强效细胞毒抗菌肽P-3在胃癌治疗中的潜在应用

Shilei Wang, Jinlei Ye, Ying Chen, Z. Cui, Qiping Zheng, S. Shen, Lichun Sun
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引用次数: 0

摘要

胃癌是全球范围内严重威胁人类健康的难治性疾病。不幸的是,它的死亡率在常见癌症中仍然很高。为了开发一种新型的抗胃癌药物,避免传统化疗的副作用,我们在研究中考虑了一种新的药物靶向策略。我们首先选取了一些经典的细胞毒化合物,如ansamitocin P-3 (AP-3)、秋水仙碱和紫杉醇,研究了它们对胃癌细胞生长和肿瘤生长的抑制作用。结果表明,这些化合物具有较强的抑制活性。特别是,AP-3在异种移植小鼠模型中表现出明显的抑瘤作用,同时也观察到其严重的副作用。结果支持AP-3本身很可能不具有药物性,但可能通过偶联到药物传递载体上用于药物偶联物,以增强其抗肿瘤功效并减少其副作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Potential Applications of the Potent Cytotoxic Ansamitocin P-3 in the Treatment of Gastric Carcinoma
Gastric carcinoma is a refractory disease that seriously threatens human health globally. Unfortunately, its mortality is still high among common cancers. In order to develop a new type of anti-gastric cancer drug and avoid side effects of traditional chemotheray, a new drug-targeting strategy was considered in our studies. We firstly selected certain classic cytotoxic compounds such as ansamitocin P-3 (AP-3), colchicine and paclitaxel and investigated their efficacy in the suppression of gastric cancer cell growth and tumor growth. We found that these compounds displayed their potent suppressive activities. Particularly, AP-3 showed its significant tumor suppression in xenograft mouse model, and was also observed with its severe side effects. The results supported that AP-3 itself most likely was not druggable, but might be applied for drug conjugates via coupling it to a drug delivery vehicle to enhance its anti-tumor efficacy and reduce its side effects.
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