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LKB1 突变在黏液性细支气管肺泡癌中经常被检测到。

LKB1 mutations frequently detected in mucinous bronchioloalveolar carcinoma.

机构信息

Department of Thoracic Oncology, National Kyushu Cancer Center, Notame 3-1-1, Minami-ku, Fukuoka 811-1395, Japan.

出版信息

Jpn J Clin Oncol. 2011 Sep;41(9):1132-7. doi: 10.1093/jjco/hyr102. Epub 2011 Aug 4.

Abstract

OBJECTIVE

LKB1 mutations are common in patients with Peutz-Jeghers syndrome, which is characterized by mucocutaneous pigmentation, intestinal polyps and a high incidence of cancers at variable sites. This study investigated the status of the LKB1 gene in mucinous bronchioloalveolar carcinoma with or without Peutz-Jeghers syndrome.

METHODS

Three mucinous bronchioloalveolar carcinoma tumors from two Peutz-Jeghers syndrome patients and seven tumors from sporadic mucinous bronchioloalveolar carcinoma patients were collected by surgery between 2002 and 2008, and high molecular weight genomic DNA was extracted from them. The nucleotide sequences in exons 1-9 of LKB1 were determined by genomic polymerase chain reaction-direct sequencing. The loss of heterozygosity was analyzed by high-resolution fluorescent microsatellite analysis using two microsatellite markers that encompass the LKB1 locus, D19S886 and D19S565. The mutations of KRAS, EGFR and p53 were also evaluated.

RESULTS

The germline mutation of LKB1 in the Peutz-Jeghers syndrome patients was identified as G215D by analyzing genomic DNA from normal lung tissue specimens. Furthermore, two of the three mucinous bronchioloalveolar carcinomas from these Peutz-Jeghers syndrome patients exhibited additional somatic mutations. On the other hand, four of seven sporadic 'non-Peutz-Jeghers syndrome' mucinous bronchioloalveolar carcinomas had LKB1 mutations. Loss of heterozygosity analyses revealed allelic loss in two tumors with LKB1 mutations. As a result, 70% of the mucinous bronchioloalveolar carcinomas exhibited LKB1 mutations. KRAS, EGFR and p53 mutations were mutually exclusive and observed in four, two and one tumors, respectively. Among them, five mutations occurred concomitantly with LKB1 mutations.

CONCLUSIONS

The relatively high frequency of LKB1 mutations in mucinous bronchioloalveolar carcinoma patients may therefore suggest its involvement in lung carcinogenesis, at least in mucinous bronchioloalveolar carcinoma.

摘要

目的

LKB1 基因突变常见于 Peutz-Jeghers 综合征患者,该综合征的特征是黏膜皮肤色素沉着、肠息肉和不同部位癌症的高发生率。本研究调查了伴有或不伴有 Peutz-Jeghers 综合征的黏液性细支气管肺泡癌中 LKB1 基因的状态。

方法

本研究于 2002 年至 2008 年间通过手术收集了两名 Peutz-Jeghers 综合征患者的 3 个黏液性细支气管肺泡癌肿瘤和 7 个散发性黏液性细支气管肺泡癌肿瘤,并从中提取高分子量基因组 DNA。通过基因组聚合酶链反应直接测序确定 LKB1 外显子 1-9 的核苷酸序列。使用包含 LKB1 基因座的两个微卫星标记 D19S886 和 D19S565 进行高分辨率荧光微卫星分析,以分析杂合性缺失。还评估了 KRAS、EGFR 和 p53 的突变情况。

结果

通过分析正常肺组织标本中的基因组 DNA,在 Peutz-Jeghers 综合征患者中鉴定出 LKB1 的种系突变 G215D。此外,这两名患者的 3 个黏液性细支气管肺泡癌中的 2 个还表现出额外的体细胞突变。另一方面,7 个散发性“非 Peutz-Jeghers 综合征”黏液性细支气管肺泡癌中有 4 个存在 LKB1 突变。杂合性缺失分析显示,在两个具有 LKB1 突变的肿瘤中存在等位基因丢失。因此,70%的黏液性细支气管肺泡癌存在 LKB1 突变。KRAS、EGFR 和 p53 突变是相互排斥的,分别在 4、2 和 1 个肿瘤中观察到。其中,5 个突变与 LKB1 突变同时发生。

结论

黏液性细支气管肺泡癌患者中 LKB1 突变的相对较高频率可能提示其参与了肺癌的发生,至少在黏液性细支气管肺泡癌中是这样。

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