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痣样基底细胞癌综合征患者PTCH基因第17外显子突变分析。

Analysis of mutation in exon 17 of PTCH in patients with nevoid basal cell carcinoma syndrome.

作者信息

Li Jichen, Wang Jinhui, Liu Yingqun, Wang Wei

机构信息

Department of Oral Maxillofacial Surgery, School of Stomatology, Harbin Medical University, Harbin, China.

出版信息

Mol Biol Rep. 2010 Jan;37(1):359-62. doi: 10.1007/s11033-009-9782-1.

Abstract

Abnormalities in sonic hedgehog (SHH) signaling pathway components are major contributing factors in the development of nevoid basal cell carcinoma syndromes (NBCCS) that include SHH, PTCH, SMO and GLI. The novel patched homologue (PTCH) mutation and clinical manifestations with NBCCS links PTCH haplosufficiency and aberrant activation of the sonic hedgehog/Patched/smoothened pathway. To investigate further the molecular genetics of NBCCS, we performed mutation analysis of PTCH gene in a family case with five affected members. These clinical manifestations might be associated with a novel constitutional mutation of the PTCH gene, 3146A-->T (1049N-->I), in exon 17. The analyzed results of tumor tissue show a high expression of GLI. Our findings suggested that the mutation of 3146A-->T may be the cause of high expression of GLI and permit SMO to transmit signal to the nucleus through SHH/PTCH/SMO pathway.

摘要

音猬因子(SHH)信号通路成分异常是痣样基底细胞癌综合征(NBCCS)发生发展的主要因素,该综合征包括SHH、PTCH、SMO和GLI。新型patched同源物(PTCH)突变及NBCCS的临床表现将PTCH单倍剂量不足与音猬因子/Patched/ smoothened通路的异常激活联系起来。为进一步研究NBCCS的分子遗传学,我们对一个有5名患病成员的家族病例进行了PTCH基因突变分析。这些临床表现可能与第17外显子中PTCH基因的一种新的胚系突变3146A→T(1049N→I)有关。肿瘤组织的分析结果显示GLI高表达。我们的研究结果表明,3146A→T突变可能是GLI高表达的原因,并使SMO能够通过SHH/PTCH/SMO通路将信号传递至细胞核。

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