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Expression of EPHRIN-A1, SCINDERIN and MHC class I molecules in head and neck cancers and relationship with the prognostic value of intratumoral CD8 + T cells

机译:EPHRIN-A1,SCINDERIN和MHC I类分子在头颈癌中的表达及其与肿瘤内CD8 + T细胞预后的关系

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Background Our group has previously shown that EPHRIN-A1 and SCINDERIN expression by tumor cells rendered them resistant to cytotoxic T lymphocyte-mediated lysis. Whereas the prognostic value of EPHRIN-A1 expression in cancer has already been studied, the role of SCINDERIN presence remains to be established. In the present work, we investigated the prognosis value of EPHRIN-A1 and SCINDERIN expression in head and neck carcinomas. In addition, we monitored the HLA-class I expression by tumor cells and the presence of tumor-infiltrating CD8+ T cells to evaluate a putative correlation between these factors and the survival prognosis by themselves or related to EPHRIN-A1 and SCINDERIN expression. Methods Tumor tissue sections of 83 patients with head and neck cancer were assessed by immunohistochemistry for the expression of EPHRIN-A1, SCINDERIN, HLA class I molecules and the presence of CD8+ T cells. Results No significant prognosis value could be attributed to these factors independently, despite a tendency of association between EPHRIN-A1 and a worse clinical outcome. No prognostic value could be observed when CD8+ T cell tumor infiltration was analyzed combined with EPHRIN-A1, SCINDERIN or HLA class I expression. Conclusion These results highlight that molecules involved in cancer cell resistance to cytotoxic T lymphocytes by themselves are not a sufficient criteria for prognosis determination in cancer patients. Other intrinsic or tumor microenvironmental features should be considered in prognostic evaluation.
机译:背景我们的研究小组先前已证明肿瘤细胞表达EPHRIN-A1和SCINDERIN使其对细胞毒性T淋巴细胞介导的裂解具有抗性。尽管已经研究了EPHRIN-A1表达在癌症中的预后价值,但SCINDERIN存在的作用尚待确定。在目前的工作中,我们调查了EPHRIN-A1和SCINDERIN在头颈癌中的预后价值。此外,我们监测了肿瘤细胞的HLA-I类表达以及肿瘤浸润性CD8 + T细胞的存在,以评估这些因素与它们自身或与EPHRIN相关的生存预后之间的推测相关性。 -A1和SCINDERIN表达。方法采用免疫组织化学方法检测83例头颈癌患者的肿瘤组织切片中EPHRIN-A1,SCINDERIN,HLA I类分子的表达及CD8 + T细胞的表达。结果尽管EPHRIN-A1与较差的临床结局之间存在关联的趋势,但没有独立地将这些因素独立地归为重要的预后价值。当结合EPHRIN-A1,SCINDERIN或HLA I类表达分析CD8 + T细胞肿瘤浸润时,未观察到预后价值。结论这些结果表明,与癌细胞对细胞毒性T淋巴细胞的抗性有关的分子本身并不是确定癌症患者预后的充分标准。在预后评估中应考虑其他固有的或肿瘤的微环境特征。

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