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Transcription factor Sp1 expression in gastric cancer and its relationship to long-term prognosis

机译:转录因子Sp1在胃癌中的表达及其与长期预后的关系

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摘要

AIM: To explore the expression of Sp1 in gastric carcinoma as well as its association with other clinicopathologic features, and to evaluate the role of Sp1 as a prognostic indicator of gastric carcinoma.METHODS: By using immunohistochemistry, we examined the Sp1 expression patterns in 65 cases of human gastric cancer, and 40 normal gastric mucosa specimens. Simultaneously, the correlation between Sp1 expression and clinical outcome or clinicopathologic features was investigated.RESULTS: The percentage of Sp1 expression was 12.5% (5/40) in normal gastric mucosa, and the Sp1 protein was mainly expressed in the nuclei of cells located in the mucous neck region. In sharp contrast, strong Sp1 expression was detected in tumor cells, whereas no or faint Sp1 staining was detected in stromal cells and normal glandular cells surrounding the tumors. The expression rate of Sp1 in gastric cancer lesions was 53.85% (35/65). The medium survival duration in patients who had a tumor with negative, weak and strong Sp1 expressions was 1700, 1560 and 1026 d, respectively (P<0.05). Sp1 protein expression was closely related to the depth of tumor infiltration (χ2 = 13.223, P<0.01) and TNM stage (χ2 = 11.009, P<0.05), but had no relationship with the number of lymph nodes and Lauren’s classification (P>0.05). Cox regression model for multivariate analysis revealed that high Sp1 expression (P<0.05) and advanced stage (P<0.01) were independent predictors of poor survival.CONCLUSION: Normal and malignant gastric tissues have unique Sp1 expression patterns. Sp1 might serve as an independent prognostic factor, by influencing the tumor infiltration and progression.
机译:目的:探讨Sp1在胃癌中的表达及其与其他临床病理特征的关系,并评估Sp1在胃癌预后中的作用。方法:采用免疫组织化学方法检测65例中Sp1的表达模式。例人类胃癌和40例正常胃黏膜标本。结果:正常胃黏膜中Sp1的表达率为12.5%(5/40),Sp1蛋白主要在胃黏膜上皮细胞核中表达。黏液颈部与之形成鲜明对比的是,在肿瘤细胞中检测到了强烈的Sp1表达,而在肿瘤周围的基质细胞和正常腺细胞中未检测到或仅有淡淡的Sp1染色。 Sp1在胃癌病变中的表达率为53.85%(35/65)。 Sp1阴性,弱和强表达的患者的中位生存期分别为1700、1560和1026 d(P <0.05)。 Sp1蛋白的表达与肿瘤浸润深度(χ 2 = 13.223,P <0.01)和TNM分期(χ 2 = 11.009,P <0.05)密切相关,但与淋巴结数目和劳伦分型无关(P> 0.05)。 Cox回归模型的多变量分析显示,Sp1高表达(P <0.05)和晚期(P <0.01)是不良生存的独立预测因素。结论:正常和恶性胃组织都有独特的Sp1表达模式。 Sp1可能通过影响肿瘤的浸润和进展而成为独立的预后因素。

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