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肺对侧细支气管肺泡癌的基因改变

Genetic changes in contralateral bronchioloalveolar carcinomas of the lung.

作者信息

Shin S W, Breathnach O S, Linnoila R I, Williams J, Gillespie J W, Kelley M J, Johnson B E

机构信息

Medicine Branch, Division of Clinical Sciences, National Cancer Institute, Bethesda, Md., USA.

出版信息

Oncology. 2001;60(1):81-7. doi: 10.1159/000055301.

Abstract

OBJECTIVE

The pattern of metastases and recurrence of bronchioloalveolar carcinoma (BAC) differs from adenocarcinoma of the lung, occurring more frequently within the lung without extrapulmonary involvement. Analyses of genetic differences of contralateral BACs may help to explain these clinical differences.

METHODS

We compared paired tumors from 5 patients with contralateral metachronous BACs for loss of heterozygosity (LOH) on 6 chromosomal arms (2q, 3p, 5q, 9p, 13q and 17p) and mutational analysis of p53 and K-ras.

RESULTS

Two patients, patients 1 and 2, had discordant patterns of LOH on 2 and 3 of the chromosome arms, respectively. In addition, patient 2 had a detectable K-ras mutation in his initial tumor but not in his second. These results suggest that in patients 1 and 2, the contralateral tumors were clonally unrelated. Patient 3 had no mutations in the K-ras or p53 gene and no LOH on any of the 5 informative chromosome arms. Patient 4 had LOH of 9p and mutated K-ras in both the first and the second tumor, with a mutation in the p53 gene in the first but not in the second tumor. Patient 5 had LOH of 17p and the same p53 mutations in both the first and the second tumor, with a mutation of K-ras in the first tumor but not in the second.

CONCLUSIONS

The preponderance of evidence suggests that in patients 3, 4 and 5, the paired tumors were clonally related. The different patterns of LOH and mutations in clinically similar contralateral metachronous BACs provide evidence of genetic heterogeneity in the tumors of this patient group.

摘要

目的

细支气管肺泡癌(BAC)的转移和复发模式与肺腺癌不同,其在肺内发生更为频繁,无肺外受累。对双侧BACs的基因差异进行分析可能有助于解释这些临床差异。

方法

我们比较了5例双侧异时性BACs患者的配对肿瘤,分析其6条染色体臂(2q、3p、5q、9p、13q和17p)上的杂合性缺失(LOH)以及p53和K-ras的突变情况。

结果

患者1和患者2这两名患者在2条和3条染色体臂上分别出现了不一致的LOH模式。此外,患者2在其初始肿瘤中检测到K-ras突变,而在第二个肿瘤中未检测到。这些结果表明,患者1和患者2的双侧肿瘤在克隆上不相关。患者3的K-ras或p53基因无突变,在5条有信息的染色体臂上均无LOH。患者4的第一个和第二个肿瘤均有9p的LOH和K-ras突变,第一个肿瘤中有p53基因突变,第二个肿瘤中无。患者5的第一个和第二个肿瘤均有17p的LOH和相同的p53突变,第一个肿瘤中有K-ras突变,第二个肿瘤中无。

结论

大量证据表明,患者3、4和5的配对肿瘤在克隆上相关。临床相似的双侧异时性BACs中不同的LOH和突变模式为该患者组肿瘤的基因异质性提供了证据。

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