a Istituto per l'Endocrinologia e l'Oncologia Sperimentale (IEOS) "G. Salvatore", Consiglio Nazionale delle Ricerche (CNR), c/o Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università degli Studi di Napoli "Federico II" , Naples , Italy.
b Instituto Nacional de Câncer - INCA, Centro de Pesquisas (CPQ) , Rio de Janeiro , RJ , Brazil.
Cell Cycle. 2017;16(23):2282-2289. doi: 10.1080/15384101.2017.1380127. Epub 2017 Nov 9.
DICER1 plays a central role in the biogenesis of microRNAs and it is important for normal development. Altered microRNA expression and DICER1 dysregulation have been described in several types of tumors, including thyroid carcinomas. Recently, our group identified a new somatic mutation (c.5438A>G; E1813G) within DICER1 gene of an unknown function. Herein, we show that DICER1 is overexpressed, at mRNA level, in a significant-relative number of papillary (70%) and anaplastic (42%) thyroid carcinoma samples, whereas is drastically downregulated in all the analyzed human thyroid carcinoma cell lines (TPC-1, BCPAP, FRO and 8505c) in comparison with normal thyroid tissue samples. Conversely, DICER1 is downregulated, at protein level, in PTC in comparison with normal thyroid tissues. Our data also reveals that DICER1 overexpression positively regulates thyroid cell proliferation, whereas its silencing impairs thyroid cell differentiation. The expression of DICER1 gene mutation (c.5438A>G; E1813G) negatively affects the microRNA machinery and cell proliferation as well as upregulates DICER1 protein levels of thyroid cells but has no impact on thyroid differentiation. In conclusion, DICER1 protein is downregulated in papillary thyroid carcinomas and affects thyroid proliferation and differentiation, while DICER1 gene mutation (c.5438A>G; E1813G) compromises the DICER1 wild-type-mediated microRNA processing and cell proliferation.
DICER1 在 microRNA 的生物发生中发挥核心作用,对正常发育很重要。几种类型的肿瘤,包括甲状腺癌,已经描述了 microRNA 表达的改变和 DICER1 失调。最近,我们小组在 DICER1 基因中发现了一个新的体细胞突变(c.5438A>G;E1813G),其功能未知。在此,我们表明 DICER1 在大量的甲状腺乳头状癌(70%)和间变性甲状腺癌(42%)样本中,在 mRNA 水平上过度表达,而在所有分析的人类甲状腺癌细胞系(TPC-1、BCPAP、FRO 和 8505c)中与正常甲状腺组织样本相比,其表达水平则明显下调。相反,与正常甲状腺组织相比,DICER1 在 PTC 中蛋白水平下调。我们的数据还表明,DICER1 过表达可正向调节甲状腺细胞增殖,而其沉默则损害甲状腺细胞分化。DICER1 基因突变(c.5438A>G;E1813G)的表达既影响微 RNA 机制和细胞增殖,又上调甲状腺细胞中 DICER1 蛋白水平,但对甲状腺分化没有影响。总之,DICER1 蛋白在甲状腺乳头状癌中下调,并影响甲状腺的增殖和分化,而 DICER1 基因突变(c.5438A>G;E1813G)则损害 DICER1 野生型介导的 microRNA 加工和细胞增殖。