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一种新型的4,4'-联吡啶-5,5'-全氟烷基-2,2'-双恶唑,具有通过细胞周期阻滞和诱导凋亡产生的抗肿瘤活性。

A novel 4,4'-bispyridyl-5,5'-perfluoroalkyl-2,2'-bisoxazol with antitumoral activity via cell cycle arrest and induction of apoptosis.

作者信息

Báñez-Coronel Mónica, Rodríguez-González Agustín, Martín-Cantalejo Yolanda, Sáez Beatriz, Soto Javier, Villa M Jesús, Braña Miguel F, Lacal Juan Carlos

机构信息

Instituto de Investigaciones Biomédicas, CSIC, 28029 Madrid, Spain.

出版信息

Int J Oncol. 2004 Oct;25(4):1097-103.

Abstract

The compound 6a is a novel bisoxazol derivative with high cytotoxic properties in vitro against different human tumor-derived cell lines and with similar efficiency against epithelial, haematopoietic and mesenchymal tumor cells. Although the molecular mechanism is not yet fully defined, cell cycle analysis revealed that 6a induces efficiently G0/G1 phase arrest in colon adenocarcinoma HT-29 cells in a dose- and time-dependent manner. Induction of cell death is observed, a possible explanation for the antiproliferative profile of the molecule. The compound was well tolerated at doses that allowed to examine its antitumor activity against human xenografts of the HT-29 cell line implanted s.c. in nude mice. Treatment of mice with 4 mg/kg of the compound resulted in a 60% inhibition of tumor growth. These observations support the use of 6a for the generation of more potent derivatives that could be used as new anticancer agents.

摘要

化合物6a是一种新型双恶唑衍生物,在体外对不同的人肿瘤衍生细胞系具有高细胞毒性,对上皮、造血和间充质肿瘤细胞的作用效率相似。虽然分子机制尚未完全明确,但细胞周期分析显示,6a以剂量和时间依赖性方式有效地诱导结肠腺癌HT-29细胞的G0/G1期阻滞。观察到细胞死亡的诱导,这可能是该分子抗增殖特性的一种解释。该化合物在允许检测其对皮下植入裸鼠的HT-29细胞系人异种移植瘤抗肿瘤活性的剂量下耐受性良好。用4mg/kg该化合物处理小鼠导致肿瘤生长抑制60%。这些观察结果支持使用6a来生成更有效的衍生物,这些衍生物可作为新型抗癌药物。

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