Niknami Zohreh, Muhammadnejad Ahad, Ebrahimi Alireza, Harsani Zahra, Shirkoohi Reza
Department of Genetics, Faculty of Science, Islamic Azad University, Damghan, Iran.
Cancer Biology Research Center, Cancer Institute of Iran, Tehran University of Medical Sciences, Tehran, Iran.
EXCLI J. 2020 Jun 26;19:917-926. doi: 10.17179/excli2020-1946. eCollection 2020.
Colorectal cancer is the most common malignancy of the gastrointestinal tract with very high mortality. One of the most distinguishing features for the establishment of an epithelial-mesenchymal transition phenotype is the alteration of mesenchymal markers and structural adhesion proteins. We investigated the level of Vimentin and E-cadherin expression in relation to invasion and metastasis on colorectal cancer patients. Tissue specimens were collected consecutively from thirty-nine colorectal carcinoma patients during surgeries. The patients were diagnosed and treated between 2013 and 2016. In order to histological staging, tissue sections were prepared from formalin-fixed paraffin-embedded blocks and stained with Hematoxylin and Eosin. Also for evaluating the epithelial-mesenchymal transition markers, E-cadherin and Vimentin, all patient samples were stained and detected via immunohistochemistry, and afterwards the results were analyzed to determine whether these markers could be useful prognostic markers for predicting colorectal cancer patient outcomes. The expression of Vimentin as a mesenchymal marker along with rising grade of cancer, pathological stages, and metastasis to regional lymph nodes increased furthermore, in cancers with vascular invasion, Vimentin value was high. Reversely, the expression of E-cadherin with climbing grade, stages and colon cancer categories decreased and also in cancers with vascular invasion reduced. Variation of the markers had no relation to age and sex. In summary, along with cancer progression level of Vimentin expression varies inversely with E-cadherin expression and by increasing metastasis and invasion the Vimentin expression elevates. Further evaluation in this area might lead to a good method for predicting progressive clone cancer.
结直肠癌是胃肠道最常见的恶性肿瘤,死亡率很高。上皮-间质转化表型确立的最显著特征之一是间质标志物和结构粘附蛋白的改变。我们研究了结直肠癌患者中波形蛋白和E-钙粘蛋白的表达水平与侵袭和转移的关系。在手术过程中连续收集了39例结直肠癌患者的组织标本。这些患者在2013年至2016年期间被诊断和治疗。为了进行组织学分期,从福尔马林固定石蜡包埋块制备组织切片,并用苏木精和伊红染色。同样为了评估上皮-间质转化标志物E-钙粘蛋白和波形蛋白,所有患者样本均通过免疫组织化学进行染色和检测,然后分析结果以确定这些标志物是否可作为预测结直肠癌患者预后的有用预后标志物。波形蛋白作为一种间质标志物的表达随着癌症分级、病理分期以及区域淋巴结转移的增加而进一步升高,在有血管侵犯的癌症中,波形蛋白值较高。相反,E-钙粘蛋白的表达随着分级、分期和结肠癌类型的升高而降低,在有血管侵犯的癌症中也降低。这些标志物的变化与年龄和性别无关。总之,随着癌症进展,波形蛋白的表达水平与E-钙粘蛋白的表达呈负相关,并且随着转移和侵袭的增加,波形蛋白的表达升高。在这一领域的进一步评估可能会带来一种预测进展性克隆癌的良好方法。