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首页> 外文期刊>Biochemical Pharmacology >Inhibition of microtubule polymerization by 3-bromopropionylamino benzoylurea (JIMB01), a new cancericidal tubulin ligand.
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Inhibition of microtubule polymerization by 3-bromopropionylamino benzoylurea (JIMB01), a new cancericidal tubulin ligand.

机译:3-溴丙酰氨基苯甲酰脲(JIMB01)(一种新的抗癌微管蛋白配体)抑制微管聚合。

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摘要

3-Bromopropionylamino benzoylurea (JIMB01) is a small molecular weight compound (MW 313) that has been synthesized in our laboratory. This compound showed antiproliferative activities in a panel of thirteen human tumor cell lines with IC(50) values in the range of 0.25 to 0.51 micro M for leukemia and lymphoma cell lines and 0.33 to 9.26 micro M for solid tumor cell lines. The primary action of JIMB01 is to inhibit microtubule polymerization but not depolymerization. A 4 micro M concentration of the compound caused a complete inhibition of microtubule assembly in a cell-free reaction. An increase in the number of human hepatocarcinoma cells blocked in the M-phase was detected 12hr after exposure to JIMB01. The kinase activity of cyclin B1, which is responsible for the G(2)/M transition, was increased accordingly. Bcl-2 phosphorylation became visible, in a western blot, within 6hr in hepatocarcinoma cells treated with JIMB01 at 0.8 micro M or higher. JIMB01-induced apoptosis in liver cancer cells was confirmed by morphological methods, flow cytometry, as well as DNA gel electrophoresis, which clearly demonstrated DNA degradation in the form of a multiple-unit DNA ladder. Furthermore, in vivo experiments using nude mice showed that intraperitoneal injection of JIMB01 at 15mg/kg (with seven injections at 4-day intervals) significantly inhibited the growth of a human hepatocarcinoma (BEL-7402) by 66% in tumor volume (P=0.01), at least compatible to the inhibition by vincristine (43% inhibition), indicating good bioavailability of the compound in the circulation. Side-effects of the compound were not observed, and the body weight of the treated mice remained stable during the 4-week treatment. Since JIMB01 is a small compound, targets a specific molecule in tumor cells, and has promising activity against human hepatocarcinoma in vivo, we believe JIMB01 merits consideration for further investigation.
机译:3-溴丙酰氨基苯甲酰脲(JIMB01)是在我们实验室合成的小分子量化合物(MW 313)。该化合物在13种人类肿瘤细胞系中显示出抗增殖活性,对于白血病和淋巴瘤细胞系,IC(50)值在0.25至0.51 micro M范围内;对于实体肿瘤细胞系,IC(50)值在0.33至9.26 micro M范围内。 JIMB01的主要作用是抑制微管聚合,但不能解聚。该化合物的浓度为4 micro M,导致在无细胞反应中完全抑制了微管装配。暴露于JIMB01后12小时,检测到在M期受阻的人肝癌细胞数量增加。相应地增加了负责G(2)/ M过渡的细胞周期蛋白B1的激酶活性。在Western印迹中,在0.8 micro M或更高的JIMB01处理的肝癌细胞中,Bcl-2磷酸化在6小时之内变得可见。 JIMB01诱导的肝癌细胞凋亡已通过形态学方法,流式细胞术以及DNA凝胶电泳得到了证实,这清楚地证明了DNA降解为多单元DNA阶梯形式。此外,使用裸鼠进行的体内实验表明,腹膜内注射JIMB01的剂量为15mg / kg(每隔4天注射7次),可显着抑制人肝癌(BEL-7402)的生长,其肿瘤体积达到66%(P = 0.01),至少与长春新碱的抑制作用相容(抑制43%),表明该化合物在循环中具有良好的生物利用度。没有观察到该化合物的副作用,并且在4周的治疗过程中,治疗小鼠的体重保持稳定。由于JIMB01是小的化合物,靶向肿瘤细胞中的特定分子,并且在体内具有抗人肝癌的良好活性,因此我们认为JIMB01值得进一步研究。

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