Department of Pathology, The University of Alabama at Birmingham, WP Building, Suite P230 l 619 19th Street, South, Birmingham, AL, 35249-7331, USA.
Department of Pathology, The Johns Hopkins Medical Institutions, Baltimore, MD, USA.
Virchows Arch. 2019 Jan;474(1):21-27. doi: 10.1007/s00428-018-2468-0. Epub 2018 Oct 18.
Insulin-like growth factor-1 receptor (IGF1R) is a transmembrane tyrosine kinase receptor that plays a crucial role in cell proliferation, growth, differentiation, and apoptosis. IGF1R overexpression has been observed in several cancers, including invasive bladder carcinomas, as a potential prognostic factor. Given known biologic differences between upper and lower urinary tract urothelial carcinoma, we assessed the expression status and prognostic significance of IGF1R in upper tract urothelial carcinoma (UTUC). Two tissue microarrays (TMAs) were built from 99 Japanese patients with non-metastatic UTUC submitted to radical nephroureterectomy between 1997 and 2011. TMAs were constructed with triplicate tumor and paired benign urothelium. Membranous IGF1R staining was evaluated using immunohistochemistry. Two scoring methods were applied (Her2-score and H-score). The highest score was assigned to each tumor. IGF1R positivity was defined as Her2-score ≥ 1+. Association with clinicopathologic parameters and outcome was assessed using hazard ratios (HR) with 95% confidence intervals (CI) and adjusted P values. We found positive IGF1R expression in 70% of UTUC. Outcomes were as follows: tumor recurrence, 33%; tumor progression, 59%; overall mortality, 33%; and cancer-specific mortality, 30%. IGF1R was not associated with any clinicopathologic features. In addition, IGF1R expression was not associated with tumor recurrence (HR = 0.54, CI = 0.25-1.1, P = 0.11), tumor progression (HR = 1.6, CI = 0.8-3.1, P = 0.19), overall mortality (HR = 1.5, CI = 0.68-3.4, P = 0.31), or cancer-specific mortality (HR = 1.6, CI = 0.68-3.8, P = 0.27). Positive IGF1R expression was found in more than two thirds of UTUC. This finding provides a rationale to investigate IGF1R as a potential therapeutic target in UTUC. In contrast to bladder cancer, IGF1R expression in UTUC did not correlate with outcome, further pointing to biologic differences between UTUC and bladder cancer.
胰岛素样生长因子-1 受体 (IGF1R) 是一种跨膜酪氨酸激酶受体,在细胞增殖、生长、分化和凋亡中发挥着关键作用。在包括浸润性膀胱癌在内的几种癌症中,已经观察到 IGF1R 过表达,它是一种潜在的预后因素。鉴于上尿路尿路上皮癌和下尿路尿路上皮癌之间已知的生物学差异,我们评估了 IGF1R 在尿路上皮癌(UTUC)中的表达状态和预后意义。我们从 1997 年至 2011 年间接受根治性肾输尿管切除术的 99 例日本非转移性 UTUC 患者中建立了两个组织微阵列 (TMA)。TMA 由 3 个复制品肿瘤和配对的良性尿路上皮组成。使用免疫组织化学评估膜 IGF1R 染色。应用了两种评分方法(Her2 评分和 H 评分)。每个肿瘤都被分配了最高的分数。IGF1R 阳性定义为 Her2 评分≥1+。使用危险比 (HR) 及其 95%置信区间 (CI) 和调整后的 P 值评估与临床病理参数和结果的关联。我们发现 70%的 UTUC 存在阳性 IGF1R 表达。结果如下:肿瘤复发,33%;肿瘤进展,59%;总死亡率,33%;癌症特异性死亡率,30%。IGF1R 与任何临床病理特征均无关。此外,IGF1R 表达与肿瘤复发(HR=0.54,CI=0.25-1.1,P=0.11)、肿瘤进展(HR=1.6,CI=0.8-3.1,P=0.19)、总死亡率(HR=1.5,CI=0.68-3.4,P=0.31)或癌症特异性死亡率(HR=1.6,CI=0.68-3.8,P=0.27)均无关。超过三分之二的 UTUC 存在阳性 IGF1R 表达。这一发现为将 IGF1R 作为 UTUC 的潜在治疗靶点提供了依据。与膀胱癌不同,UTUC 中的 IGF1R 表达与结局无关,进一步指出 UTUC 和膀胱癌之间存在生物学差异。