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Correlation study showing no concordance between EPAS-1/HIF-2alpha mRNA and protein expression in transitional cellcancer of the bladder.

机译:相关性研究显示EPAS-1 / HIF-2alpha mRNA与膀胱移行细胞癌中的蛋白表达之间没有一致性。

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OBJECTIVES: Endothelial Per-ARNT-Sim (PAS) domain protein-1 (EPAS-1)/hypoxia-inducible factor (HIF)-2alpha is a recently identified, endothelial-specific, hypoxia-induced transcription factor and is reputed to have an important role in tumor angiogenesis and tumor progression. Only a few studies have reported on the clinical correlation with grade, stage, necrosis, and microvessel density in transitional cell carcinoma of the bladder. In vitro studies have reported no concordance of EPAS-1/HIF-2alpha mRNA and protein expression. We sought to elucidate these two issues. METHODS: Surgical specimens from 110 patients with transitional cell carcinoma comprised the study, including 51 from radical cystectomy and 59 from transurethral resection of bladder tumor. Immunohistochemistry and in situ hybridization were performed with antibodies against EPAS-1/HIF-2alpha, CD31, and a human EPAS-1/HIF-2alpha cDNA subclone probe. RESULTS: EPAS-1/HIF-2alpha protein expression was found almost exclusively in high-gradeand high-stage tumors (P <0.0001). EPAS-1/HIF-2alpha mRNA expression was detectable only in high-grade (grade 3) and high-stage (pT3a or greater) cases with positive EPAS-1/HIF-2alpha protein expression (P = 0.0017). The presence of necrosis correlated with EPAS-1/HIF-2alpha expression, tumor grade, and tumor stage (P <0.0001). Microvessel density was much lower in invasive, larger tumor nodules in EPAS-1/HIF-2alpha-positive cases than in the negative cases (P <0.0001). CONCLUSIONS: EPAS-1/HIF-2alpha protein and mRNA levels correlate with higher grade and advanced bladder transitional cell carcinoma. In lower stage cases, no concordance was found between transcription and translation of EPAS-1/HIF-2alpha gene expression. Because EPAS-1/HIF-2alpha mRNA is only detectable in highly invasive cancer cases, it may serve as a therapeutic target (eg, by an antisense mRNA approach) for bladder cancer.
机译:目的:内皮-ARNT-Sim(PAS)域蛋白-1(EPAS-1)/低氧诱导因子(HIF)-2alpha是最近鉴定的内皮特异性低氧诱导的转录因子,据称具有在肿瘤血管生成和肿瘤进展中起重要作用。仅有几项研究报道了膀胱移行细胞癌与等级,分期,坏死和微血管密度的临床相关性。体外研究表明,EPAS-1 / HIF-2alpha mRNA和蛋白质表达没有一致性。我们试图阐明这两个问题。方法:本研究来自110例移行细胞癌患者的手术标本,其中51例行根治性膀胱切除术,59例行经尿道膀胱肿瘤切除术。使用针对EPAS-1 / HIF-2alpha,CD31和人EPAS-1 / HIF-2alpha cDNA亚克隆探针的抗体进行免疫组织化学和原位杂交。结果:EPAS-1 / HIF-2alpha蛋白表达仅在高级别和高分期的肿瘤中发现(P <0.0001)。 EPAS-1 / HIF-2alpha mRNA表达仅在EPAS-1 / HIF-2alpha蛋白表达阳性的高级别(3级)和高阶段(pT3a或更高)的情况下可检测到(P = 0.0017)。坏死的存在与EPAS-1 / HIF-2alpha表达,肿瘤等级和肿瘤分期相关(P <0.0001)。 EPAS-1 / HIF-2alpha阳性病例中,浸润性较大肿瘤结节中的微血管密度比阴性病例低得多(P <0.0001)。结论:EPAS-1 / HIF-2alpha蛋白和mRNA水平与高级别和晚期膀胱移行细胞癌相关。在较低阶段的情况下,在EPAS-1 / HIF-2alpha基因表达的转录和翻译之间未发现一致性。因为EPAS-1 / HIF-2alpha mRNA仅在高度浸润性癌症病例中可检测到,所以它可以作为膀胱癌的治疗靶标(例如,通过反义mRNA方法)。

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