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Evans blue-mediated white-light detection of non-muscle-invasive bladder cancer: A preclinical feasibility and safety study using a rat bladder urothelial cell carcinoma model

机译:埃文斯蓝介导的白光检测非肌肉浸润性膀胱癌:使用大鼠膀胱尿路上皮细胞癌模型的临床前可行性和安全性研究

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摘要

Photodynamic diagnosis (PDD) improves the detection of non-muscle-invasive bladder cancer (NMIBC). However, white-light (WL) cystoscopy remains the technique routinely used in urological clinics. A more cost-effective but equally performant alternative to PDD may encompass the use of an intense tumoritropic dye in combination with WL cystoscopy. Using a preclinical setting, we investigated the practical aspects of the use of Evans blue (EB) dye for the possible future detection of NMIBC using WL cystoscopy. A solution of 1 and 5 mM EB was instilled into healthy and AY-27 tumor-bearing rat bladders. The bladders were then rapidly dissected and the inner walls were inspected for EB using WL stereomicroscopy. EB present in the bladders and the plasma was also quantified using high performance liquid chromatography. To assess the effects of repeated instillations on normal rat bladders, EB was instilled for 7 consecutive days, after which time the bladder wall was investigated histologically. To gain insight into the mechanisms underlying the selective accumulation of EB in malignant urothelium, RNA sequencing of urothelial tissue and subsequent comparative analysis were performed, with a specific focus on cell adhesion. The concentrations of EB were substantially higher in malignant bladders compared with those in healthy bladders, matching the blue staining of the inner bladder wall observed by stereomicroscopy. EB was equally present in the plasma of healthy and tumor-bearing subjects, although at low concentrations. Importantly, EB did not cause any abnormalities in the urothelium after 7 days of repeated instillation in normal rats. RNA sequencing of the urothelium indicated an abnormal expression of several genes related to cell adhesion in malignant urothelium compared with the normal urothelium. Our findings may be important for future clinical developments in the field of diagnostics for bladder cancer. Implementing the more cost-effective protocol of EB instillations in combination with WL cystoscopy may offer a benefit to patients as well as the healthcare system.
机译:光动力学诊断(PDD)改善了非肌肉浸润性膀胱癌(NMIBC)的检测。但是,白光(膀胱)膀胱镜检查仍然是泌尿科诊所常规使用的技术。替代PDD的更具成本效益但性能相同的替代方法可能包括将强促生性染料与WL膀胱镜检查结合使用。使用临床前设置,我们调查了使用埃文斯蓝(EB)染料的实际情况,以便将来使用WL膀胱镜检查检测NMIBC。将1 mM和5 mM EB溶液滴入健康且患有AY-27肿瘤的大鼠膀胱中。然后迅速解剖膀胱,并使用WL立体显微镜检查内壁的EB。膀胱和血浆中的EB也可以通过高效液相色谱法进行定量。为了评估反复滴注对正常大鼠膀胱的影响,连续7天滴注EB,然后组织学检查膀胱壁。为了深入了解EB在恶性尿路上皮中选择性积聚的机制,对尿路上皮组织进行RNA测序和随后的比较分析,特别关注细胞粘附。与健康膀胱相比,恶性膀胱中的EB浓度要高得多,这与立体显微镜观察到的膀胱内壁蓝色染色相匹配。 EB在健康和荷瘤受试者的血浆中均存在,尽管浓度很低。重要的是,在正常大鼠中反复滴注7天后,EB不会引起尿路上皮的任何异常。尿路上皮的RNA测序表明,与正常尿道上皮相比,恶性尿道上皮中与细胞粘附有关的几个基因表达异常。我们的发现对于膀胱癌诊断领域的未来临床发展可能很重要。与EB膀胱镜检查相结合实施更具成本效益的EB滴注方案可能为患者以及医疗系统带来好处。

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