首页> 外文期刊>The Journal of Urology >Antitumor effects of imidazoquinolines in urothelial cell carcinoma of the bladder.
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Antitumor effects of imidazoquinolines in urothelial cell carcinoma of the bladder.

机译:咪唑并喹啉类药物在膀胱尿路上皮细胞癌中的抗肿瘤作用。

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PURPOSE: Imidazoquinolines (Toll-like receptor-7 agonists) are a class of synthetic immune modulating agents. Imiquimod, a member of this drug family, is currently used as first line topical therapy for genital condyloma. It recently showed clinical efficacy against several benign and malignant skin lesions, including actinic keratosis and basal cell carcinoma. Working primarily through the stimulation of a proinflammatory immune response, the mechanism of action of imiquimod may be similar to that through which bacillus Calmette-Guerin is thought to act. We hypothesized that imidazoquinolines have therapeutic potential against bladder cancer. We determined the in vitro and in vivo effects of imidazoquinolines against bladder cancer cells. MATERIALS AND METHODS: The human and murine J82, T24, TCC-SUP (American Tissue Culture Collection, Manassas, Virginia) and MBT-2 bladder cancer cell lines were cultured in normal culture medium or medium supplemented with imidazoquinoline. Effects on cell viability, apoptosis induction and cytokine production were evaluated. In addition, the effects of imidazoquinoline on in vivo bladder tumor growth were determined via intravesical instillation in an orthotopic bladder tumor model in the mouse. RESULTS: A dose dependent decrease in cell viability was observed in all tumor cell lines treated with imidazoquinoline. In addition, imidazoquinoline significantly induced apoptosis and cytokine production. In in vivo experiments most mice treated with imidazoquinoline showed only an intense inflammatory response with no evidence of tumor, while control mice showed tumor growth. CONCLUSIONS: Imidazoquinolines have potent direct activity against bladder cancer cells by decreasing cell viability and inducing apoptosis and cytokine production. In addition, in vivo data suggest antitumor effects in an orthotopic bladder cancer mouse model. Therefore, imidazoquinolines may have therapeutic potential as a synthetic intravesical agent against bladder cancer.
机译:用途:咪唑并喹啉(Toll样受体7激动剂)是一类合成的免疫调节剂。该药物家族的成员咪喹莫特目前被用作生殖器尖锐湿疣的一线局部治疗。最近它显示出对多种良性和恶性皮肤病变的临床疗效,包括光化性角化病和基底细胞癌。咪喹莫特的作用机理主要是通过刺激促炎性免疫反应而起作用,其作用机理可能类似于认为卡介苗-卡林芽孢杆菌起作用的机理。我们假设咪唑并喹啉具有治疗膀胱癌的潜力。我们确定了咪唑喹啉类药物对膀胱癌细胞的体外和体内作用。材料与方法:将人和鼠J82,T24,TCC-SUP(美国组织培养收藏,弗吉尼亚州马纳萨斯)和MBT-2膀胱癌细胞系在正常培养基或添加咪唑并喹啉的培养基中培养。评估了对细胞活力,凋亡诱导和细胞因子产生的影响。此外,通过在小鼠原位膀胱肿瘤模型中膀胱内滴注确定咪唑并喹啉对体内膀胱肿瘤生长的影响。结果:在用咪唑喹啉处理的所有肿瘤细胞系中均观察到细胞活力的剂量依赖性降低。此外,咪唑并喹啉可显着诱导细胞凋亡和细胞因子的产生。在体内实验中,大多数用咪唑并喹啉处理的小鼠仅表现出强烈的炎症反应,没有肿瘤的迹象,而对照小鼠则表现出肿瘤的生长。结论:咪唑喹啉类药物通过降低细胞活力并诱导细胞凋亡和细胞因子产生,具有对膀胱癌细胞有效的直接活性。另外,体内数据表明在原位膀胱癌小鼠模型中具有抗肿瘤作用。因此,咪唑并喹啉作为合成的膀胱内膀胱癌治疗剂可能具有治疗潜力。

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