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膀胱癌患者卡介苗治疗后诱导型一氧化氮合酶的定位和表达。

Localization and expression of inducible nitric oxide synthase in patients after BCG treatment for bladder cancer.

机构信息

Department of Molecular Medicine and Surgery, Section of Urology, Karolinska Institutet, Stockholm, Sweden.

出版信息

Nitric Oxide. 2012 Oct 15;27(3):185-91. doi: 10.1016/j.niox.2012.07.001. Epub 2012 Jul 20.

Abstract

Treatment with Bacillus Calmette Guerin (BCG) bladder instillations is an established treatment modality for superficial urinary bladder cancer and carcinoma in situ (CIS), but the anti-tumor mechanisms following BCG instillations remain largely unknown. Previous data show increased nitric oxide (NO) concentrations in the urinary bladder from patients treated with BCG suggesting that NO-formation may be involved in the BCG mediated effect. In the present study we evaluated 11 patients with urinary bladder cancer who had received BCG treatment and 11 tumor free control subjects. We performed immunohistochemistry, Western blot and real-time polymerase chain reaction (PCR) on bladder biopsies to establish inducible nitric oxide synthase (iNOS) protein levels and localization as well as iNOS mRNA expression. Endogenous NO formation in the bladder was also measured. In patients with bladder cancer who had received BCG treatment iNOS-like immunoreactivity was found in the urothelial cells but also in macrophages in the submucosa. Furthermore, endogenously formed NO was significantly increased (p<0.001) in the BCG treated patients and they had a ten-fold increase in mRNA expression for iNOS compared to healthy controls (p=0.003). In conclusion iNOS was found to be localized to the urothelium and macrophages underlying it. Our study also confirms elevated levels of endogenously formed NO and increased mRNA expression and protein levels for iNOS in patients with BCG treated bladder cancer. These data further support the notion that NO may be involved in the anti-tumor mechanism that BCG exerts on bladder cancer cells.

摘要

卡介苗膀胱内灌注是治疗表浅性膀胱癌和原位癌(CIS)的一种既定治疗方法,但卡介苗灌注后的抗肿瘤机制在很大程度上仍不清楚。先前的数据表明,接受卡介苗治疗的患者膀胱中的一氧化氮(NO)浓度增加,这表明 NO 的形成可能与卡介苗介导的作用有关。在本研究中,我们评估了 11 名接受卡介苗治疗的膀胱癌患者和 11 名无肿瘤对照者。我们对膀胱活检进行免疫组织化学、Western blot 和实时聚合酶链反应(PCR),以确定诱导型一氧化氮合酶(iNOS)蛋白水平和定位以及 iNOS mRNA 表达。还测量了膀胱内内源性 NO 的形成。在接受卡介苗治疗的膀胱癌患者中,我们发现尿路上皮细胞和黏膜下层的巨噬细胞中存在 iNOS 样免疫反应性。此外,在接受卡介苗治疗的患者中,内源性形成的 NO 显著增加(p<0.001),与健康对照组相比,iNOS 的 mRNA 表达增加了十倍(p=0.003)。总之,iNOS 定位于尿路上皮及其下的巨噬细胞。我们的研究还证实,接受卡介苗治疗的膀胱癌患者的内源性形成的 NO 水平升高,iNOS 的 mRNA 表达和蛋白水平增加。这些数据进一步支持了这样一种观点,即 NO 可能参与了卡介苗对膀胱癌细胞发挥的抗肿瘤机制。

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