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对《肾乳头状细胞癌的综合分子特征分析》的述评。癌症基因组图谱研究网络。《新英格兰医学杂志》。2016年1月14日;374(2):135 - 145。

Commentary on: "Comprehensive molecular characterization of papillary renal-cell carcinoma." Cancer Genome Atlas Research Network.: N Engl J Med. 2016 Jan 14;374(2):135-45.

作者信息

Lee Byron H

出版信息

Urol Oncol. 2017 Sep;35(9):578-579. doi: 10.1016/j.urolonc.2017.07.022. Epub 2017 Aug 2.

Abstract

BACKGROUND

Papillary renal-cell carcinoma, which accounts for 15%-20% of renal-cell carcinomas, is a heterogeneous disease that consists of various types of renal cancer, including tumors with indolent, multifocal presentation, and solitary tumors with an aggressive, highly lethal phenotype. Little is known about the genetic basis of sporadic papillary renal-cell carcinoma, and no effective forms of therapy for advanced disease exist.

METHODS

We performed comprehensive molecular characterization of 161 primary papillary renal-cell carcinomas, using whole-exome sequencing, copy-number analysis, messenger RNA and microRNA sequencing, DNA-methylation analysis, and proteomic analysis.

RESULTS

Types 1 and 2 papillary renal-cell carcinomas were shown to be different types of renal cancer characterized by specific genetic alterations, with type 2 further classified into 3 individual subgroups on the basis of molecular differences associated with patient survival. Type 1 tumors were associated with MET alterations, whereas type 2 tumors were characterized by CDKN2A silencing, SETD2 mutations, TFE3 fusions, and increased expression of the NRF2-antioxidant response element (ARE) pathway. A CpG island methylator phenotype was observed in a distinct subgroup of type 2 papillary renal-cell carcinomas that was characterized by poor survival and mutation of the gene encoding fumarate hydratase.

CONCLUSIONS

Types 1 and 2 papillary renal-cell carcinomas were shown to be clinically and biologically distinct. Alterations in the MET pathway were associated with type 1, and activation of the NRF2-ARE pathway was associated with type 2; CDKN2A loss and CpG island methylator phenotype in type 2 conveyed a poor prognosis. Furthermore, type 2 papillary renal-cell carcinoma consisted of at least 3 subtypes based on molecular and phenotypic features. (Funded by the National Institutes of Health.).

摘要

背景

乳头状肾细胞癌占肾细胞癌的15%-20%,是一种异质性疾病,由多种类型的肾癌组成,包括表现为惰性、多灶性的肿瘤以及具有侵袭性、高致死性表型的孤立肿瘤。关于散发性乳头状肾细胞癌的遗传基础知之甚少,且不存在针对晚期疾病的有效治疗方法。

方法

我们使用全外显子测序、拷贝数分析、信使核糖核酸和微小核糖核酸测序、DNA甲基化分析以及蛋白质组分析,对161例原发性乳头状肾细胞癌进行了全面的分子特征分析。

结果

1型和2型乳头状肾细胞癌被证明是具有特定基因改变特征的不同类型肾癌,2型根据与患者生存相关的分子差异进一步分为3个独立亚组。1型肿瘤与MET改变相关,而2型肿瘤的特征是CDKN2A沉默、SETD2突变、TFE3融合以及NRF2-抗氧化反应元件(ARE)途径的表达增加。在2型乳头状肾细胞癌的一个独特亚组中观察到CpG岛甲基化表型,其特征是生存不良和编码延胡索酸水合酶的基因突变。

结论

1型和2型乳头状肾细胞癌在临床和生物学上是不同的。MET途径的改变与1型相关,NRF2-ARE途径的激活与2型相关;2型中的CDKN2A缺失和CpG岛甲基化表型预示着预后不良。此外,2型乳头状肾细胞癌根据分子和表型特征至少由3个亚型组成。(由美国国立卫生研究院资助。)

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