Plateroti Michelina, de Araujo Patricia Rosa, da Silva Acarizia Eduardo, Penalva Luiz O F
Centre de Génétique et de Physiologie Moléculaire et Cellulaire, Université Claude Bernard Lyon 1, France. 16 Rue Raphael Dubois, 69622 Villeurbanne, Cedex France.
Curr Colorectal Cancer Rep. 2012;8(4):290-297. doi: 10.1007/s11888-012-0141-6.
Aberrant gene expression is the cause and the consequence of tumorigenesis. A major component of gene expression is translation regulation; a process whose main players are RNA-binding-proteins (RBPs). More than 800 RBPs have been identified in the human genome and several of them have been shown to control gene networks associated with relevant cancer processes. A more systematic characterization of RBPs starts to reveal that similar to transcription factors, they can function as tumor suppressors or oncogenes. A relevant example is Musashi1 (Msi1), which is emerging as a critical regulator of tumorigenesis in multiple cancer types, including colon cancer. Msi1 is a stem marker in several tissues and is critical in maintaining the balance between self-renewal and differentiation. However, a boost in Msi1 expression can most likely lead cells towards an oncogenic pathway. In this article, we discuss the parallels between Msi1 function in normal renewal of intestinal epithelium and in colon cancer.
异常基因表达既是肿瘤发生的原因,也是其结果。基因表达的一个主要组成部分是翻译调控,这一过程的主要参与者是RNA结合蛋白(RBPs)。人类基因组中已鉴定出800多种RBPs,其中一些已被证明可控制与相关癌症过程相关的基因网络。对RBPs进行更系统的表征开始揭示,与转录因子类似,它们可以作为肿瘤抑制因子或癌基因发挥作用。一个相关的例子是Musashi1(Msi1),它正成为包括结肠癌在内的多种癌症类型中肿瘤发生的关键调节因子。Msi1是几种组织中的干细胞标志物,对维持自我更新和分化之间的平衡至关重要。然而,Msi1表达的增加很可能会使细胞走向致癌途径。在本文中,我们讨论了Msi1在正常肠上皮更新和结肠癌中的功能之间的相似之处。