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首页> 外文期刊>Journal of Cancer >Comprehensive Two- and Three-Dimensional RNAi Screening Identifies PI3K Inhibition as a Complement to MEK Inhibitor AS703026 for Combination Treatment of Triple-Negative Breast Cancer
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Comprehensive Two- and Three-Dimensional RNAi Screening Identifies PI3K Inhibition as a Complement to MEK Inhibitor AS703026 for Combination Treatment of Triple-Negative Breast Cancer

机译:全面的二维和三维RNAi筛选可确定PI3K抑制是MEK抑制剂AS703026的补充,用于三阴性乳腺癌的联合治疗。

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Triple-negative breast cancer (TNBC) is a major cause of death among breast cancer patients that results from intrinsic and acquired resistance to systemic chemotherapies. To identify novel targets for effective treatment of TNBC through combination strategies with MEK inhibitor (AS703026), we used a novel method of combining high-throughput two- and three-dimensional (2D and 3D) RNAi screening. TNBC cells were transfected with a kinome siRNA library comprising siRNA targeting 790 kinases under both 2D and 3D culture conditions with or without AS703026. Molecule activity predictor analysis revealed the PI3K pathway as the major target pathway in our RNAi combination studies in TNBC. We found that PI3K inhibitor SAR245409 (also called XL765) combined with AS703026 synergistically inhibited proliferation compared with either drug alone (P in vitro colony formation (P in vitro and in vivo culture conditions, and enriches targets that are close to the in vivo condition.
机译:三阴性乳腺癌(TNBC)是乳腺癌患者死亡的主要原因,其原因是对系统化学疗法的内在和获得性抵抗。为了通过MEK抑制剂(AS703026)的联合策略确定有效治疗TNBC的新靶标,我们使用了结合高通量二维和三维(2D和3D)RNAi筛选的新方法。在包含或不包含AS703026的2D和3D培养条件下,用包含靶向790激酶的siRNA的kinome siRNA文库转染TNBC细胞。分子活性预测因子分析显示,在我们在TNBC的RNAi组合研究中,PI3K途径是主要的靶途径。我们发现PI3K抑制剂SAR245409(也称为XL765)与AS703026联合使用与单独使用任一药物(P体外菌落形成(P体外和体内培养条件,并富集了接近体内条件的靶标))相比均能协同抑制增殖。

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