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AID 在人肺癌中的异常表达和致突变活性。

Aberrant expression and mutation-inducing activity of AID in human lung cancer.

机构信息

Department of Pathology, Hamamatsu University School of Medicine, Hamamatsu, Japan.

出版信息

Ann Surg Oncol. 2011 Jul;18(7):2084-92. doi: 10.1245/s10434-011-1568-8. Epub 2011 Feb 3.

Abstract

BACKGROUND

Activation-induced cytidine deaminase (AID) is expressed in B lymphocytes and triggers antibody diversification. Recent reports have indicated that the constitutive expression of AID in mice causes not only lymphomas, but also cancers of some organs including the lung, prompting us to investigate the expression and effect of AID on human lung cancer.

MATERIALS AND METHODS

We examined AID mRNA expression in 17 lung cancer cell lines and 51 primary lung cancers using a quantitative RT-PCR analysis. Next, we established H1299 lung cancer cells stably overexpressing AID and performed a supF forward mutation assay. We then examined AID protein expression and p53 mutation in 129 primary lung cancers by an immunohistochemical analysis and PCR-SSCP and sequencing analyses, respectively.

RESULTS

Aberrant mRNA expression of AID was detected in 29% (5 of 17) of the lung cancer cell lines and 31% (16 of 51) of the primary lung cancers. AID-overexpressing H1299 clones showed a 5.0- to 6.1-fold higher mutation frequency than an empty vector-transfected H1299 clone, and about half of the AID-induced mutations were base substitutions, indicating that AID induces gene mutations in lung cancer cells. Furthermore, an association was found between the AID protein expression level and the p53 mutation status in an analysis of 129 primary lung cancers. A further expression analysis revealed that a portion of AID is localized at the centrosomes.

CONCLUSION

Our current findings suggest that the aberrant expression of AID may be involved in a subset of human lung cancers as a result of its mutation-inducing activity.

摘要

背景

激活诱导胞嘧啶脱氨酶(AID)在 B 淋巴细胞中表达,触发抗体多样化。最近的报告表明,AID 在小鼠中的组成型表达不仅会导致淋巴瘤,还会导致包括肺在内的一些器官的癌症,这促使我们研究 AID 对人类肺癌的表达和影响。

材料和方法

我们使用定量 RT-PCR 分析检查了 17 种肺癌细胞系和 51 种原发性肺癌中 AID mRNA 的表达。接下来,我们建立了稳定过表达 AID 的 H1299 肺癌细胞,并进行了 supF 正向突变测定。然后,我们通过免疫组织化学分析和 PCR-SSCP 及测序分析,分别检测了 129 例原发性肺癌中的 AID 蛋白表达和 p53 突变。

结果

在 29%(17 个细胞系中的 5 个)的肺癌细胞系和 31%(51 个原发性肺癌中的 16 个)中检测到 AID 异常 mRNA 表达。与空载体转染的 H1299 克隆相比,过表达 AID 的 H1299 克隆的突变频率高出 5.0-6.1 倍,并且大约一半的 AID 诱导的突变是碱基替换,表明 AID 诱导肺癌细胞中的基因突变。此外,在对 129 例原发性肺癌的分析中,发现 AID 蛋白表达水平与 p53 突变状态之间存在关联。进一步的表达分析表明,一部分 AID 定位于中心体。

结论

我们目前的研究结果表明,由于其诱导突变的活性,AID 的异常表达可能参与了一部分人类肺癌的发生。

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