Departament of Developmental Genetics, Instituto de Biotecnología, Universidad Nacional Autónoma de México, Mexico, Mexico.
Cancer Cell Int. 2014 Feb 28;14(1):18. doi: 10.1186/1475-2867-14-18.
General transcription is required for the growth and survival of all living cells. However, tumor cells require extraordinary levels of transcription, including the transcription of ribosomal RNA genes by RNA polymerase I (RNPI) and mRNA by RNA polymerase II (RNPII). In fact, cancer cells have mutations that directly enhance transcription and are frequently required for cancer transformation. For example, the recent discovery that MYC enhances the transcription of the majority genes in the genome correlates with the fact that several transcription interfering drugs preferentially kill cancer cells. In recent years, advances in the mechanistic studies of the basal transcription machinery and the discovery of drugs that interfere with multiple components of transcription are being used to combat cancer. For example, drugs such as triptolide that targets the general transcription factors TFIIH and JQ1 to inhibit BRD4 are administered to target the high proliferative rate of cancer cells. Given the importance of finding new strategies to preferentially sensitize tumor cells, this review primarily focuses on several transcription inhibitory drugs to demonstrate that the basal transcription machinery constitutes a potential target for the design of novel cancer drugs. We highlight the drugs' mechanisms for interfering with tumor cell survival, their importance in cancer treatment and the challenges of clinical application.
一般转录是所有活细胞生长和存活所必需的。然而,肿瘤细胞需要极高水平的转录,包括 RNA 聚合酶 I(RNPI)转录核糖体 RNA 基因和 RNA 聚合酶 II(RNPII)转录 mRNA。事实上,癌细胞有直接增强转录的突变,并且经常是癌症转化所必需的。例如,最近发现 MYC 增强了基因组中大多数基因的转录,这与以下事实相关:几种转录干扰药物优先杀死癌细胞。近年来,对基础转录机制的机制研究的进展以及发现干扰转录多个成分的药物被用于对抗癌症。例如,三萜内酯等靶向一般转录因子 TFIIH 和 JQ1 以抑制 BRD4 的药物被用于靶向癌细胞的高增殖率。鉴于寻找新策略以优先敏化肿瘤细胞的重要性,本综述主要关注几种转录抑制药物,以证明基础转录机制是设计新型癌症药物的潜在靶点。我们强调了这些药物干扰肿瘤细胞存活的机制、它们在癌症治疗中的重要性以及临床应用的挑战。