Department of Biochemistry, University of Lausanne, Epalinges, Switzerland.
EMBO J. 2013 Aug 14;32(16):2248-63. doi: 10.1038/emboj.2013.156. Epub 2013 Jul 16.
Squamous cell carcinomas (SCCs) are highly heterogeneous tumours, resulting from deranged expression of genes involved in squamous cell differentiation. Here we report that microRNA-34a (miR-34a) functions as a novel node in the squamous cell differentiation network, with SIRT6 as a critical target. miR-34a expression increases with keratinocyte differentiation, while it is suppressed in skin and oral SCCs, SCC cell lines, and aberrantly differentiating primary human keratinocytes (HKCs). Expression of this miRNA is restored in SCC cells, in parallel with differentiation, by reversion of genomic DNA methylation or wild-type p53 expression. In normal HKCs, the pro-differentiation effects of increased p53 activity or UVB exposure are miR-34a-dependent, and increased miR-34a levels are sufficient to induce differentiation of these cells both in vitro and in vivo. SIRT6, a sirtuin family member not previously connected with miR-34a function, is a direct target of this miRNA in HKCs, and SIRT6 down-modulation is sufficient to reproduce the miR-34a pro-differentiation effects. The findings are of likely biological significance, as SIRT6 is oppositely expressed to miR-34a in normal keratinocytes and keratinocyte-derived tumours.
鳞状细胞癌(SCCs)是高度异质性的肿瘤,源于参与鳞状细胞分化的基因表达失调。在这里,我们报告 miR-34a(miR-34a)作为鳞状细胞分化网络中的一个新节点,SIRT6 是一个关键靶点。miR-34a 的表达随着角质形成细胞的分化而增加,而在皮肤和口腔 SCCs、SCC 细胞系和异常分化的原代人角质形成细胞(HKCs)中则受到抑制。通过逆转基因组 DNA 甲基化或野生型 p53 表达,可在 SCC 细胞中恢复该 miRNA 的表达,同时伴随分化。在正常的 HKCs 中,增加的 p53 活性或 UVB 暴露的促分化作用依赖于 miR-34a,并且增加的 miR-34a 水平足以诱导这些细胞在体外和体内分化。SIRT6 是先前与 miR-34a 功能无关的 Sirtuin 家族成员,是该 miRNA 在 HKCs 中的直接靶标,下调 SIRT6 足以再现 miR-34a 的促分化作用。这些发现具有重要的生物学意义,因为 SIRT6 在正常角质形成细胞和角质形成细胞来源的肿瘤中与 miR-34a 的表达相反。