Department of Molecular Pathology, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
International Research Centre for Medical Sciences, Kumamoto University, Kumamoto, Japan.
Histopathology. 2019 Aug;75(2):254-265. doi: 10.1111/his.13866. Epub 2019 Jun 25.
Xp11 rearrangement in renal cell carcinoma (RCC) typically involves gene fusion to the gene encoding transcription factor E3 (TFE3), a member of the microphthalmia-associated transcription factor family on chromosome Xp11.2. Dual-colour break-apart fluorescence in-situ hybridisation (FISH) is recommended to confirm histological diagnoses. Recently, RNA-binding motif protein 10 (RBM10), encoded by a gene on chromosome Xp11.3, was identified as a chimeric partner of TFE3; thus, RBM10-TFE3 fusion results from paracentric inversion. RBM10-TFE3 RCC may yield a false-negative result in FISH analysis of TFE3 expression. The aim of the present study was to investigate the clinicopathological features of RBM10-TFE3 RCC.
Ten patients with RBM10-TFE3 RCC aged 31-71 years were investigated. Histological analysis, immunostaining, dual-colour break-apart FISH for TFE3, reverse transcription polymerase chain reaction and sequencing analysis were performed. No patient had a history of exposure to chemotherapy. Two of these patients died of RCC, and three were alive but developed metastases. Microscopically, the tumours were composed of a mixed architecture of tubulocystic and papillary patterns with scattered psammoma bodies. The tumours showed strong nuclear immunoreactivity for TFE3. FISH showed consistent closely spaced split signals in the RCCs of four patients, and polysomic signals with occasional closely spaced split signals in the RCCs of six patients. Of the latter six patients, five had renal failure, and four developed tumours in kidneys subjected to haemodialysis.
The present study suggests that the carcinogenesis of RBM10-TFE3 RCC in some, but not all, patients may be associated with chronic kidney disease. The aggressive nature of RBM10-TFE3 RCC should be considered, as five patients experienced metastases.
Xp11 重排通常涉及基因融合到基因编码转录因子 E3(TFE3),Xp11.2 染色体上小眼相关转录因子家族的成员。建议使用双色分离荧光原位杂交(FISH)来确认组织学诊断。最近,RNA 结合基序蛋白 10(RBM10),由 Xp11.3 染色体上的基因编码,被鉴定为 TFE3 的嵌合伴侣;因此,RBM10-TFE3 融合是由旁中心倒位引起的。RBM10-TFE3 RCC 可能导致 TFE3 表达的 FISH 分析呈假阴性结果。本研究旨在探讨 RBM10-TFE3 RCC 的临床病理特征。
研究了 10 例年龄 31-71 岁的 RBM10-TFE3 RCC 患者。进行了组织学分析、免疫染色、TFE3 的双色分离 FISH、逆转录聚合酶链反应和测序分析。没有患者有化疗暴露史。其中 2 例患者死于 RCC,3 例患者存活但发生转移。显微镜下,肿瘤由管状囊性和乳头状模式的混合结构组成,散布着沙粒体。肿瘤的 TFE3 核免疫反应强烈。FISH 显示 4 例 RCC 的信号紧密分离,6 例 RCC 的信号多倍体,偶尔出现紧密分离的信号。在后者 6 例患者中,有 5 例患者出现肾衰竭,有 4 例患者在接受血液透析的肾脏中发生肿瘤。
本研究表明,在一些但不是所有 RBM10-TFE3 RCC 患者中,癌症的发生可能与慢性肾脏病有关。应该考虑 RBM10-TFE3 RCC 的侵袭性,因为有 5 例患者发生了转移。