutations were identified in the D17 cells or in a normal canine osteoblast cell line. The addition of enrofloxacin to either doxorubicin or carboplatin resulted in further reductions in osteosarcoma cell viability; this effect was apparent regardless of p53 mutational status or downstream activity.

摘要

辅助化疗可延长接受了适当局部控制的犬类肢端骨肉瘤患者的生存时间,但大多数犬最终会死于转移性疾病。氟喹诺酮类抗生素恩诺沙星已被证明在体外可抑制犬骨肉瘤细胞的存活和增殖。其他人报告称,氟喹诺酮类药物可能会调节细胞对DNA损伤剂的反应,并且这些作用可能由p53活性差异介导。因此,我们确定了三种犬骨肉瘤细胞系中的p53状态和活性,并研究了恩诺沙星单独使用或与阿霉素或卡铂化疗联合使用时的效果。Moresco和Abrams犬骨肉瘤细胞系中p53存在突变,而在D17细胞或正常犬成骨细胞系中未发现突变。将恩诺沙星添加到阿霉素或卡铂中会导致骨肉瘤细胞活力进一步降低;无论p53突变状态或下游活性如何,这种效果都很明显。

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