Department of Pathophysiology, Laboratory for Stem Cell and Tissue Engineering, Chongqing Medical University, Chongqing 400016, China.
Chin J Cancer Res. 2012 Sep;24(3):213-9. doi: 10.1007/s11670-012-0213-9.
To investigate the effects and mechanisms of trastuzumab on Notch-1 pathway in breast cancer cells, recognizing the significance of Notch-1 signaling pathway in trastuzumab resistance.
Immunocytochemistry staining and Western blotting were employed to justify the expression of Notch-1 protein in HER2-overexpressing SK-BR3 cells and HER2-non-overexpressing breast cancer MDA-MB-231 cells. Western blotting and reverse transcription PCR (RT-PCR) were used to detect the activated Notch-1 and Notch-1 target gene HES-1 mRNA expression after SK-BR3 cells were treated with trastuzumab. Double immunofluorescence staining and co-immunoprecipitation were used to analyze the relationship of Notch-1 and HER2 proteins.
The level of Notch-1 nuclear localization and activated Notch-1 proteins in HER2-overexpressing cells were significantly lower than in HER2-non-overexpressing cells (P<0.01), and the expressions of activated Notch-1 and HES-1 mRNA were obviously increased after trastuzumab treatment (P<0.05), but HER2 expression did not change significantly for trastuzumab treating (P>0.05). Moreover, Notch-1 was discovered to co-localize and interact with HER2 in SK-BR3 cells.
Overexpression of HER2 decreased Notch-1 activity by the formation of a HER2-Notch1 complex, and trastuzumab can restore the activity of Notch-1 signaling pathway, which could be associated with cell resistance to trastuzumab.
研究曲妥珠单抗对乳腺癌细胞 Notch-1 通路的作用及其机制,认识 Notch-1 信号通路在曲妥珠单抗耐药中的意义。
采用免疫细胞化学染色和 Western blot 法验证曲妥珠单抗耐药的人表皮生长因子受体 2(HER2)过表达 SK-BR3 细胞和 HER2 非过表达乳腺癌 MDA-MB-231 细胞中 Notch-1 蛋白的表达。Western blot 和逆转录聚合酶链反应(RT-PCR)检测 SK-BR3 细胞经曲妥珠单抗处理后激活的 Notch-1 及其靶基因 HES-1mRNA 的表达。双免疫荧光染色和免疫共沉淀分析 Notch-1 与 HER2 蛋白的关系。
HER2 过表达细胞 Notch-1 核内定位和激活型 Notch-1 蛋白水平明显低于 HER2 非过表达细胞(P<0.01),曲妥珠单抗处理后激活型 Notch-1 和 HES-1mRNA 的表达明显增加(P<0.05),但 HER2 表达无明显变化(P>0.05)。此外,在 SK-BR3 细胞中发现 Notch-1 与 HER2 共定位并相互作用。
HER2 的过表达通过形成 HER2-Notch1 复合物降低 Notch-1 的活性,曲妥珠单抗可恢复 Notch-1 信号通路的活性,这可能与细胞对曲妥珠单抗的耐药性有关。