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BET抑制剂在三阴性乳腺癌中的作用

Role of BET Inhibitors in Triple Negative Breast Cancers.

作者信息

Khandekar Durga, Tiriveedhi Venkataswarup

机构信息

Department of Biological Sciences, Tennessee State University, 3500 John A Merritt Blvd, Nashville, TN 37209, USA.

Department of Pharmacology, Vanderbilt University, Nashville, TN 37212, USA.

出版信息

Cancers (Basel). 2020 Mar 25;12(4):784. doi: 10.3390/cancers12040784.

Abstract

Bromodomain and extraterminal domain (BET) proteins have evolved as key multifunctional super-regulators that control gene expression. These proteins have been shown to upregulate transcriptional machinery leading to over expression of genes involved in cell proliferation and carcinogenesis. Based on favorable preclinical evidence of BET inhibitors in various cancer models; currently, 26 clinical trials are underway in various stages of study on various hematological and solid organ cancers. Unfortunately, preliminary evidence for these clinical studies does not support the application of BET inhibitors as monotherapy in cancer treatment. Furthermore, the combinatorial efficiency of BET inhibitors with other chemo-and immunotherapeutic agents remain elusive. In this review, we will provide a concise summary of the molecular basis and preliminary clinical outcomes of BET inhibitors in cancer therapy, with special focus on triple negative breast cancer.

摘要

溴结构域和额外末端结构域(BET)蛋白已演变为控制基因表达的关键多功能超级调节因子。这些蛋白已被证明可上调转录机制,导致参与细胞增殖和致癌作用的基因过度表达。基于BET抑制剂在各种癌症模型中的良好临床前证据;目前,有26项临床试验正在针对各种血液系统和实体器官癌症进行不同阶段的研究。不幸的是,这些临床研究的初步证据不支持将BET抑制剂作为癌症治疗的单一疗法应用。此外,BET抑制剂与其他化学疗法和免疫治疗药物的联合疗效仍不明确。在本综述中,我们将简要总结BET抑制剂在癌症治疗中的分子基础和初步临床结果,特别关注三阴性乳腺癌。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bef7/7226117/7a544ea31187/cancers-12-00784-g001.jpg

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