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体细胞VHL改变及其对透明细胞肾细胞癌患者预后的影响。

Somatic VHL alteration and its impact on prognosis in patients with clear cell renal cell carcinoma.

作者信息

Kim Jung Han, Jung Chul Won, Cho Yeon Hee, Lee Jeeyun, Lee Se-Hoon, Kim Ho Young, Park Jinny, Park Joon-Oh, Kim Kihyun, Kim Won Seog, Park Young Suk, Im Young-Hyuck, Kang Won Ki, Park Keunchil

机构信息

Division of Hematology/Oncology, Department of Medicine, Samsung Medical Center, Ilwon-Dong 50, Gangnam-Gu, Seoul 135-710, Korea.

出版信息

Oncol Rep. 2005 May;13(5):859-64.

Abstract

Somatic inactivation of the von Hippel-Lindau (VHL) gene is the most frequent genetic event observed in clear cell renal cell carcinoma (CC-RCC). However, the prognostic relevance of somatic VHL alteration and its target, hypoxia inducible factor (HIF)-1alpha has not been defined. We investigated the genetic changes in the VHL gene and HIF-1alpha and studied their clinical implications in patients with sporadic CC-RCC. Patients who underwent nephrectomy were eligible if they had pathologically confirmed CC-RCC not associated with VHL disease or familial RCC. Tumor tissues were selected from paraffin blocks on the basis of hematoxylin and eosin (H&E)-stained sections. Polymerase chain reaction-single strand conformation polymorphism analysis was performed to detect VHL mutations and genetic changes in HIF-1alpha, which were followed by automated direct sequencing. VHL hypermethylation was examined by methylation-specific PCR. A total of 56 patients were enrolled and somatic VHL alterations were detected in 16 patients (29%); intragenic mutation in eight, hypermethylation in five, both alterations in three. The mutation types were missense in five patients, silent in three, nonsense in two, and frameshift in one. Somatic VHL alterations were not significantly associated with progression-free survival (PFS) or overall survival (OS). However, patients with 'loss-of-function' VHL mutation showed significantly decreased PFS (P=0.016) and OS (P=0.046). Although the association between VHL alteration and response to immunotherapy was not significant (P=0.486), patients with missense mutation seem to have better response to immunotherapy. The Pro582Ser change in HIF-1alpha was detected in six patients (11%) and was positively correlated with the development of metastases (P=0.023). This study did not show an association between somatic VHL alteration and prognosis in patients with sporadic CC-RCC. However, it suggests that the therapeutic and prognostic implication of somatic VHL alteration may be different according to the mutational subtype and that the Pro582Ser change in HIF-1alpha may contribute to the development of metastases.

摘要

冯·希佩尔-林道(VHL)基因的体细胞失活是在透明细胞肾细胞癌(CC-RCC)中观察到的最常见的基因事件。然而,体细胞VHL改变及其靶点缺氧诱导因子(HIF)-1α的预后相关性尚未明确。我们研究了VHL基因和HIF-1α的基因变化,并探讨了它们在散发性CC-RCC患者中的临床意义。接受肾切除术的患者,如果其病理确诊为CC-RCC且与VHL病或家族性RCC无关,则符合入选标准。根据苏木精和伊红(H&E)染色切片从石蜡块中选取肿瘤组织。进行聚合酶链反应-单链构象多态性分析以检测VHL突变和HIF-1α的基因变化,随后进行自动直接测序。通过甲基化特异性PCR检测VHL高甲基化。共纳入56例患者,16例患者(29%)检测到体细胞VHL改变;8例为基因内突变,5例为高甲基化,3例同时存在两种改变。突变类型中,5例为错义突变,3例为沉默突变,2例为无义突变,1例为移码突变。体细胞VHL改变与无进展生存期(PFS)或总生存期(OS)无显著相关性。然而,具有“功能丧失”VHL突变的患者PFS(P=0.016)和OS(P=0.046)显著降低。虽然VHL改变与免疫治疗反应之间的相关性不显著(P=0.486),但错义突变患者似乎对免疫治疗反应更好。在6例患者(11%)中检测到HIF-1α的Pro582Ser改变,且与转移的发生呈正相关(P=0.023)。本研究未显示散发性CC-RCC患者体细胞VHL改变与预后之间存在关联。然而,这表明体细胞VHL改变的治疗和预后意义可能因突变亚型而异,且HIF-1α的Pro582Ser改变可能促进转移的发生。

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