Targeting translation initiation in breast cancer

A. Akcakanat, D. Hong, F. Meric-Bernstam
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引用次数: 3

Abstract

Over the past 20 years, a better understanding of cancer biology, screening for early detection, improved adjuvant treatment, and targeted therapies have decreased the rate of breast cancer deaths. However, resistance to treatment is common, and new approaches are needed. Deregulation of translation initiation is associated with the commencement and progression of cancer. Often, translation initiation factors are overexpressed and the related signaling pathways activated in human tumors. Recently, a significant number of inhibitors that target translation factors and pathways have become available. These inhibitors are being tested alone or in combination with chemotherapeutic agents in clinical trials. The results are varied, and it is not yet clear which drug treatments most effectively inhibit tumor growth. This review highlights the pathways and downstream effects of the activation of translation and discusses targeting the control of translation initiation as a therapeutic approach in cancer, focusing on breast cancer clinical trials.
靶向乳腺癌翻译起始
在过去的20年里,对癌症生物学的更好理解、早期发现的筛查、改进的辅助治疗和靶向治疗降低了乳腺癌的死亡率。然而,对治疗的耐药性是常见的,需要新的方法。翻译起始的失调与癌症的发生和发展有关。在人类肿瘤中,翻译起始因子经常过度表达,相关信号通路被激活。最近,大量针对翻译因子和途径的抑制剂已经可用。这些抑制剂正在临床试验中单独或与化疗药物联合进行测试。结果各不相同,目前尚不清楚哪种药物治疗最有效地抑制肿瘤生长。这篇综述强调了翻译激活的途径和下游效应,并讨论了靶向控制翻译起始作为一种治疗癌症的方法,重点是乳腺癌临床试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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