Kidney cancer: Links between hereditary syndromes and sporadic tumorigenesis

被引:6
作者
Alchoueiry, Michel [1 ]
Cornejo, Kristine [2 ]
Henske, Elizabeth P. [1 ]
机构
[1] Harvard Med Sch, Brigham & Womens Hosp, Dept Med, Pulm & Crit Care Med, Boston, MA 02115 USA
[2] Harvard Med Sch, Massachusetts Gen Hosp, Pathol Dept, Boston, MA USA
关键词
Kidney; Cancer; Hereditary syndromes; Sporadic; RENAL-CELL CARCINOMA; BIRT-HOGG-DUBE; VON-HIPPEL-LINDAU; TUMOR-SUPPRESSOR GENE; COMPREHENSIVE MOLECULAR CHARACTERIZATION; SOMATIC MUTATIONS; ESC-RCC; FOLLICULIN; GERMLINE; CLASSIFICATION;
D O I
10.1053/j.semdp.2023.11.002
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Multiple hereditary syndromes predispose to kidney cancer, including Von Hippel-Lindau syndrome, BAP1Tumor Predisposition Syndrome, Hereditary Papillary Renal Cell Carcinoma, Tuberous Sclerosis Complex, Birt-Hogg-Dube ' syndrome, Hereditary Paraganglioma-Pheochromocytoma Syndrome, Fumarate Hydratase Tumor Predisposition Syndrome, and Cowden syndrome. In some cases, mutations in the genes that cause hereditary kidney cancer are tightly linked to similar histologic features in sporadic RCC. For example, clear cell RCC occurs in the hereditary syndrome VHL, and sporadic ccRCC usually has inactivation of the VHL gene. In contrast, mutations in FLCN, the causative gene for Birt-Hogg-Dube syndrome, are rarely found in sporadic RCC. Here, we focus on the genes and pathways that link hereditary and sporadic RCC.
引用
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页码:1 / 7
页数:7
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