Kankaya Duygu, Kiremitci Saba, Tulunay Ozden, Baltaci Sumer
Department of Pathology, Medical School of Ankara University, Ankara, Turkey.
Department of Pathology, Medical School of Ankara University, Ankara, Turkey.
Pathol Res Pract. 2015 Jul;211(7):505-12. doi: 10.1016/j.prp.2015.03.002. Epub 2015 Mar 20.
To examine the prognostic significance of Gelsolin, NF-κB, and p53 in clear cell renal cell carcinoma (CRCC), which has an unpredictable behavior and tendency for recurrence and metastasis.
Immunohistochemistry was performed on 100 consecutive cases of CRCC using antibodies against Gelsolin, NF-κB, and p53. Tumors were grouped by nuclear grade (NG) as low NG (NG1, 2) or high NG (NG3, 4), and by pathological stage as localized (pT1, 2) or locally invasive (pT3, 4). Clinical stage was grouped as early stage (stage I, II) or late stage (stage III, IV). Evaluation was based on cytoplasmic (NF-κB(Cyt)) and nuclear (NF-κB(Nuc)) expression for NF-κB, nuclear expression for p53, membranous and cytoplasmic expression for Gelsolin.
Gelsolin expression correlated with high NG (p = 0.001), metastasis (p = 0.003), late stage (p = 0.008), and cancer death (p = 0.001). NF-κB(Cyt) expression correlated with high NG (p = 0.002), perirenal invasion (p = 0.010), local invasion (p = 0.020), and late stage (p= 0.003). NF-κB(Nuc) expression failed to predict the prognosis of CRCC. p53 expression correlated with high NG (p = 0.045), lymphovascular invasion (p = 0.05), metastasis (p = 0.001), late stage (p = 0.028), and cancer death (p = 0.034). However, only Gelsolin was found to correlate with disease-specific survival, (p = 0.006), and neither NF-κB nor p53 showed such relation.
Expressions of Gelsolin, NF-κB(Cyt), and p53 associated with aggressive behavior of CRCC, while Gelsolin expression specifically indicated poor disease-specific survival. The results of the present study served to determine biomarkers for predicting high-risk patients with CRCC, expected to show aggressive phenotype.
探讨凝溶胶蛋白、核因子κB(NF-κB)和p53在透明细胞肾细胞癌(CRCC)中的预后意义,该肿瘤具有不可预测的行为以及复发和转移倾向。
对100例连续的CRCC病例进行免疫组织化学检测,使用抗凝溶胶蛋白、NF-κB和p53的抗体。肿瘤按核分级(NG)分为低核分级(NG1、2)或高核分级(NG3、4),按病理分期分为局限性(pT1、2)或局部浸润性(pT3、4)。临床分期分为早期(I期、II期)或晚期(III期、IV期)。评估基于NF-κB的细胞质(NF-κB(Cyt))和细胞核(NF-κB(Nuc))表达、p53的细胞核表达、凝溶胶蛋白的膜和细胞质表达。
凝溶胶蛋白表达与高核分级(p = 0.001)、转移(p = 0.