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Wilms 瘤 1 异构体与 HER2 和 ER-α 的相关性及其在乳腺癌中的致癌作用。

Correlation of Wilms' tumor 1 isoforms with HER2 and ER-α and its oncogenic role in breast cancer.

机构信息

Department of Biomedical Sciences, Faculty of Medicine, Prince of Songkla University, Hat-Yai, Songkhla, 90110, Thailand.

出版信息

Anticancer Res. 2014 Mar;34(3):1333-42.

Abstract

BACKGROUND

Wilms' tumor 1 (WT1) gene has different functional properties depending on the isoform type. This gene correlates with cell proliferation in various types of cancer. Here, we investigated the expression of WT1 isoforms in breast cancer tissues, and focused on the oncogenic role through estrogen receptor-alpha (ER-α) and human epidermal growth factor receptor 2 (HER2).

MATERIALS AND METHODS

Expression of WT1(17AA+) and (17AA-) was investigated in adjacent normal breast and breast cancer using Reverse transcription-polymerase chain reaction and western blotting. The correlation of WT1 isoforms with HER2 and ER-α was examined using MCF-7 cells stably-overexpressing WT1s and siRNA against WT1 gene.

RESULTS

The expression of WT(17AA-) was significantly found in adjacent normal breast tissues. A mixture of WT1(17AA+) and WT1(17AA-) were highly expressed in breast carcinoma tissues. MCF-7 cells overexpressing WT1+/+ and WT1+/- represented strong expression of ER-α and HER2. Moreover, the silencing of WT1+/+ and WT1+/- resulted in a decrease of both ER-α and HER2 and led to a decrease of cell numbers.

CONCLUSION

Our results suggest that WT1(17AA+) was exhibited dominantly in breast carcinoma tissues. WT1+/+ and WT1+/- correlated with the high expression of ER-α and HER2, leading to cell proliferation and might be involved in cancer development and progression.

摘要

背景

Wilms 瘤 1(WT1)基因具有不同的功能特性,取决于异构体类型。该基因与多种类型癌症中的细胞增殖相关。在这里,我们研究了乳腺癌组织中 WT1 异构体的表达,并通过雌激素受体-α(ER-α)和人表皮生长因子受体 2(HER2)聚焦其致癌作用。

材料和方法

使用逆转录聚合酶链反应和 Western blot 法检测相邻正常乳腺和乳腺癌中 WT1(17AA+)和(17AA-)的表达。使用 MCF-7 细胞中稳定过表达 WT1s 和针对 WT1 基因的 siRNA 检测 WT1 异构体与 HER2 和 ER-α 的相关性。

结果

WT(17AA-)在相邻正常乳腺组织中表达明显。WT1(17AA+)和 WT1(17AA-)的混合物在乳腺癌组织中高度表达。过表达 WT1+/+和 WT1+/-的 MCF-7 细胞表现出强烈的 ER-α 和 HER2 表达。此外,WT1+/+和 WT1+/-的沉默导致 ER-α 和 HER2 的表达降低,导致细胞数量减少。

结论

我们的结果表明,WT1(17AA+)在乳腺癌组织中表现出优势表达。WT1+/+和 WT1+/-与 ER-α 和 HER2 的高表达相关,导致细胞增殖,可能参与癌症的发生和发展。

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