Department of Pathology, Habib Bourguiba University Hospital, Sfax, Tunisia.
Department of Pathology, Habib Bourguiba University Hospital, Sfax, Tunisia.
Ann Diagn Pathol. 2020 Dec;49:151624. doi: 10.1016/j.anndiagpath.2020.151624. Epub 2020 Sep 4.
Mucinous colorectal carcinoma (MC) is a rare subtype of colorectal adenocarcinoma known to be associated with bad prognosis. Lately, research has turned to identify new prognostic markers allowing the use of targeted therapy. The aim of our study is to evaluate the prognostic impact of E-cadherin and Cox-2expression in MC.
A total of 40 formalin-fixed, paraffin-embedded MC specimens were collected within a period of 13 years and were studied for the expression of the two proteins. We used SPSS 22 software to study associations with clinicopathological parameters and overall survival (OS).
A reduced or absent E-cadherin expression was noted in 52.5% of cases. It was associated with distant metastases (p = 0.049) and venous invasion (p = 0.049). Cox-2 was overexpressed in 17.5% of cases. It was associated with negative lymph node status (p = 0.020) and with early stage tumor (p = 0.020). A significant association between the two proteins was also noted (p = 0.04). No significant association with OS was found; However, there was an improvement in the survival of patients overexpressing Cox-2 (p = 0.16).
Our findings link the loss of E-cadherin expression with spread and aggressiveness in MC and Cox-2 overexpression with better prognosis and survival. Because MC has a distinct genetic pathway we encourage the analysis of MSI and Cox-2 expression in all MC. Cox-2 inhibitors may not be effective chemopreventative agents in the setting of defective DNA mismatch repair. More molecular studies are needed to better understand the role of these markers and their prognostic significance in MC.
黏液性结直肠癌(MC)是一种罕见的结直肠腺癌亚型,已知与不良预后相关。最近,研究已经转向识别新的预后标志物,以允许使用靶向治疗。我们的研究目的是评估 E-钙黏蛋白和 Cox-2 表达在 MC 中的预后影响。
在 13 年的时间内收集了总共 40 例福尔马林固定、石蜡包埋的 MC 标本,并对这两种蛋白质的表达进行了研究。我们使用 SPSS 22 软件研究与临床病理参数和总生存期(OS)的关联。
52.5%的病例中观察到 E-钙黏蛋白表达减少或缺失。它与远处转移(p=0.049)和静脉侵犯(p=0.049)相关。Cox-2 在 17.5%的病例中过表达。它与阴性淋巴结状态(p=0.020)和早期肿瘤(p=0.020)相关。还观察到两种蛋白质之间存在显著关联(p=0.04)。与 OS 无显著关联;然而,Cox-2 过表达的患者的生存率有所提高(p=0.16)。
我们的研究结果将 E-钙黏蛋白表达缺失与 MC 的扩散和侵袭性联系起来,Cox-2 过表达与更好的预后和生存相关。因为 MC 具有独特的遗传途径,我们鼓励在所有 MC 中分析 MSI 和 Cox-2 表达。在 DNA 错配修复缺陷的情况下,Cox-2 抑制剂可能不是有效的化学预防剂。需要更多的分子研究来更好地了解这些标志物在 MC 中的作用及其预后意义。