Venables Julian P
University of Newcastle-upon-Tyne, Institute of Human Genetics, International Centre for Life, Central Parkway, Newcastle-upon-Tyne, United Kingdom.
Cancer Res. 2004 Nov 1;64(21):7647-54. doi: 10.1158/0008-5472.CAN-04-1910.
Pre-mRNA splicing is a sophisticated and ubiquitous nuclear process, which is a natural source of cancer-causing errors in gene expression. Intronic splice site mutations of tumor suppressor genes often cause exon-skipping events that truncate proteins just like classical nonsense mutations. Also, many studies over the last 20 years have reported cancer-specific alternative splicing in the absence of genomic mutations. Affected proteins include transcription factors, cell signal transducers, and components of the extracellular matrix. Antibodies against alternatively spliced products on cancer cells are currently in clinical trials, and competitive reverse transcription-PCR across regions of alternative splicing is being used as a simple diagnostic test. As well as being associated with cancer, the nature of the alternative gene products is usually consistent with an active role in cancer; therefore, the alternative splicing process itself is a potential target for gene therapy.
前体信使核糖核酸(pre-mRNA)剪接是一种复杂且普遍存在的细胞核过程,它是基因表达中致癌错误的天然来源。肿瘤抑制基因的内含子剪接位点突变常常导致外显子跳跃事件,这会像经典的无义突变一样使蛋白质截短。此外,在过去20年里,许多研究报道了在不存在基因组突变的情况下出现的癌症特异性可变剪接。受影响的蛋白质包括转录因子、细胞信号转导器以及细胞外基质的成分。针对癌细胞上可变剪接产物的抗体目前正在进行临床试验,并且跨可变剪接区域的竞争性逆转录聚合酶链反应(PCR)正被用作一种简单的诊断测试。除了与癌症相关外,可变基因产物的性质通常与在癌症中发挥的积极作用一致;因此,可变剪接过程本身是基因治疗的一个潜在靶点。