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Matrigel Basement Membrane Matrix influences expression of microRNAs in cancer cell lines

机译:Matrigel基质膜基质影响癌细胞系中微小RNA的表达

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摘要

Matrigel is a medium rich in extracellular matrix (ECM) components used for three-dimensional cell culture and is known to alter cellular phenotypes and gene expression. microRNAs (miRNAs) are small, non-coding RNAs that regulate gene expression and have roles in cancer. While miRNA profiles of numerous cell lines cultured on plastic have been reported, the influence of Matrigel-based culture on cancer cell miRNA expression is largely unknown. This study investigated the influence of Matrigel on the expression of miRNAs that might facilitate ECM-associated cancer cell growth. We performed miRNA profiling by microarray using two colon cancer cell lines (SW480 and SW620), identifying significant differential expression of miRNAs between cells cultured in Matrigel and on plastic. Many of these miRNAs have previously been implicated in cancer-related processes. A common Matrigel-induced miRNA signature comprised of up-regulated miR-1290 and miR-210 and down-regulated miR-29b and miR-32 was identified using RT-qPCR across five epithelial cancer cell lines (SW480, SW620, HT-29, A549 and MDA-MB-231). Experimental modulation of these miRNAs altered expression of their known target mRNAs involved in cell adhesion, proliferation and invasion, in colon cancer cell lines. Furthermore, ITGA5 was identified as a novel putative target of miR-32 that may facilitate cancer cell interactions with the ECM. We propose that culture of cancer cell lines in Matrigel more accurately recapitulates miRNA expression and function in cancer than culture on plastic and thus is a valuable approach to the in vitro study of miRNAs.
机译:Matrigel是一种富含细胞外基质(ECM)组分的中型,用于三维细胞培养,已知改变细胞表型和基因表达。 microRNAs(miRNA)是小的,非编码RNA调节基因表达并在癌症中具有作用。虽然已经报道了诸如塑料培养的许多细胞系的miRNA谱,但基于基于Matrigel的培养物对癌细胞miRNA表达的影响很大程度上是未知的。本研究研究了Matrigel对可能促进ECM相关癌细胞生长的miRNA表达的影响。我们使用两种结肠癌细胞系(SW480和SW620)进行微阵列进行miRNA分析,识别MiRNA在Matrigel和塑料上培养的细胞之间的显着差异表达。其中许多miRNA以前涉及与癌症相关的过程。使用具有UT-QPCR的常见的MIR-1290和MIR-210以及下调MIR-29B和MIR-32组成的常见的Matrigel诱导的miRNA签名,其横跨五种上皮癌细胞系(SW480,SW620,HT-29 ,A549和MDA-MB-231)。这些miRNA的实验调节改变了它们在结肠癌细胞系中涉及细胞粘附,增殖和侵袭的已知靶MRNA的表达。此外,ITGA5被鉴定为MIR-32的新推定靶标,这可能促进癌细胞与ECM相互作用。我们提出了Matrigel中的癌细胞系培养更准确地重新鉴定miRNA表达和癌症的功能而不是塑料的培养,因此是MiRNA的体外研究的有价值的方法。

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  • 作者单位

    Laboratory for Cancer Medicine Western Australian Inst. for Medical Research Univ. of Western;

    Centre for Cancer Biology SA Pathology Adelaide SA 5000 Australia School of Molecular and;

    Laboratory for Cancer Medicine Western Australian Inst. for Medical Research Univ. of Western;

    Centre for Cancer Biology SA Pathology Adelaide SA 5000 Australia;

    Laboratory for Cancer Medicine Western Australian Inst. for Medical Research Univ. of Western;

    Laboratory for Cancer Medicine Angiogenesis Unit Western Australian Inst. for Medical Research;

    Centre for Cancer Biology SA Pathology Adelaide SA 5000 Australia School of Molecular and;

    Laboratory for Cancer Medicine Western Australian Inst. for Medical Research Univ. of Western;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物化学;
  • 关键词

    Cancer; Cell culture; Matrigel; MicroRNA;

    机译:癌症;细胞培养;matrigel;microRNA;

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