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首页> 外文期刊>Cancer letters >CXCR4 suppression attenuates EGFRvIII-mediated invasion and induces p38 MAPK-dependent protein trafficking and degradation of EGFRvIII in breast cancer cells.
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CXCR4 suppression attenuates EGFRvIII-mediated invasion and induces p38 MAPK-dependent protein trafficking and degradation of EGFRvIII in breast cancer cells.

机译:CXCR4抑制作用减弱了EGFRvIII介导的侵袭,并诱导了乳腺癌细胞中p38 MAPK依赖性蛋白的运输和EGFRvIII的降解。

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摘要

Our previous report has shown that the constitutively activated EGFR variant, EGFRvIII, up-regulates the pro-metastatic chemokine receptor CXCR4 in breast cancer cells. Here we evaluated the biological effect and cell signaling effects of silencing CXCR4 expression in EGFRvIII-expressing breast cancer cells. Short hairpin RNA (shRNA)-mediated suppression of CXCR4 expression significantly reduced the invasive potential and proliferation of EGFRvIII-expressing breast cancer cells. These cells exhibited a reduction of EGFRvIII activity and protein expression due to increased protein degradation and altered protein trafficking. In conclusion, suppression of CXCR4 inhibits EGFRvIII-mediated breast cancer cell invasion and proliferation.
机译:我们以前的报告表明,组成型激活的EGFR变体EGFRvIII上调了乳腺癌细胞中促转移趋化因子受体CXCR4的表达。在这里,我们评估了表达EGFRvIII的乳腺癌细胞中沉默CXCR4表达的生物学效应和细胞信号传导效应。短发夹RNA(shRNA)介导的对CXCR4表达的抑制显着降低了表达EGFRvIII的乳腺癌细胞的侵袭潜力和增殖。由于增加的蛋白质降解和改变的蛋白质运输,这些细胞表现出EGFRvIII活性和蛋白质表达的降低。总之,抑制CXCR4可抑制EGFRvIII介导的乳腺癌细胞的侵袭和增殖。

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