首页> 外文期刊>Cellular oncology >Tumor necrosis factor-a is associated with positive lymph node status in patients with recurrence of colorectal cancer - indications for anti-TNF-alpha agents in cancer treatment
【24h】

Tumor necrosis factor-a is associated with positive lymph node status in patients with recurrence of colorectal cancer - indications for anti-TNF-alpha agents in cancer treatment

机译:大肠癌复发患者的肿瘤坏死因子-a与阳性淋巴结状态有关-癌症治疗中抗TNF-α药物的适应症

获取原文
获取原文并翻译 | 示例

摘要

Introduction: The progressive growth of malignancies is accompanied by a decline in the immune response through mechanisms which are poorly understood. Apoptosis and induction of inflammation by tumor released cytokines as tumor escape mechanisms have been proposed to play an important role in colorectal carcinogenesis.Methods: Expression of Tumor necrosis factor-alpha (TNF-a) was analyzed in colorectal cancer specimen and the cancer cell line HT-29 by immunohistochemistry and RT-PCR. TNF-a expression on protein and mRNA level were correlated with clinical characteristics and impact on survival. TNFR-1 was co-labelled with TNF-a and CD8+ cytotoxic T cells in immunofluorescence double staining experiments.Results: 94% (n = 98/104) of the patients with CRC expressed TNF-a. High TNF-a expression was significantly associated with positive lymph node stage and recurrence of the tumor. Multivariate analysis revealed high TNF-a expression as an independent prognostic factor. Immunohistochemistry was correlated with RT-PCR results (r = 0.794). Immunofluorescence double staining experiments revealed increased TNFR-1 expression by CD8+ cells.Conclusions: TNF-a expression by tumor cells may be an efficient immunological escape mechanism by inflammation-enhanced metastases and probably by induction of apoptosis in tumor-infiltrating CD8+ immune cells resulting in a down regulation of the tumoral immune response. Our data support the role of tumor-derived TNF-a expression as an important promoter of tumoral immune escape mechanisms and malignant progression, and suggest that analysis on either protein (immunohistochemistry) or RNA level (RT-PCR) can be used effectively in this respect. Targeting TNF-a may be a promising option, especially in cases with high TNF-a expression and positive lymph node metastases.
机译:简介:恶性肿瘤的逐步发展伴随着免疫应答的下降,其机制尚不清楚。已经提出肿瘤释放细胞因子的凋亡和诱导炎症作为肿瘤逃逸机制在大肠癌发生中起重要作用。方法:分析大肠癌标本和癌细胞系中肿瘤坏死因子-α(TNF-a)的表达HT-29通过免疫组织化学和RT-PCR。 TNF-α在蛋白质和mRNA水平上的表达与临床特征及其对生存的影响有关。在免疫荧光双重染色实验中,TNFR-1与TNF-a和CD8 +细胞毒性T细胞共标记。结果:CRC患者中94%(n = 98/104)表达TNF-a。高TNF-α表达与阳性淋巴结分期和肿瘤复发显着相关。多变量分析显示高TNF-α表达是独立的预后因素。免疫组织化学与RT-PCR结果相关(r = 0.794)。免疫荧光双染色实验显示CD8 +细胞表达的TNFR-1增加。结论:肿瘤细胞TNF-a表达可能是炎症增强转移的一种有效的免疫逃逸机制,可能是通过诱导肿瘤浸润的CD8 +免疫细胞凋亡导致的。肿瘤免疫反应的下调。我们的数据支持肿瘤来源的TNF-α表达作为肿瘤免疫逃逸机制和恶性进展的重要启动子的作用,并建议对蛋白质(免疫组织化学)或RNA水平(RT-PCR)进行分析可以有效地用于此。尊重。靶向TNF-a可能是一个有前途的选择,尤其是在TNF-a表达高且淋巴结转移阳性的情况下。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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