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What a Tangled Web We Weave: Emerging Resistance Mechanisms to Inhibition of the Phosphoinositide 3-kinase Pathway

机译:我们编织了什么纠结的网:新兴的抗磷脂酰肌醇3-激酶途径抑制机制。

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摘要

The phosphoinositide 3-kinase (PI3K) pathway is one of the most frequently mutated pathways in cancer, and is actively being pursued as a therapeutic target. Despite the importance of the PI3K pathway in cancer, durable responses to PI3K-pathway targeted therapies are uncommon with monotherapy. Several in vitro and xenograft models have elucidated compensatory signaling and genomic changes which may limit the therapeutic effectiveness of PI3K inhibitors in the clinic. Future clinical trials with prospective evaluation of tumor signaling and genomic changes are likely to identify novel resistance mechanisms as well as subsets of patients who may derive maximal benefit from PI3K pathway inhibitors.
机译:磷酸肌醇3-激酶(PI3K)途径是癌症中最常见的突变途径之一,并且正在积极地追求作为治疗靶标。尽管PI3K途径在癌症中具有重要意义,但对PI3K途径靶向治疗的持久反应在单药治疗中并不常见。几种体外和异种移植模型已经阐明了补偿信号传导和基因组变化,这可能会限制PI3K抑制剂在临床上的治疗效果。未来对肿瘤信号传导和基因组变化进行前瞻性评估的临床试验可能会确定出新的耐药机制,以及可能从PI3K途径抑制剂中获得最大收益的患者子集。

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