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NFATc1表达作为上尿路尿路上皮癌预后指标的研究

NFATc1 Expression as a Prognosticator in Urothelial Carcinoma of the Upper Urinary Tract.

作者信息

Kawahara Takashi, Inoue Satoshi, Fujita Kazutoshi, Mizushima Taichi, Ide Hiroki, Yamaguchi Seiji, Fushimi Hiroaki, Nonomura Norio, Miyamoto Hiroshi

机构信息

Departments of Pathology and Urology, Johns Hopkins University School of Medicine, Baltimore, MD, USA; Department of Pathology & Laboratory Medicine, University of Rochester Medical Center, Rochester, NY, USA; Departments of Urology and Renal Transplantation, Yokohama City University Medical Center, Yokohama, Japan.

Departments of Pathology and Urology, Johns Hopkins University School of Medicine, Baltimore, MD, USA; Department of Pathology & Laboratory Medicine, University of Rochester Medical Center, Rochester, NY, USA; James P. Wilmot Cancer Center, University of Rochester Medical Center, Rochester, NY, USA.

出版信息

Transl Oncol. 2017 Jun;10(3):318-323. doi: 10.1016/j.tranon.2017.01.012. Epub 2017 Mar 19.

Abstract

We recently found that NFATc1, a member of the NFAT family and a key regulator of the immune response, could induce bladder carcinogenesis and cancer progression. In this study, we immunohistochemically stained for NFATc1 in upper urinary tract urothelial carcinoma (UUTUC) specimens and paired nonneoplastic urothelial tissues. NFATc1 was positive in 51 [52%; 40 (40%) weak (1+), 9 (9%) moderate (2+), and 2 (2%) strong (3+)] of 99 UUTUCs, which was significantly higher than in benign urothelium [30 (36%) of 83; 28 (34%) weak and 2 (2%) moderate] (0 vs 1+/2+/3+, P=.038; 0/1+ vs 2+/3+, P=.023). There were no significant associations between NFATc1 expression pattern and tumor grade or pT stage. However, the positive rates of NFATc1 expression tended to be higher in renal pelvic tumors (60%) than in ureteral tumors (42%; P=.080) as well as in pN+ tumors (75%) than in pN0 tumors (49%; P=.089). Kaplan-Meier and log-rank tests revealed that moderate (2+) to strong (3+) NFATc1 expression correlated with lower progression-free survival (P=.032) and cancer-specific survival (P=.005) rates in the 99 cases. Patients with high (2+/3+) NFATc1 muscle-invasive tumor (n=9) also had a significantly higher risk of cancer-specific mortality (P=.021) compared to those with low (0/1+) NFATc1 muscle-invasive tumor (n=53). Thus, compared with nonneoplastic urothelium, a significant increase in the expression of NFATc1 in UUTUC was seen, implying the involvement of NFATc1 signals in the development of UUTUC. The current results further suggest that NFATc1 overexpression serves as a predictor of poor prognosis in patients with UUTUC.

摘要

我们最近发现,NFAT家族成员之一且是免疫反应关键调节因子的NFATc1,可诱导膀胱癌发生及癌症进展。在本研究中,我们对肾盂输尿管上皮癌(UUTUC)标本及配对的非肿瘤性尿路上皮组织进行了NFATc1免疫组化染色。99例UUTUC中,51例(52%;40例(40%)弱阳性(1+),9例(9%)中度阳性(2+),2例(2%)强阳性(3+))NFATc1呈阳性,显著高于良性尿路上皮(83例中的30例(36%);28例(34%)弱阳性,2例(2%)中度阳性)(0级与1+/2+/3+级相比,P = 0.038;0/1+级与2+/3+级相比,P = 0.023)。NFATc1表达模式与肿瘤分级或pT分期之间无显著关联。然而,NFATc1表达的阳性率在肾盂肿瘤(60%)中往往高于输尿管肿瘤(42%;P = 0.080),在pN+肿瘤(75%)中高于pN0肿瘤(49%;P = 0.089)。Kaplan-Meier法和对数秩检验显示,在这99例病例中,中度(2+)至强(3+)的NFATc1表达与无进展生存期降低(P = 0.032)及癌症特异性生存率降低(P = 0.005)相关。与低(0/1+)NFATc1肌层浸润性肿瘤(n = 53)患者相比,高(2+/3+)NFATc1肌层浸润性肿瘤(n = 9)患者的癌症特异性死亡风险也显著更高(P = 0.021)。因此,与非肿瘤性尿路上皮相比,UUTUC中NFATc1的表达显著增加,这意味着NFATc1信号参与了UUTUC的发生发展。目前的结果进一步表明,NFATc1过表达可作为UUTUC患者预后不良的预测指标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37aa/5358926/70225e22d46e/gr1.jpg

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