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Expression of midkine and its clinical significance in esophageal squamous cell carcinoma

机译:中期因子在食管鳞癌中的表达及其临床意义

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摘要

AIM: To investigate the expression of midkine in eso-phageal squamous cell carcinoma (ESCC) and analyze its relationship with clinicopathological features.METHODS: RT-PCR and immunocytochemical staining were used to detect the expression of midkine mRNA and protein in EC109 cells, respectively. Then the expression of midkine in 66 cases of ESCC samples were detected by immunohistochemistry using monoclonal antibodies against human midkine.RESULTS: Midkine was expressed in EC109 cell by RT-PCR and immunocytochemistry. The immunoreactivity was detected in 56.1 % (37/66) of the ESCC samples. The expression of midkine was found in cytoplasm of tumor cells. Notably, the intensity of midkine was stronger at the area abundant in vessels and the in-vading border of the tumors. Midkine was more in-tensely expressed in well differentiated tumors (76.9 %) than in moderately and poorly differentiated tumors (43.1 % and 41.2 %, respectively) (P < 0.05). There was no statistically significant correlation between midkine expression and gender, age, clinical stage, lymph node metastasis or survival in ESCC.CONCLUSION: Midkine is overexpressed in ESCC. It may play a role in tumor angiogenesis and invasion. The expression of midkine is correlated with tumor cell differentiation in ESCC. The more poorly tumor cells differentiate, the weaker midkine expresses.
机译:目的:研究中期因子在食管鳞癌中的表达,并分析其与临床病理特征的关系。方法:采用RT-PCR和免疫细胞化学染色技术分别检测中期因子mRNA和蛋白在EC109细胞中的表达。 。然后用抗人中期因子的单克隆抗体通过免疫组织化学方法检测66例ESCC样品中中期因子的表达。结果:RT-PCR和免疫细胞化学法检测EC109细胞中的中期因子的表达。在56.1%(37/66)的ESCC样品中检测到免疫反应性。在肿瘤细胞的细胞质中发现了midkine的表达。值得注意的是,在血管丰富的区域和肿瘤的侵入边界,中期因子的强度较强。 Midkine在高分化肿瘤中的表达强度更高(76.9%),而在中低分化肿瘤中的表达强度更高(分别为43.1%和41.2%)(P <0.05)。结论:胚胎干细胞中中期因子的表达与性别,年龄,临床分期,淋巴结转移或生存率无统计学意义。结论:胚胎干细胞中中期因子的表达过高。它可能在肿瘤血管生成和侵袭中起作用。中期因子的表达与ESCC中的肿瘤细胞分化有关。肿瘤细胞分化越差,中因子表达越弱。

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