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Aspirin lysine mifepristone and doxycycline combined can effectively and safely prevent and treat cancer metastasis: prevent seeds from gemmating on soil

机译:阿司匹林赖氨酸米非司酮和多西环素合用可有效安全地预防和治疗癌症转移:防止种子在土壤上结块

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摘要

Recent scientific advances have increased our understanding of the cancer metastatic complexities and provided further impetus for new combination therapies to prevent cancer metastasis. Here, we demonstrated that a combination (HAMPT) of aspirin, lysine, mifepristone and doxycycline can effectively and safely prevent cancer metastasis. The pharmaceutically-formulated HAMPT inhibited adhesion of cancer cells to either endothelial cells or extracellular matrix via down-regulating cell adhesion molecules ICAM-1 and α4-integrin. HAMPT inhibited the cloak effect by activated platelets on cancer cells, thereby interfering adhesion and invasion of cancer cells to the underlying stroma. At the effective concentration, HAMPT induced cancer cells into dormancy with minor inhibition on cell viability. Four-day pretreatment followed by 30-day oral administration of HAMPT (33.5-134 mg/kg) to the mice inoculated with cancer cells produced significant inhibition on cancer metastasis dose-dependently without marked side effects. Fifty-day rat toxicity study with HAMPT at doses (335-1340 mg/kg) 20-fold higher than its therapeutic dose produced no significant toxicity. Interestingly, the acute toxic death could not be reached at the maximum administrable dose (5 g/kg). This proof-of-concept study provides the first conceptual evidence that cancer metastasis can be controlled by using affordable old drugs to restrain circulating tumor cells from gemmating on the metastatic soil without the need for cytotoxicity.
机译:最近的科学进展增加了我们对癌症转移复杂性的了解,并为预防癌症转移的新联合疗法提供了进一步的动力。在这里,我们证明了阿司匹林,赖氨酸,米非司酮和多西环素的组合(HAMPT)可以有效,安全地预防癌症转移。药物配制的HAMPT通过下调细胞粘附分子ICAM-1和α4-整联蛋白来抑制癌细胞与内皮细胞或细胞外基质的粘附。 HAMPT通过活化的血小板抑制癌细胞的隐身效果,从而干扰癌细胞对基础基质的粘附和侵袭。在有效浓度下,HAMPT诱导癌细胞进入休眠状态,对细胞活力的抑制作用很小。经过四天的预处理,然后对接种癌细胞的小鼠口服HAMPT(33.5-134 mg / kg)30天,剂量依赖性地显着抑制了癌症转移,没有明显的副作用。用HAMPT剂量(335-1340 mg / kg)高出其治疗剂量20倍的五十天大鼠毒性研究未产生明显的毒性。有趣的是,在最大给药剂量(5 g / kg)下无法达到急性毒性死亡。这项概念验证研究提供了第一个概念性证据,即可以通过使用负担得起的旧药抑制循环肿瘤细胞在转移性土壤上成块生长而无需细胞毒性来控制癌症转移。

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