Martínez-Montiel Nancy, Rosas-Murrieta Nora Hilda, Martínez-Montiel Mónica, Gaspariano-Cholula Mayra Patricia, Martínez-Contreras Rebeca D
Laboratorio de Ecología Molecular Microbiana, Centro de Investigaciones en Ciencias Microbiológicas, Instituto de Ciencias, Benemérita Universidad Autónoma de Puebla, Edificio IC11, Ciudad Universitaria, 72570 Colonia San Manuel, PUE, Mexico.
Laboratorio de Bioquímica y Biología Molecular, Instituto de Ciencias, Benemérita Universidad Autónoma de Puebla, Edificio 103H, Ciudad Universitaria, 72550 Colonia San Manuel, PUE, Mexico; Posgrado en Ciencias Químicas, Benemérita Universidad Autónoma de Puebla, Edificio 105 I, Ciudad Universitaria, 72570 Colonia San Manuel, PUE, Mexico.
Biomed Res Int. 2016;2016:3681094. doi: 10.1155/2016/3681094. Epub 2016 Aug 16.
In eukaryotes, genes are frequently interrupted with noncoding sequences named introns. Alternative splicing is a nuclear mechanism by which these introns are removed and flanking coding regions named exons are joined together to generate a message that will be translated in the cytoplasm. This mechanism is catalyzed by a complex machinery known as the spliceosome, which is conformed by more than 300 proteins and ribonucleoproteins that activate and regulate the precision of gene expression when assembled. It has been proposed that several genetic diseases are related to defects in the splicing process, including cancer. For this reason, natural products that show the ability to regulate splicing have attracted enormous attention due to its potential use for cancer treatment. Some microbial metabolites have shown the ability to inhibit gene splicing and the molecular mechanism responsible for this inhibition is being studied for future applications. Here, we summarize the main types of natural products that have been characterized as splicing inhibitors, the recent advances regarding molecular and cellular effects related to these molecules, and the applications reported so far in cancer therapeutics.
在真核生物中,基因常常被名为内含子的非编码序列打断。可变剪接是一种细胞核机制,通过该机制这些内含子被去除,相邻的名为外显子的编码区域连接在一起,生成一条将在细胞质中进行翻译的信息。这种机制由一种称为剪接体的复杂机制催化,剪接体由300多种蛋白质和核糖核蛋白组成,这些蛋白质和核糖核蛋白在组装时激活并调节基因表达的精确性。有人提出,包括癌症在内的几种遗传疾病与剪接过程中的缺陷有关。因此,具有调节剪接能力的天然产物因其在癌症治疗中的潜在用途而备受关注。一些微生物代谢产物已显示出抑制基因剪接的能力,目前正在研究导致这种抑制作用的分子机制,以便用于未来的应用。在此,我们总结了已被鉴定为剪接抑制剂的主要天然产物类型、与这些分子相关的分子和细胞效应的最新进展,以及迄今为止在癌症治疗中的应用报道。