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首页> 外文期刊>Cancer chemotherapy and pharmacology. >Inhibition of established subcutaneous murine tumour growth with topical Melaleuca alternifolia (tea tree) oil.
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Inhibition of established subcutaneous murine tumour growth with topical Melaleuca alternifolia (tea tree) oil.

机译:用局部千层白千层油(茶树油)抑制已建立的皮下鼠肿瘤生长。

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PURPOSE: Systemic toxicity coupled with long treatment regimes of approved topical chemotherapeutic agents such as imiquimod and 5-fluorouracil (5-FU) are limiting. There is now more focus on the potential use of topical terpene agents as skin cancer treatments. Here, we show for the first time that topical Melaleuca alternifolia (tea tree) oil (TTO), abundant in terpenes, has in vivo antitumour activity. METHOD: Topical TTO formulations applied to immunocompetent tumour-bearing mice were assessed for antitumour efficacy by monitoring tumour growth and by histological analysis following treatment. RESULTS: Four, daily, topical treatments of 10% TTO/DMSO regressed subcutaneous AE17 mesotheliomas in mice for a period of 10 days and significantly retarded the growth of subcutaneous B16-F10 melanomas. The antitumour effect of topical 10% TTO/DMSO was accompanied by skin irritation similar to other topical chemotherapeutic agents, but unlike other approved topical agents, quickly and completely resolved. Furthermore, we show that topical 10% TTO/DMSO caused an influx of neutrophils and other immune effector cells in the treated area, with no evidence of systemic toxicity. CONCLUSION: TTO combined with an effective carrier significantly inhibited the growth of aggressive, subcutaneous, chemo-resistant tumours in immunocompetent mice. Taken together, these findings highlight the potential of topical TTO as an alternative topical antitumour treatment.
机译:目的:全身毒性加上长期批准的局部化疗药物(如咪喹莫特和5-氟尿嘧啶(5-FU))的治疗是有限的。现在,人们更加关注局部使用萜烯类药物作为皮肤癌的治疗方法。在这里,我们首次显示出富含萜烯的局部千层草茶油(TTO)具有体内抗肿瘤活性。方法:通过监测肿瘤的生长和治疗后的组织学分析,评估应用于免疫耐受的荷瘤小鼠的局部TTO制剂的抗肿瘤功效。结果:每天四次局部用10%TTO / DMSO进行的治疗使小鼠皮下AE17间皮瘤消退了10天,并显着抑制了皮下B16-F10黑色素瘤的生长。与其他局部化疗药物相似,局部10%TTO / DMSO的抗肿瘤作用伴有皮肤刺激,但与其他已批准的局部药物不同,该反应可快速且完全解决。此外,我们显示局部用10%TTO / DMSO引起治疗区域中性粒细胞和其他免疫效应细胞的大量涌入,而没有全身毒性的证据。结论:TTO与有效载体结合可显着抑制免疫活性小鼠的侵袭性皮下化学耐药性肿瘤的生长。综上所述,这些发现突出了局部TTO作为替代性局部抗肿瘤治疗的潜力。

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