Germline mutations of renal cancer predisposition genes and clinical relevance in Chinese patients with sporadic, early-onset disease

被引:25
|
作者
Wu, Junlong [2 ,3 ]
Wang, Hongkai [2 ,3 ]
Ricketts, Christopher J. [1 ]
Yang, Youfeng [1 ]
Merino, Maria J. [1 ]
Zhang, Hailiang [2 ,3 ]
Shi, Guohai [2 ,3 ]
Gan, Hualei [3 ,4 ]
Linehan, W. Marston [1 ]
Zhu, Yao [2 ,3 ]
Ye, Dingwei [2 ,3 ]
机构
[1] NCI, Urol Oncol Branch, Ctr Canc Res, NIH, 10 Ctr Dr,MSC 1107,Room 1-5940, Bethesda, MD 20892 USA
[2] Fudan Univ, Dept Urol, Shanghai Canc Ctr, 270 Dongan Rd, Shanghai 200032, Peoples R China
[3] Fudan Univ, Shanghai Med Coll, Dept Oncol, Shanghai, Peoples R China
[4] Fudan Univ, Dept Pathol, Shanghai Canc Ctr, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
BRCA1-associated protein 1 (BAP1); cancer predisposition; early onset; fumarate hydratase (FH); next-generation sequencing; renal tumor; TUBEROUS SCLEROSIS COMPLEX; PREVALENCE; STATISTICS; MELANOMA; OLAPARIB; TUMORS;
D O I
10.1002/cncr.31908
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background An inherited susceptibility to renal cancers is associated with multiple predisposing genes, but most screening tests are limited to patients with a family history. Next-generation sequencing (NGS)-based multigene panels provide an efficient and adaptable tool for investigating pathogenic germline mutations on a larger scale. This study investigated the frequency of pathogenic germline mutations in renal cancer predisposition genes in patients with sporadic, early-onset disease. Methods An NGS-based panel of 23 known and potential renal cancer predisposition genes was used to analyze germline mutations in 190 unrelated Chinese patients under the age of 45 years who presented with renal tumors. The detected variants were filtered for pathogenicity, and then their frequencies were calculated and correlated with clinical features. Germline variants of the fumarate hydratase (FH) and BRCA1-associated protein 1 (BAP1) genes were comprehensively analyzed because of their aggressive potential. Results In total, 18 patients (9.5%) had germline mutations in 10 genes. Twelve of these 18 patients had alterations in renal cancer predisposition genes (6.3%), and 6 patients had mutations in potential predisposition genes such as BRCA1/2. Notably, pathogenic mutation carriers had a significant family history in second-degree relatives in comparison with those without pathogenic mutations (P < .001). Variants of unknown clinical significance in FH and BAP1 demonstrated evidence of additional somatic loss in tumors. Conclusions In patients with early-onset disease, a multigene panel identified a high pathogenic germline mutation rate in renal cancer predisposition genes. This study emphasizes the importance of screening patients with early-onset disease for mutations in cancer predisposition genes. Germline screening should be encouraged in early-onset patients to provide personalized medicine and improve patient outcomes.
引用
收藏
页码:1060 / 1069
页数:10
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