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环氧化酶2的高表达是接受艾弗·刘易斯食管切除术后的食管鳞状细胞癌患者的预后指标。

High expression of cyclooxygenase 2 is an indicator of prognosis for patients with esophageal squamous cell carcinoma after Ivor Lewis esophagectomy.

作者信息

Hu Dongxin, Zhang Mingyan, Wang Shuai, Wang Zhou

机构信息

Department of Thoracic Surgery Provincial Hospital Affiliated to Shandong University Jinan Shandong China.

Department of Gastroenterology Provincial Hospital Affiliated to Shandong University Jinan Shandong China.

出版信息

Thorac Cancer. 2016 Apr 26;7(3):310-5. doi: 10.1111/1759-7714.12329. Epub 2016 Jan 4.

Abstract

BACKGROUND

The poor prognosis of esophageal squamous cell carcinoma (ESCC) is attributed to a high recurrence rate after surgery. Cyclooxygenase 2 (COX2) is an important regulator of cell growth, differentiation, apoptosis, and transformation. COX2 overexpression is significantly associated with the tumorigenesis and progression of diverse cancers; however, its expression and significance in ESCC remains unclear.

METHODS

We enrolled 118 patients with ESCC who had undergone Ivor-Lewis esophagectomy. The expression profile of COX2 was examined by immunohistochemistry.

RESULTS

A high expression of COX2 correlated with a higher T staging (P = 0.014), lower differentiation degree (P = 0.002), lymph node metastasis (P = 0.009), recurrence status (P = 0.004), and tumor node metastasis (TNM) stage (P = 0.001). Cox regression analysis showed that TNM stage (P = 0.001), differentiation degree (P = 0.001), and high COX2 expression (P = 0.004) were independent risk factors of prognosis.

CONCLUSION

Our data indicated that COX2 expression level is associated with key clinicopathological features and could be an effective biomarker to predict ESCC prognosis.

摘要

背景

食管鳞状细胞癌(ESCC)预后较差,原因是手术后复发率高。环氧合酶2(COX2)是细胞生长、分化、凋亡和转化的重要调节因子。COX2过表达与多种癌症的发生和进展显著相关;然而,其在ESCC中的表达及意义仍不明确。

方法

我们纳入了118例行Ivor-Lewis食管切除术的ESCC患者。通过免疫组织化学检测COX2的表达情况。

结果

COX2高表达与较高的T分期(P = 0.014)、较低的分化程度(P = 0.002)、淋巴结转移(P = 0.009)、复发状态(P = 0.004)和肿瘤淋巴结转移(TNM)分期(P = 0.001)相关。Cox回归分析显示,TNM分期(P = 0.001)、分化程度(P = 0.001)和COX2高表达(P = 0.004)是预后的独立危险因素。

结论

我们的数据表明,COX2表达水平与关键的临床病理特征相关,可能是预测ESCC预后的有效生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98a6/4846619/a53a829f61d0/TCA-7-310-g001.jpg

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