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美沙酮不会增强阿霉素在犬肿瘤细胞系中的作用。

Methadone does not potentiate the effect of doxorubicin in canine tumour cell lines.

机构信息

Division of Radiation Oncology, Vetsuisse Faculty University of Zurich, Zurich, Switzerland.

Center for Clinical Studies at the Vetsuisse Faculty of the University of Zurich, Zurich,, Switzerland.

出版信息

Vet Med Sci. 2020 Aug;6(3):283-289. doi: 10.1002/vms3.266. Epub 2020 Apr 19.

DOI:10.1002/vms3.266
PMID:32306524
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7397897/
Abstract

Opioid receptor activation was shown to enhance the efficacy of anti-neoplastic drugs in several human cancer cell lines. In these cell lines, doxorubicin increased the number of opioid receptors and methadone concurrently enhanced cellular doxorubicin uptake. Triggered through lay press and media, animal owners started to challenge veterinary oncologists with questions about methadone use in anti-cancer therapy. Especially in veterinary medicine, where side effects of chemotherapy are tolerated to a lesser extent and hence smaller doses are given, agents potentiating chemotherapeutic agents would be an optimal approach to treatment. Canine transitional cell carcinoma cells (TCC, K9TCC), canine osteosarcoma cells (OSA, Abrams) and canine hemangiosarcoma cells (HSA, DAL-4) were incubated with different combinations of methadone, buprenorphine and doxorubicin, in order to test inhibition of cell proliferation. Opioid receptor density was assessed with fluorescence-activated cell sorting in drug native and doxorubicin pretreated cells. In TCC and OSA cell lines opioid receptor density increased after doxorubicin pretreatment. In combination treatment, however, we did not find significant potentiation of doxorubicin's inhibitory effect on proliferation in these cell lines. Neither was there a significant increase of the effect of doxorubicin when the opioids were added 24 hr before doxorubicin. Hence, we could not confirm the hypothesis that opioids increase the anti-proliferative effect of the anti-neoplastic drug doxorubicin in any of these canine tumour cell lines. The lack of effect on a cellular level does not warrant a clinical approach to use opioids together with doxorubicin in dogs with cancer.

摘要

阿片受体激动剂被证明可以增强几种人类癌细胞系中抗肿瘤药物的疗效。在这些细胞系中,阿霉素增加了阿片受体的数量,而美沙酮同时增强了细胞内阿霉素的摄取。在媒体的推动下,动物主人开始向兽医肿瘤学家提出关于美沙酮在癌症治疗中的应用的问题。特别是在兽医领域,化疗的副作用耐受性较低,因此给予的剂量较小,增强化疗药物的药物将是一种理想的治疗方法。犬膀胱移行细胞癌细胞(TCC,K9TCC)、犬骨肉瘤细胞(OSA,Abrams)和犬血管肉瘤细胞(HSA,DAL-4)与不同组合的美沙酮、丁丙诺啡和阿霉素孵育,以测试细胞增殖的抑制作用。用荧光激活细胞分选术在药物天然和阿霉素预处理细胞中评估阿片受体密度。在 TCC 和 OSA 细胞系中,阿霉素预处理后阿片受体密度增加。然而,在联合治疗中,我们没有发现阿霉素对这些细胞系增殖的抑制作用有显著增强。当阿片类药物在阿霉素前 24 小时添加时,也没有观察到阿霉素效果的显著增加。因此,我们无法证实阿片类药物在这些犬肿瘤细胞系中增加抗肿瘤药物阿霉素的抗增殖作用的假设。在细胞水平上没有效果,因此没有理由在患有癌症的狗中使用阿片类药物与阿霉素联合使用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bb3/7397897/5bddf5bf4bbe/VMS3-6-283-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bb3/7397897/d43571eea106/VMS3-6-283-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bb3/7397897/5bddf5bf4bbe/VMS3-6-283-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bb3/7397897/d43571eea106/VMS3-6-283-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bb3/7397897/5bddf5bf4bbe/VMS3-6-283-g002.jpg

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