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成骨肉瘤细胞系的功能特征分析及与侵袭性癌症表型相关的 mRNA 和 miRNA 的鉴定。

Functional characterisation of osteosarcoma cell lines and identification of mRNAs and miRNAs associated with aggressive cancer phenotypes.

机构信息

1] Cancer Stem Cell Innovation Centre, Institute of Cancer Research, Oslo University Hospital, The Norwegian Radium Hospital, PO Box 4953, Nydalen, Oslo 0424, Norway [2] Department of Tumor Biology, Institute of Cancer Research, Oslo University Hospital, The Norwegian Radium Hospital, PO Box 4953, Nydalen, Oslo 0424, Norway.

出版信息

Br J Cancer. 2013 Oct 15;109(8):2228-36. doi: 10.1038/bjc.2013.549. Epub 2013 Sep 24.

Abstract

BACKGROUND

Osteosarcoma is the most common primary malignant bone tumour, predominantly affecting children and adolescents. Cancer cell line models are required to understand the underlying mechanisms of tumour progression and for preclinical investigations.

METHODS

To identify cell lines that are well suited for studies of critical cancer-related phenotypes, such as tumour initiation, growth and metastasis, we have evaluated 22 osteosarcoma cell lines for in vivo tumorigenicity, in vitro colony-forming ability, invasive/migratory potential and proliferation capacity. Importantly, we have also identified mRNA and microRNA (miRNA) gene expression patterns associated with these phenotypes by expression profiling.

RESULTS

The cell lines exhibited a wide range of cancer-related phenotypes, from rather indolent to very aggressive. Several mRNAs were differentially expressed in highly aggressive osteosarcoma cell lines compared with non-aggressive cell lines, including RUNX2, several S100 genes, collagen genes and genes encoding proteins involved in growth factor binding, cell adhesion and extracellular matrix remodelling. Most notably, four genes-COL1A2, KYNU, ACTG2 and NPPB-were differentially expressed in high and non-aggressive cell lines for all the cancer-related phenotypes investigated, suggesting that they might have important roles in the process of osteosarcoma tumorigenesis. At the miRNA level, miR-199b-5p and mir-100-3p were downregulated in the highly aggressive cell lines, whereas miR-155-5p, miR-135b-5p and miR-146a-5p were upregulated. miR-135b-5p and miR-146a-5p were further predicted to be linked to the metastatic capacity of the disease.

INTERPRETATION

The detailed characterisation of cell line phenotypes will support the selection of models to use for specific preclinical investigations. The differentially expressed mRNAs and miRNAs identified in this study may represent good candidates for future therapeutic targets. To our knowledge, this is the first time that expression profiles are associated with functional characteristics of osteosarcoma cell lines.

摘要

背景

骨肉瘤是最常见的原发性恶性骨肿瘤,主要影响儿童和青少年。为了了解肿瘤进展的潜在机制并进行临床前研究,需要使用癌细胞系模型。

方法

为了鉴定适合研究关键癌症相关表型(如肿瘤起始、生长和转移)的细胞系,我们评估了 22 种骨肉瘤细胞系的体内致瘤性、体外集落形成能力、侵袭/迁移潜力和增殖能力。重要的是,我们还通过表达谱鉴定了与这些表型相关的 mRNA 和 microRNA(miRNA)基因表达模式。

结果

这些细胞系表现出广泛的癌症相关表型,从相当惰性到非常侵袭性。与非侵袭性细胞系相比,高度侵袭性骨肉瘤细胞系中多个 mRNA 表达水平存在差异,包括 RUNX2、几个 S100 基因、胶原基因以及参与生长因子结合、细胞黏附和细胞外基质重塑的蛋白编码基因。最值得注意的是,在所有研究的癌症相关表型中,COL1A2、KYNU、ACTG2 和 NPPB 这四个基因在高侵袭性和非侵袭性细胞系中均有差异表达,这表明它们可能在骨肉瘤肿瘤发生过程中具有重要作用。在 miRNA 水平,miR-199b-5p 和 miR-100-3p 在高度侵袭性细胞系中下调,而 miR-155-5p、miR-135b-5p 和 miR-146a-5p 上调。miR-135b-5p 和 miR-146a-5p 进一步被预测与疾病的转移能力有关。

结论

细胞系表型的详细特征将支持选择用于特定临床前研究的模型。本研究中鉴定的差异表达的 mRNA 和 miRNA 可能代表未来治疗靶点的良好候选物。据我们所知,这是首次将表达谱与骨肉瘤细胞系的功能特征相关联。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd1c/3798956/4ec77ee907a0/bjc2013549f1.jpg

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