Alchoueiry Michel, Cornejo Kristine, Henske Elizabeth P
Pulmonary and Critical Care Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Pathology Department, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Semin Diagn Pathol. 2024 Jan;41(1):1-7. doi: 10.1053/j.semdp.2023.11.002. Epub 2023 Nov 17.
Multiple hereditary syndromes predispose to kidney cancer, including Von Hippel-Lindau syndrome, BAP1-Tumor Predisposition Syndrome, Hereditary Papillary Renal Cell Carcinoma, Tuberous Sclerosis Complex, Birt-Hogg-Dubé 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.
多种遗传性综合征易患肾癌,包括冯·希佩尔-林道综合征、BAP1肿瘤易感综合征、遗传性乳头状肾细胞癌、结节性硬化症复合体、Birt-Hogg-Dubé综合征、遗传性副神经节瘤-嗜铬细胞瘤综合征、延胡索酸水合酶肿瘤易感综合征和考登综合征。在某些情况下,导致遗传性肾癌的基因突变与散发性肾细胞癌(RCC)中相似的组织学特征紧密相关。例如,透明细胞RCC发生于遗传性综合征VHL中,而散发性透明细胞RCC通常存在VHL基因失活。相比之下,Birt-Hogg-Dube综合征的致病基因FLCN的突变在散发性RCC中很少见。在此,我们聚焦于连接遗传性和散发性RCC的基因及通路。