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Differences between CAFs and their paired NCF from adjacent colonic mucosa reveal functional heterogeneity of CAFs providing prognostic information

机译:CAF及其配对的NCF与邻近结肠粘膜之间的差异揭示了CAF的功能异质性提供了预后信息

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摘要

Little is known about the difference in gene expression between carcinoma‐associated fibroblasts (CAFs) and paired normal colonic fibroblasts (NCFs) in colorectal cancer. Paired CAFs and NCFs were isolated from eight primary human colorectal carcinoma specimens. In culture conditions, soluble factors secreted by CAFs in the conditioned media increased clonogenicity and migration of epithelial cancer cells lines to a greater extent than did NCF. In vivo, CAFs were more competent as tumour growth enhancers than paired NCFs when co‐inoculated with colorectal cell lines. Gene expression analysis of microarrays of CAF and paired NCF populations enabled us to identify 108 deregulated genes (38 upregulated and 70 downregulated genes). Most of those genes are fibroblast‐specific. This has been validated in silico in dataset and by qPCR in selected genes. GSEA analysis revealed a differential transcriptomic profile of CAFs, mainly involving the Wnt signallingsignalling pathway, focal adhesion and cell cycle. Both deregulated genes and biological processes involved depicted a considerable degree of overlap with deregulated genes reported in breast, lung, oesophagus and prostate CAFs. These observations suggest that similar transcriptomic programs may be active in the transition from normal fibroblast in adjacent tissues to CAFs, independently of their anatomic demarcation. Additionally NCF already depicted an activated pattern associated with inflammation.The deregulated genes signature score seemed to correlate with CAF tumour promoter abilities in vitro, suggesting a high degree of heterogeneity between CAFs, and it has also prognostic value in two independent datasets.Further characterization of the roles these biomarkers play in cancer will reveal how CAFs provide cancer cells with a suitable microenvironment and may help in the development of new therapeutic targets for cancer treatment.
机译:对于结直肠癌中癌相关的成纤维细胞(CAF)和成对的正常结肠成纤维细胞(NCF)之间的基因表达差异知之甚少。配对的CAF和NCFs从八个原发性人类大肠癌标本中分离出来。在培养条件下,条件培养液中CAF分泌的可溶性因子比NCF更大程度地提高了上皮癌细胞系的克隆形成性和迁移。在体内,当与结直肠细胞系共同接种时,CAF比配对的NCF更能充当肿瘤生长促进剂。 CAF和配对的NCF群体的微阵列的基因表达分析使我们能够鉴定108个失调基因(38个上调基因和70个下调基因)。这些基因大多数是成纤维细胞特异性的。这已经在数据集中通过计算机验证,并通过qPCR在选定的基因中得到验证。 GSEA分析揭示了CAFs的差异转录组谱,主要涉及Wnt信号转导途径,粘着斑和细胞周期。失调的基因和所涉及的生物学过程都与乳腺癌,肺,食道和前列腺CAFs中报道的失调的基因有相当程度的重叠。这些观察结果表明,类似的转录组程序可能在从邻近组织中的正常成纤维细胞向CAF的过渡中起作用,而与它们的解剖学界限无关。此外,NCF已经描绘出一种与炎症相关的激活模式。失调的基因签名评分似乎与CAF肿瘤启动子的体外能力相关,表明CAF之间存在高度异质性,并且在两个独立的数据集中也具有预后价值。这些生物标记物在癌症中的作用将揭示CAF如何为癌细胞提供合适的微环境,并可能有助于开发新的癌症治疗靶标。

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