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肾细胞癌中的激酶靶点:重新评估旧靶点和发现新靶点。

Kinase targets in renal-cell carcinomas: reassessing the old and discovering the new.

机构信息

Laboratory of Computational Biology, Van Andel Research Institute, Grand Rapids, MI, USA.

出版信息

Lancet Oncol. 2010 Jun;11(6):571-8. doi: 10.1016/S1470-2045(09)70380-8. Epub 2010 Apr 8.

Abstract

Renal-cell carcinoma is a heterogeneous group of tumours that arise in the adult kidneys. Irrespective of the type of renal tumour, traditional chemotherapeutic and radiation-based therapies have been largely ineffective at treating advanced tumours, with long-term survival being very low. Molecularly-targeted inhibitors of protein kinases are effective in delaying progression of advanced renal tumours. These therapies revolve around inhibition of the vascular endothelial growth factor receptor tyrosine kinase and the mammalian target of rapamycin serine or threonine kinase signalling pathways. The genetic complexity of renal tumours revealed by gene-expression profiling and other molecular-genetic technologies indicate that inhibition of additional kinase-associated pathways could also prevent renal tumour growth. In this review, we discuss the use of molecularly-targeted kinase inhibitors in the treatment of renal-cell carcinoma and identify the next generation of kinase inhibitors that show promise for treatment.

摘要

肾细胞癌是一组起源于成人肾脏的异质性肿瘤。无论哪种类型的肾肿瘤,传统的化疗和放疗在治疗晚期肿瘤方面效果甚微,长期生存率非常低。蛋白激酶的分子靶向抑制剂在延缓晚期肾肿瘤的进展方面非常有效。这些疗法主要围绕血管内皮生长因子受体酪氨酸激酶和哺乳动物雷帕霉素靶蛋白丝氨酸/苏氨酸激酶信号通路的抑制展开。基因表达谱和其他分子遗传学技术揭示的肾肿瘤的遗传复杂性表明,抑制其他与激酶相关的通路也可能阻止肾肿瘤的生长。在这篇综述中,我们讨论了分子靶向激酶抑制剂在肾细胞癌治疗中的应用,并确定了下一代有治疗前景的激酶抑制剂。

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