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伴有微卫星不稳定的人子宫内膜癌中的Birt-Hogg-Dubé基因突变

Birt-Hogg-Dubé gene mutations in human endometrial carcinomas with microsatellite instability.

作者信息

Fujii H, Jiang W, Matsumoto T, Miyai K, Sashara K, Ohtsuji N, Hino O

机构信息

Department of Pathology II, Juntendo University School of Medicine, Tokyo, 113-8421 Japan.

出版信息

J Pathol. 2006 Jul;209(3):328-35. doi: 10.1002/path.1992.

Abstract

Birt-Hogg-Dubé (BHD) syndrome is a rare form of autosomal dominantly inherited genodermatosis characterized by benign hamartomatous skin lesions named fibrofolliculomas, and an increased risk for developing pulmonary cyst/pneumothorax and various forms of renal cell carcinoma. Many of the patients harbour insertion/deletion mutations in the hypermutable poly(C)8 tract in exon 11 of the BHD gene. This mutational hot spot is also reported to be a target of mutation in microsatellite instability (MSI) sporadic colorectal cancer. To test the hypothesis that the BHD gene is also a mutational target in sporadic endometrial carcinoma with microsatellite instability, 139 cases of sporadic endometrial carcinoma were screened for MSI status, and mutations of the poly(C)8 tract in exon 11 as well as other coding exons of the BHD gene. The poly(G)8 tract of the BAX gene, the poly(C)8 tract of MSH6, and methylation status of hMLH1 were also assessed. Thirty-nine of 139 cases (28%) showed MSI. Mutations in the poly(C)8 tract of BHD were detected in five of the 39 MSI cases (12.8%). Of these, one showed additional mutation in exon 4, possibly satisfying the two-hit hypothesis of tumour suppressor genes. BAX gene mutation was detected in ten of the 39 MSI cases (25.6%). Four tumours showed both BAX and BHD mutations, and a significant positive association was found between mutations of the two genes. No association was found between BHD status and MSH6 mutation or hMLH1 methylation. When multiple foci were microdissected and individually screened for mutation, BHD mutations were shown to have been acquired during tumour progression, after mutation of the BAX gene, in three of five cases. Taken together, these findings show that the BHD gene is a target gene in MSI endometrial carcinoma. However, its mutational frequency is lower than that of BAX, and BHD mutation tends to occur during neoplastic progression after the acquisition of mutations in another MSI target gene, BAX.

摘要

Birt-Hogg-Dubé(BHD)综合征是一种罕见的常染色体显性遗传的遗传性皮肤病,其特征为存在名为纤维毛囊瘤的良性错构瘤性皮肤病变,以及发生肺囊肿/气胸和各种形式肾细胞癌的风险增加。许多患者在BHD基因第11外显子的高度可变的聚(C)8序列中存在插入/缺失突变。据报道,这个突变热点也是微卫星不稳定性(MSI)散发性结直肠癌的突变靶点。为了验证BHD基因也是具有微卫星不稳定性的散发性子宫内膜癌的突变靶点这一假说,对139例散发性子宫内膜癌病例进行了MSI状态筛查,以及BHD基因第11外显子聚(C)8序列和其他编码外显子的突变检测。还评估了BAX基因的聚(G)8序列、MSH6的聚(C)8序列以及hMLH1的甲基化状态。139例病例中有39例(28%)显示为MSI。在39例MSI病例中有5例(12.8%)检测到BHD基因聚(C)8序列突变。其中,1例在第4外显子中还存在额外突变,可能符合肿瘤抑制基因的双打击假说。在39例MSI病例中有10例(25.6%)检测到BAX基因突变。4个肿瘤同时存在BAX和BHD突变,并且发现这两个基因的突变之间存在显著正相关。未发现BHD状态与MSH6突变或hMLH1甲基化之间存在关联。当对多个病灶进行显微切割并分别筛查突变时,在5例中的3例中显示BHD突变是在肿瘤进展过程中、在BAX基因突变之后获得的。综上所述,这些发现表明BHD基因是MSI子宫内膜癌中的一个靶基因。然而,其突变频率低于BAX,并且BHD突变倾向于在另一个MSI靶基因BAX发生突变之后的肿瘤进展过程中出现。

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