首页> 美国卫生研究院文献>Aging (Albany NY) >B7-CD28 gene family expression is associated with prognostic and immunological characteristics of diffuse large B-cell lymphoma
【2h】

B7-CD28 gene family expression is associated with prognostic and immunological characteristics of diffuse large B-cell lymphoma

机译:B7-CD28基因家族表达与弥漫性大B细胞淋巴瘤的预后和免疫学特征相关

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

The B7-CD28 gene family plays a key role in regulating cellular immunity and is closely related to tumorigenesis and immune evasion. Here, we explored associations between clinical and immune features and B7-CD28 gene family expression in Gene Expression Omnibus (GEO) datasets representing 1812 diffuse large B-cell lymphoma (DLBCL) patients. This included 414 in the training cohort and 470 and 928 patients in the and validation cohorts, respectively. Four survival-associated genes identified in the cohort by univariate Cox analysis were incorporated into a multivariate analysis, ultimately establishing a three-gene risk signature. Risk scores assigned based on expression of these genes were validated by Kaplan–Meier and multivariable Cox analyses in the remaining datasets and in important clinical subsets. High-risk patients had shorter overall survival and, in some cases, progression-free survival than low-risk patients. Additionally, expression of programmed cell death 1 (PD-1) and programmed death ligand 1 (PD-L1), as well as several other important immune checkpoint genes, differed between high-risk and low-risk patients, as did the proportions of various immune-infiltrating cells. Finally, further analysis confirmed that these B7-CD28 genes play important roles in immune responses altered in DLBCL.
机译:B7-CD28基因家族在调节细胞免疫中起关键作用,并且与肿瘤发生和免疫逃避密切相关。在这里,我们探讨了代表1812弥漫性大B细胞淋巴瘤(DLBCL)患者的基因表达综合(GEO)数据集中B7-CD28基因家族表达与临床和免疫特征之间的关联。这包括训练队列中的414名患者和验证队列中的470名患者和928名患者。通过单变量Cox分析在队列中确定的四个与生存相关的基因被纳入多变量分析,最终建立了三基因风险特征。根据这些基因的表达分配的风险评分已通过Kaplan-Meier和多变量Cox分析在其余数据集中和重要的临床子集中进行了验证。与低风险患者相比,高风险患者的总生存期较短,并且在某些情况下无进展生存期。此外,高危和低危患者的程序性细胞死亡1(PD-1)和程序性死亡配体1(PD-L1)以及其他几个重要的免疫检查点基因的表达也有所不同,各种免疫浸润细胞。最后,进一步的分析证实了这些B7-CD28基因在DLBCL中改变的免疫应答中起重要作用。

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