首页> 美国卫生研究院文献>Frontiers in Genetics >Consensus-Expressed CXCL8 and MMP9 Identified by Meta-Analyzed Perineural Invasion Gene Signature in Gastric Cancer Microarray Data
【2h】

Consensus-Expressed CXCL8 and MMP9 Identified by Meta-Analyzed Perineural Invasion Gene Signature in Gastric Cancer Microarray Data

机译:荟萃表达的CXCL8和MMP9由胃癌微阵列数据中的荟萃分析的神经内侵基因签名鉴定。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

As an underrecognized route of cancer metastasis, perineural invasion (PNI) is defined as the neoplastic invasion of nerves, which can be targeted to inhibit the metastasis of malignant cancer. However, the mechanism underlying PNI in cancer is largely unknown. We constructed a PNI gene signature based on a Pathway Studio–mediated literature screen and investigated the relevant genes in a gastric cancer model. Thus, a total of 467 studies/datasets were retrieved from the Gene Expression Omnibus database using the keyword “gastric cancer,” among which 13 studies that focused on gene expression profiling were further manually inspected and selected. Furthermore, the constructed PNI gene signature (104 genes) expression was meta-analyzed, and the consensus-expressed C-X-C motif chemokine ligand 8 (CXCL8) and matrix metallopeptidase 9 (MMP9) (p < 0.01, |log fold change| >1) were detected. Importantly, the disease-free survival was significantly worse in patients with high expressions of CXCL8 and MMP9 than in those with low expressions (p = 0.05). Moreover, multiple linear regression analysis showed that the population region (country) was associated with the expressions of both CXCL8 and MMP9. In conclusion, these data suggest that the coexpression of CXCL8 and MMP9 could be an early detection marker for PNI, with a potential to be utilized as individual therapy targets for early treatment to prevent PNI-related cancer metastasis.
机译:作为一种尚未被广泛认识的癌症转移途径,神经周围侵犯(PNI)被定义为神经的肿瘤浸润,其靶向作用可能是抑制恶性肿瘤的转移。但是,在癌症中潜在的PNI机制尚不清楚。我们基于Pathway Studio介导的文献筛选构建了PNI基因签名,并研究了胃癌模型中的相关基因。因此,使用关键词“胃癌”从“基因表达综合”数据库中检索了总共467个研究/数据集,其中还有13个专注于基因表达谱分析的研究被进一步手动检查和选择。此外,对构建的PNI基因签名(104个基因)表达进行了荟萃分析,并以共识表达的CXC基序趋化因子配体8(CXCL8)和基质金属肽酶9(MMP9)(p <0.01,|对数倍变化|> 1)。被检测到。重要的是,高表达CXCL8和MMP9的患者的无病生存期显着低于低表达的患者(p = 0.05)。此外,多元线性回归分析表明,人口区域(国家)与CXCL8和MMP9的表达均相关。总之,这些数据表明,CXCL8和MMP9的共表达可能是PNI的早期检测标志物,有可能被用作早期治疗的个体治疗靶点,以预防PNI相关的癌症转移。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号