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CXCL16 和 CXCR6 在尤文肉瘤家族肿瘤中的表达。

CXCL16 and CXCR6 in Ewing sarcoma family tumor.

机构信息

Department of Pathology, Graduate School of Medicine, Kyung Hee University, Seoul, South Korea.

Department of Biomedical Science, College of Health Science, Korea University, Seoul, South Korea.

出版信息

Hum Pathol. 2014 Apr;45(4):753-60. doi: 10.1016/j.humpath.2013.09.017. Epub 2013 Nov 21.

Abstract

Chemokines are a family of peptide mediators that play an essential role in cellular migration and intracellular communication in tumor cells as well as immune cells. We hypothesized that the CXCL16-CXCR6 ligand-receptor system plays an important role in Ewing sarcoma (ES) family tumor (ESFT) progression. Using real-time quantitative reverse transcription-polymerase chain reaction, we investigated the mRNA expression of CXCL16, CXCR6, and ADAM 10 in various cell lines. We also investigated the expression of CXCL16, CXCR6, ADAM 10, and ADAM 17 in tissue samples from 61 ESFT patients using immunohistochemistry. The mRNA expression levels of CXCL16 and CXCR6 in the ES cell line were higher than those in the other cell lines. Immunohistochemical staining revealed that CXCL16 and CXCR6 were highly expressed in tumor cells of ESFT and showed a positive correlation between them. The expression of CXCL16 and CXCR6 was associated with the occurrence of lung metastasis. Univariate analysis revealed that CXCL16 or CXCR6 expression was associated with worse prognosis of ESFT patients. In addition, CXCL16 and CXCR6 expression was associated with shorter overall survival irrespective of other prognostic factors. Our results suggest that the CXCL16/CXCR6 axis appears to be important in the progression of ESFT, resulting in more aggressive clinical behavior. Furthermore, there may be a decrease in the overall survival in ESFT patients who have tumors that stain strongly for CXCL16 and CXCR6.

摘要

趋化因子是一类肽介质,在肿瘤细胞和免疫细胞的细胞迁移和细胞内通讯中发挥重要作用。我们假设 CXCL16-CXCR6 配体-受体系统在尤文肉瘤(ES)家族肿瘤(ESFT)进展中发挥重要作用。我们使用实时定量逆转录聚合酶链反应,研究了各种细胞系中 CXCL16、CXCR6 和 ADAM10 的 mRNA 表达。我们还使用免疫组织化学法研究了 61 例 ESFT 患者组织样本中 CXCL16、CXCR6、ADAM10 和 ADAM17 的表达。ES 细胞系中 CXCL16 和 CXCR6 的 mRNA 表达水平高于其他细胞系。免疫组织化学染色显示 CXCL16 和 CXCR6 在 ESFT 的肿瘤细胞中高度表达,并呈正相关。CXCL16 和 CXCR6 的表达与肺转移的发生有关。单因素分析显示,CXCL16 或 CXCR6 的表达与 ESFT 患者的预后不良相关。此外,无论其他预后因素如何,CXCL16 和 CXCR6 的表达与总生存期较短相关。我们的结果表明,CXCL16/CXCR6 轴似乎在 ESFT 的进展中很重要,导致更具侵袭性的临床行为。此外,在 CXCL16 和 CXCR6 染色强阳性的肿瘤患者中,ESFT 患者的总生存率可能会降低。

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