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在癌症治疗的早期临床试验中,研究性 IGF1R 抑制剂。

Investigational IGF1R inhibitors in early stage clinical trials for cancer therapy.

机构信息

Department of Human Molecular Genetics and Biochemistry, Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.

Yoran Institute for Human Genome Research, Tel Aviv University, Tel Aviv, Israel.

出版信息

Expert Opin Investig Drugs. 2019 Dec;28(12):1101-1112. doi: 10.1080/13543784.2019.1694660. Epub 2019 Nov 23.

Abstract

: The insulin-like growth factors (IGFs) are a family of secreted peptide hormones with important roles in different cellular and organism functions. The biological activities of the IGFs are mediated by the IGF1 receptor (IGF1R), a cell surface, tyrosine kinase-containing heterotetramer that is linked to numerous cytoplasmic signaling cascades. The IGF1R displays potent antiapoptotic, pro-survival capacities and plays a key role in malignant transformation. Research has identified the IGF1R as a candidate therapeutic target in cancer.: We offer a synopsis of ongoing efforts to target the IGF axis for therapeutic purposes. Our review includes a digest of early experimental work that led to the identification of IGF1R as a candidate therapeutic target in oncology.: Targeting of the IGF axis has yielded disappointing results in phase III trials, but it is important to learn from this to improve future trials in a rational manner. The potential of anti-IGF1R antibodies and small molecular weight inhibitors, alone or in combination with chemotherapy or other biological agents, should be investigated further in randomized studies. Moreover, the implementation of predictive biomarkers for patient selection will improve the outcome of future trials. Emerging personalized medicine could have a major impact on IGF1R targeting.

摘要

胰岛素样生长因子 (IGFs) 是一组分泌的肽类激素,在不同的细胞和机体功能中具有重要作用。IGFs 的生物学活性由 IGF1 受体 (IGF1R) 介导,IGF1R 是一种细胞表面、含有酪氨酸激酶的异四聚体,与许多细胞质信号级联反应相关联。IGF1R 具有强大的抗凋亡、促进生存的能力,在恶性转化中发挥着关键作用。研究已经将 IGF1R 确定为癌症治疗的候选治疗靶点。

我们概述了为治疗目的靶向 IGF 轴的正在进行的努力。我们的综述包括对早期实验工作的总结,这些工作导致 IGF1R 被确定为肿瘤学中的候选治疗靶点。

尽管针对 IGF 轴的靶向治疗在 III 期临床试验中收效甚微,但从这些试验中吸取教训,以合理的方式改进未来的试验非常重要。单独或与化疗或其他生物制剂联合使用抗 IGF1R 抗体和小分子抑制剂的潜力应在随机研究中进一步研究。此外,实施预测性生物标志物来选择患者将改善未来试验的结果。新兴的个性化医疗可能对 IGF1R 靶向治疗产生重大影响。

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