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The FAK inhibitor BI 853520 exerts anti-tumor effects in breast cancer

机译:FAK抑制剂BI 853520在乳腺癌中发挥抗肿瘤作用

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Focal adhesion kinase (FAK) is a cytoplasmic tyrosine kinase that regulates a plethora of downstream signaling pathways essential for cell migration, proliferation and death, processes that are exploited by cancer cells during malignant progression. These well-established tumorigenic activities, together with its high expression and activity in different cancer types, highlight FAK as an attractive target for cancer therapy. We have assessed and characterized the therapeutic potential and the biological effects of BI 853520, a novel small chemical inhibitor of FAK, in several preclinical mouse models of breast cancer. Treatment with BI 853520 elicits a significant reduction in primary tumor growth caused by an anti-proliferative activity by BI 853520. In contrast, BI 853520 exerts effects with varying degrees of robustness on the different stages of the metastatic cascade. Together, the data demonstrate that the repression of FAK activity by the specific FAK inhibitor BI 853520 offers a promising anti-proliferative approach for cancer therapy.
机译:粘着斑激酶(FAK)是一种细胞质酪氨酸激酶,可调节过多的下游信号通路,这些信号通路对于癌细胞迁移,增殖和死亡至关重要,而癌细胞在恶性进展过程中会利用这些信号通路。这些公认的致癌活性,以及​​其在不同癌症类型中的高表达和活性,突出了FAK作为癌症治疗的诱人靶标。我们已经评估和表征了BI 853520(一种新型的FAK小化学抑制剂)在几种乳腺癌的临床前小鼠模型中的治疗潜力和生物学作用。 BI 853520的治疗引起BI 853520的抗增殖活性引起的原发肿瘤生长显着减少。相反,BI 853520对转移级联反应的不同阶段具有不同程度的稳健性。总之,数据表明,特定的FAK抑制剂BI 853520对FAK活性的抑制为癌症治疗提供了一种有希望的抗增殖方法。

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