Upstream open reading frames: new players in the landscape of cancer gene regulation.

IF 3.4 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY NAR cancer Pub Date : 2024-05-20 eCollection Date: 2024-06-01 DOI:10.1093/narcan/zcae023
Anwesha Dasgupta, John R Prensner
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Abstract

The translation of RNA by ribosomes represents a central biological process and one of the most dysregulated processes in cancer. While translation is traditionally thought to occur exclusively in the protein-coding regions of messenger RNAs (mRNAs), recent transcriptome-wide approaches have shown abundant ribosome activity across diverse stretches of RNA transcripts. The most common type of this kind of ribosome activity occurs in gene leader sequences, also known as 5' untranslated regions (UTRs) of the mRNA, that precede the main coding sequence. Translation of these upstream open reading frames (uORFs) is now known to occur in upwards of 25% of all protein-coding genes. With diverse functions from RNA regulation to microprotein generation, uORFs are rapidly igniting a new arena of cancer biology, where they are linked to cancer genetics, cancer signaling, and tumor-immune interactions. This review focuses on the contributions of uORFs and their associated 5'UTR sequences to cancer biology.

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上游开放阅读框:癌症基因调控格局中的新角色。
核糖体翻译 RNA 是一个核心的生物过程,也是癌症中最失调的过程之一。虽然传统上认为翻译只发生在信使核糖核酸(mRNA)的蛋白质编码区,但最近的全转录组方法显示,核糖体在不同的 RNA 转录本中具有丰富的活性。这种核糖体活动最常见的类型出现在基因领导序列,也称为 mRNA 的 5' 非翻译区 (UTR),即主编码序列之前。目前已知这些上游开放阅读框(uORF)的翻译发生在所有蛋白质编码基因中的 25% 以上。uORFs具有从RNA调控到微蛋白生成的多种功能,正在迅速点燃癌症生物学的新领域,它们与癌症遗传学、癌症信号转导和肿瘤-免疫相互作用息息相关。本综述将重点探讨 uORFs 及其相关 5'UTR 序列对癌症生物学的贡献。
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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来源期刊
CiteScore
6.90
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0.00%
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审稿时长
13 weeks
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Correction to 'Ku-DNA binding inhibitors modulate the DNA damage response in response to DNA double-strand breaks'. CytoCellDB: a comprehensive resource for exploring extrachromosomal DNA in cancer cell lines. DNA abasic sites act as rational therapeutic targets to synergize temozolomide response in both MMR-proficient and deficient cancer. High-level tumour methylation of BRCA1 and RAD51C is required for homologous recombination deficiency in solid cancers. Decoding ribosome complexity: role of ribosomal proteins in cancer and disease.
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