用蛋白药物靶向MYC。

3区 生物学 Q2 Biochemistry, Genetics and Molecular Biology
Jumi A Shin
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引用次数: 0

摘要

继心血管疾病之后,癌症是我们最大的杀手。1971年,“向癌症宣战”正式启动;尽管经过了几十年的研究和发展,我们的抗癌药物仍然主要由小分子组成。然而,蛋白质药物有望成为针对MYC的下一代药物的基础,MYC是一种编码MYC转录因子的原癌基因,与大多数人类癌症有关。这些蛋白质药物在细胞核内的细胞内起作用,在那里它们直接与基因组相互作用,或者可以与MYC合作以减弱其有害活动。目前还没有小分子药物能够成功对抗MYC,但是蛋白质药物Omomyc已经在人体试验中成功地抑制了实体瘤。尽管MYC是正常细胞过程的关键调节因子,但当MYC失控时,我们需要开发新的策略来遏制它。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Targeting MYC with protein drugs.

After cardiovascular disease, cancer is our biggest killer. The "war on cancer" officially launched in 1971; despite decades of research and development, our arsenal of drugs against cancer still comprises mainly small molecules. Protein drugs, however, are poised to become the foundation for next-generation drugs that target MYC, a proto-oncogene that encodes the MYC transcription factor involved in the majority of human cancers. Such protein drugs work inside the cell in the nucleus, where they interact directly with the genome or can partner with MYC to blunt its detrimental activities. No small-molecule drug has been successful against MYC, but protein drug Omomyc has successfully inhibited solid tumors in human trials. Although MYC is a key regulator of normal cellular processes, we need to develop new tactics to contain MYC when it goes rogue.

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来源期刊
CiteScore
6.90
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: Progress in Molecular Biology and Translational Science (PMBTS) provides in-depth reviews on topics of exceptional scientific importance. If today you read an Article or Letter in Nature or a Research Article or Report in Science reporting findings of exceptional importance, you likely will find comprehensive coverage of that research area in a future PMBTS volume.
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