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分子与基因组分析鉴定嫌色细胞肾细胞癌的治疗靶点

Molecular and Genomic Profiling to Identify Actionable Targets in Chromophobe Renal Cell Cancer.

机构信息

Division of Urological Oncology, Department of Surgical Oncology, Fox Chase Cancer Center, Philadelphia, PA, USA.

Division of Hematology and Oncology, Department of Medicine, University of Arizona, Tuscon, AZ, USA.

出版信息

Eur Urol Focus. 2018 Dec;4(6):969-971. doi: 10.1016/j.euf.2017.01.003. Epub 2017 Jan 23.

Abstract

Metastatic chromophobe renal cell cancer (chRCC) is a rare subtype of RCC with no standard treatment. We performed molecular profiling of 12 chRCC cases to identify alterations predictive of response to therapy. Tests included immunohistochemistry assays, fluorescence in situ hybridization, and next-generation sequencing. Analysis identified c-KIT overexpression in 6/9 (67%) samples analyzed, and loss of protein expression of RRM1 and MGMT in 11/12 (92%) and of PTEN in 7/12 samples (58%). Mutations of TP53, PTEN, APC, and VHL genes were identified. In summary, molecular profiling of chRCC identified alterations in genes and protein expression that might provide a mechanistic rationale for off-label use of approved therapies in advanced chRCC, and could guide the design of molecularly targeted clinical trials. PATIENT SUMMARY: In this study, we evaluated samples of a rare type of kidney cancer (chromophobe type) and identified potential genetic markers that could be used to individualize treatment and possibly improve treatment outcomes.

摘要

转移性嫌色细胞肾细胞癌(chRCC)是一种罕见的 RCC 亚型,目前尚无标准治疗方法。我们对 12 例 chRCC 病例进行了分子谱分析,以确定对治疗反应有预测作用的改变。检测包括免疫组织化学检测、荧光原位杂交和下一代测序。分析鉴定出 9 例 chRCC 样本中有 6 例(67%)存在 c-KIT 过表达,12 例样本中有 11 例(92%)存在 RRM1 和 MGMT 蛋白表达缺失,7 例(58%)存在 PTEN 缺失。还鉴定出了 TP53、PTEN、APC 和 VHL 基因突变。总之,对 chRCC 的分子谱分析鉴定出了基因和蛋白表达的改变,这些改变可能为晚期 chRCC 中使用已批准的治疗方法提供非标签使用的机制依据,并指导针对特定基因的临床试验的设计。

患者总结

在这项研究中,我们评估了一种罕见类型的肾癌(嫌色细胞型)的样本,并鉴定出了潜在的遗传标志物,这些标志物可用于个体化治疗,并可能改善治疗效果。

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