胃腺癌生物标志物表达谱及其预后价值。

S. Şenol, A. Aydın, Duygu Kosemetin, D. Ece, I. Akalın, Hasan Abuoğlu, Esra Akdeniz Duran, D. Aydın, Burçak Erkol
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引用次数: 7

摘要

通过免疫组织化学染色检测了几种与癌变有关的分子的表达水平,并评估了它们在胃腺癌(GA)中的表达水平对预后的意义。通过免疫组织化学方法对115个GA和20个对照胃组织样本进行了评估,使用33种抗体靶向已知在各种肿瘤发展中起作用的分子。GA患者中碳酸酐酶IX (CAIX)的过表达和富含at的相互作用结构域蛋白1A (ARID1A)、醛脱氢酶1 (ALDH1)和CD44表达的缺失与淋巴结(LN)转移、肿瘤分期晚期和不良预后显著相关。结果表明,ALDH1A和ARID1A可能是影响总生存率和无复发生存率的独立预后因素(p < 0.01和p < 0.05)。我们的研究结果表明,与对照细胞相比,免疫反应性GA肿瘤细胞中的ALDH1、CD44、ARID1A和CAIX表现出不同的表达谱,这些差异与患者的生存有关。具有差异表达谱的分子与一些常见功能相关,包括缺氧、上皮-间质转化和SW1/ snf介导的染色质重塑。此外,ALDH1、ARID1A和CD44的缺失以及CAIX的过表达对肿瘤的侵袭和转移也很重要;因此,它们可以作为GA患者长期生存的有用预后指标。综上所述,我们的研究发现GA肿瘤细胞中评估的一些蛋白的异常表达可能在GA的癌变和肿瘤进展中起重要作用,从而可能影响GA患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gastric Adenocarcinoma Biomarker Expression Profiles and their Prognostic Value.
Expression levels of several molecules implicated in carcinogenesis were examined by immunohistochemical staining, and the prognostic significance of their expression levels in gastric adenocarcinoma (GA) was evaluated. A total of 115 GA and 20 control gastric tissue samples were evaluated by immunohistochemistry using 33 antibodies targeting molecules known to play a part in the development of various tumors. Overexpression of carbonic anhydrase IX (CAIX) and loss of AT-rich interactive domain-containing protein 1A (ARID1A), aldehyde dehydrogenase 1 (ALDH1), and CD44 expression in GA patients were significantly correlated with lymph node (LN) metastasis, advanced tumor stage, and poor prognosis. The results demonstrated that ALDH1A and ARID1A may be strong independent prognostic factors associated with overall survival and recurrence-free survival (p < 0.01 and p < 0.05, respectively). Our results demonstrated that ALDH1, CD44, ARID1A, and CAIX in immunoreactive GA tumor cells exhibit different expression profiles compared with control cells and that these differences are associated with patient survival. The molecules with differential expression profiles were associated with some common functions, including hypoxia, epithelial-to-mesenchymal transition, and SW1/SNF-mediated chromatin remodeling. In addition, the loss of ALDH1, ARID1A, and CD44 and the overexpression of CAIX are important for tumor invasion and metastasis; therefore, they may serve as useful prognostic indicators of long-term survival in patients with GA. In conclusion, our study found that abnormal expression of some of the proteins evaluated in GA tumor cells might have an important role in carcinogenesis and tumor progression and thus may influence the prognosis of patients with GA.
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