Jannot G, Simard M J
Laval University Cancer Research Center, Hôtel-Dieu de Québec (CHUQ), Quebec City, Québec, Canada.
Oncogene. 2006 Oct 9;25(46):6197-201. doi: 10.1038/sj.onc.1209921.
Altering cell proliferation and differentiation are usually key events leading to cancer. As originally demonstrated by Sydney Brenner in 1960s, the nematode Caenorhabditis elegans represents an animal model of choice to study mechanisms important to maintain proper cellular behaviour. This round worm has helped to elucidate components as well as new cellular pathways required for animal development. Among them, the discovery of the programmed cell death and non-coding RNAs (microRNAs) controlling gene expression are two remarkable examples. Recently, two studies have demonstrated, once again, that using C. elegans can help gathering insights on cellular mechanisms leading to tumour formation. Two microRNAs, miR-84 and miR-61, control the expression of the oncogene orthologues Ras and Vav indicating their capacity to act as tumour suppressors. These observations demonstrate that uncovering the function of microRNAs is important to increase our understanding of cancer.
改变细胞增殖和分化通常是导致癌症的关键事件。正如悉尼·布伦纳在20世纪60年代最初所证明的那样,线虫秀丽隐杆线虫是研究维持正常细胞行为重要机制的首选动物模型。这种蛔虫有助于阐明动物发育所需的组成部分以及新的细胞途径。其中,程序性细胞死亡的发现和控制基因表达的非编码RNA(微小RNA)就是两个显著的例子。最近,两项研究再次表明,利用秀丽隐杆线虫有助于深入了解导致肿瘤形成的细胞机制。两种微小RNA,miR-84和miR-61,控制癌基因同源物Ras和Vav的表达,表明它们具有作为肿瘤抑制因子的作用。这些观察结果表明,揭示微小RNA的功能对于增进我们对癌症的理解很重要。