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Antitumor Activities of IKP‐104 a 4(1H)‐Pyrizinone Derivative on Cultured and Implanted Tumors

机译:IKP-104(4(1H)-吡嗪酮衍生物)对培养和植入的肿瘤的抗肿瘤活性

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摘要

Antitumor activities of IKP‐104, a 4(1H)‐pyrizinone derivative, were investigated with cultured tumor cell lines and implanted tumors in mice. IKP‐104 inhibited the growth of cultured murine tumor cell lines (L1210 leukemia, Lewis lung carcinoma and B16 melanoma) and human tumor cell lines (K562 leukemia and HeLa cervical carcinoma). It also had antitumor effects on implanted murine ascitic tumors (L1210 leukemia and sarcoma 180) and a murine solid tumor (Lewis lung carcinoma). IKP‐104 could be classified as a phase‐dependent cytostatic drug based on the mode of growth inhibition of cultured B16 melanoma cells compared with those of several other antitumor agents. The effect of IKP‐104 on the cell cycle traverse of cultured B16 melanoma cells was estimated by morphological and flow cytometric analyses. Cells accumulated in the mitotic phase, and abortive mitosis or polyploidy or multinucleation was induced from 6 h after exposure to IKP‐104. Based on these results, IKP‐104 is expected to be useful for the treatment of tumors, and its mode of action seemed to be similar to that of metaphase arrestants such as colchicine or vinca alkaloids.
机译:用培养的肿瘤细胞系和植入小鼠的肿瘤研究了IKP-104(一种4(1H)-吡嗪酮衍生物)的抗肿瘤活性。 IKP-104抑制培养的鼠类肿瘤细胞系(L1210白血病,Lewis肺癌和B16黑色素瘤)和人肿瘤细胞系(K562白血病和HeLa宫颈癌)的生长。它还对植入的小鼠腹水肿瘤(L1210白血病和肉瘤180)和小鼠实体瘤(Lewis肺癌)具有抗肿瘤作用。与其他几种抗肿瘤药物相比,根据培养的B16黑色素瘤细胞的生长抑制方式,IKP-104可以归为阶段依赖性细胞生长抑制药物。通过形态学和流式细胞术分析评估了IKP-104对培养的B16黑色素瘤细胞的细胞周期遍历的影响。暴露于IKP-104后6小时,诱导细胞在有丝分裂期积聚,并引起流产的有丝分裂或多倍体或多核化。基于这些结果,预计IKP-104可用于治疗肿瘤,其作用方式似乎与秋水仙碱或长春花生物碱等中期杀伤剂相似。

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