Døssing Kristina B V, Binderup Tina, Kaczkowski Bogumil, Jacobsen Anders, Rossing Maria, Winther Ole, Federspiel Birgitte, Knigge Ulrich, Kjær Andreas, Friis-Hansen Lennart
Center for Genomic Medicine, Rigshospitalet, Blegdamsvej 9, 2100 Copenhagen, Denmark.
Department of Clinical Physiology, Nuclear Medicine and PET, Rigshospitalet, Blegdamsvej 9, 2100 Copenhagen, Denmark.
Genes (Basel). 2014 Dec 24;6(1):1-21. doi: 10.3390/genes6010001.
Expression of miRNAs in Neuroendocrine Neoplasms (NEN) is poorly characterized. We therefore wanted to examine the miRNA expression in Neuroendocrine Tumors (NETs), and identify their targets and importance in NET carcinogenesis. miRNA expression in six NEN primary tumors, six NEN metastases and four normal intestinal tissues was characterized using miRNA arrays, and validated by in-situ hybridization and qPCR. Among the down-regulated miRNAs miR-129-5p and the let-7f/let-7 family, were selected for further characterization. Transfection of miR-129-5p inhibited growth of a pulmonary and an intestinal carcinoid cell line. Analysis of mRNA expression changes identified EGR1 and G3BP1 as miR-129-5p targets. They were validated by luciferase assay and western blotting, and found robustly expressed in NETs by immunohistochemistry. Knockdown of EGR1 and G3BP1 mimicked the growth inhibition induced by miR-129-5p. let-7 overexpression inhibited growth of carcinoid cell lines, and let-7 inhibition increased protein content of the transcription factor BACH1 and its targets MMP1 and HMGA2, all known to promote bone metastases. Immunohistochemistry analysis revealed that let-7 targets are highly expressed in NETs and metastases. We found down-regulation of miR-129-5p and the let-7 family, and identified new neuroendocrine specific targets for these miRNAs, which contributes to the growth and metastatic potential of these tumors.
微小RNA(miRNA)在神经内分泌肿瘤(NEN)中的表达特征尚不明确。因此,我们希望研究神经内分泌肿瘤(NET)中的miRNA表达情况,并确定其靶点以及在NET致癌过程中的重要性。使用miRNA芯片对6例NEN原发性肿瘤、6例NEN转移灶和4例正常肠组织中的miRNA表达进行了特征分析,并通过原位杂交和定量聚合酶链反应(qPCR)进行了验证。在下调的miRNA中,选择了miR-129-5p和let-7f/let-7家族进行进一步研究。转染miR-129-5p可抑制肺和肠道类癌细胞系的生长。对mRNA表达变化的分析确定早期生长反应蛋白1(EGR1)和G3BP1为miR-129-5p的靶点。通过荧光素酶报告基因检测和蛋白质免疫印迹法对其进行了验证,并通过免疫组织化学法发现它们在NET中大量表达。敲低EGR1和G3BP1可模拟miR-129-5p诱导的生长抑制。过表达let-7可抑制类癌细胞系的生长,抑制let-7可增加转录因子BACH1及其已知可促进骨转移的靶点基质金属蛋白酶1(MMP1)和高迁移率族蛋白A2(HMGA2)的蛋白质含量。免疫组织化学分析显示,let-7的靶点在NET和转移灶中高表达。我们发现miR-129-5p和let-7家族表达下调,并确定了这些miRNA新的神经内分泌特异性靶点,这些靶点有助于这些肿瘤的生长和转移潜能。