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Comprehensive Analysis of ERK1/2 Substrates for Potential Combination Immunotherapies

机译:ERK1 / 2底物综合分析潜在组合免疫疗法

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摘要

Recent clinical and therapeutic success with RAF and MEK1/2 inhibitors has revolutionized the existing treatment schemes for previously incurable cancers like melanomas. However, the overall therapeutic efficacies are still largely compromised by the dose-limiting side effects and emerging drug resistance mechanisms. Accumulating evidence has revealed the intricate nature of the RAS-RAF-MEK1/2-ERK1/2 pathway, such as activation mechanisms, kinase-substrate relationships, crosstalk with parallel signaling pathways, feedback regulations, and intimate interplay with immune responses. Limited strategies are currently available to exploit the benefits of combining RAF-MEK1/2-ERK1/2 pathway inhibitors with other targeted therapies or immunotherapies. Here, we compiled the kinase-substrate relationships and analyzed the intricate signaling networks of the renowned pathway, providing an integrated and simplified visualization, to reveal the potentials of RAS-RAF-MEK1/2-ERK1/2-based combination therapies.
机译:近期与RAF和MEK1 / 2抑制剂的临床和治疗成功彻底改变了现有的Melanomas等癌症的现有治疗方案。然而,整体治疗效率仍然受到剂量限制副作用和新出现的耐药机制的影响。累积证据揭示了Ras-Raf-Mek1 / 2-ERK1 / 2途径的复杂性,例如活化机制,激酶 - 底物关系,具有平行信号通路,反馈规定和具有免疫反应的亲密相互作用的串扰性。目前可用于利用Raf-Mek1 / 2-ERK1 / 2途径抑制剂与其他有针对性疗法或免疫治疗的益处有限。在这里,我们编译了激酶底物关系并分析了着名途径的复杂信号网络,提供了集成和简化的可视化,以揭示基于RAS-RAF-MEK1 / 2-ERK1 / 2的组合疗法的电位。

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  • 来源
    《Trends in pharmacological sciences》 |2019年第11期|共14页
  • 作者单位

    Natl Univ Singapore Dept Biol Sci Singapore 117543 Singapore;

    Nanyang Technol Univ Sch Biol Sci Singapore 637551 Singapore;

    Natl Univ Singapore Ctr Translat Med Canc Sci Inst Singapore 14 Med Dr 12-01 Singapore 117599;

    Natl Univ Singapore Dept Biol Sci Singapore 117543 Singapore;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 药理学;
  • 关键词

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