Oncogenesis:伊马替尼或可靶向治疗某些雌激素受体阳性乳腺小叶浸润癌

2018-02-14 Aries 肿瘤资讯

该研究使用新的雌激素受体阳性ILC模型(BCK4)和基因表达阵列发现,BCK4细胞系和异种移植肿瘤大约200个重叠基因受到体外雌激素调节,根据通路分析显示,c-Kit通路可能成为减少雌激素诱导乳腺癌细胞增殖的靶点。

该研究使用新的雌激素受体阳性ILC模型(BCK4)和基因表达阵列发现,BCK4细胞系和异种移植肿瘤大约200个重叠基因受到体外雌激素调节,根据通路分析显示,c-Kit通路可能成为减少雌激素诱导乳腺癌细胞增殖的靶点。该研究还发现,用于治疗白血病的甲磺酸伊马替尼(格列卫)能够抑制c-Kit活性,与雌激素受体拮抗剂氟维司群(芙仕得)可以同样有效阻断雌激素对体外BCK4细胞和BCK4肿瘤的刺激。此外,使用小发夹核糖核酸(shRNA)干扰c-Kit表达,也可减少基线和雌激素诱导的体外和体内乳腺癌细胞增殖。因此,该研究首次表明,抑制c-Kit或可成为靶向治疗c-Kit阳性ILC的有效方法。

原始出处:

J. Chuck Harrell, Thomas M. Shroka,Britta M. Jacobsen.Estrogen induces c-Kit and an aggressive phenotype in a model of invasive lobular breast cancer.Oncogenesis.27 November 2017

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    2018-05-13 cy0324
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    2018-02-16 zsyan
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    2018-02-16 skhzy
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    2018-02-14 1e145228m78(暂无匿称)

    学习了.谢谢作者分享!

    0