Djikic Rom Aleksandra, Dragicevic Sandra, Jankovic Radmila, Radojevic Skodric Sanja, Sabljak Predrag, Markovic Velimir, Stojkovic Jovana Rosic, Barisic Goran, Nikolic Aleksandra
Department of Pathology, Pathohistology and Medical Cytology, University Clinical Center of Serbia, Pasterova 2, 11000 Belgrade, Serbia.
Gene Regulation in Cancer Group, Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, 11000 Belgrade, Serbia.
Diagnostics (Basel). 2024 Jul 13;14(14):1512. doi: 10.3390/diagnostics14141512.
Approximately 20% of patients with colorectal cancer (CRC) are diagnosed with a mucinous subtype of this tumor, have a worse prognosis, and often show resistance to available therapies. Molecules from the mucin family are involved in the regulation of epithelial-mesenchymal transition (EMT), which significantly determines the cancer aggressiveness. This study aimed to examine the diagnostic and prognostic significance of mucinous histology and EMT markers in patients with early-onset CRC and their association with disease severity and tumor characteristics. This study included tumor tissue samples from 106 patients diagnosed with CRC before the age of 45, 53 with mucinous and 53 with non-mucinous tumors. The EMT status was determined by immunohistochemical analysis of E-cadherin and Vimentin in tissue sections. Mucinous tumors had significantly higher Mucin-1 ( < 0.001) and cytoplasmic E-cadherin ( = 0.043) scores; they were significantly less differentiated ( = 0.007), more advanced ( = 0.027), and predominately affected right the colon ( = 0.039) compared to non-mucinous tumors. Epithelial tumors were significantly better differentiated ( = 0.034) and with less prominent tumor budding ( < 0.001) than mesenchymal tumors. Mucin-1 and Vimentin were independent predictors of tumor differentiation ( = 0.006) and budding ( = 0.001), respectively. Mucinous histology and EMT markers are significant predictors of disease severity and tumor characteristics in early-onset colorectal cancer.
约20%的结直肠癌(CRC)患者被诊断为该肿瘤的黏液亚型,预后较差,且常对现有治疗产生耐药性。黏蛋白家族分子参与上皮-间质转化(EMT)的调控,而EMT在很大程度上决定了癌症的侵袭性。本研究旨在探讨黏液组织学和EMT标志物在早发性CRC患者中的诊断和预后意义,以及它们与疾病严重程度和肿瘤特征的关联。本研究纳入了106例45岁之前被诊断为CRC的患者的肿瘤组织样本,其中53例为黏液性肿瘤,53例为非黏液性肿瘤。通过对组织切片中的E-钙黏蛋白和波形蛋白进行免疫组化分析来确定EMT状态。与非黏液性肿瘤相比,黏液性肿瘤的黏蛋白-1(<0.001)和细胞质E-钙黏蛋白(=0.043)评分显著更高;它们的分化程度显著更低(=0.007),分期更晚(=0.027),且主要累及右半结肠(=0.039)。上皮性肿瘤的分化程度显著优于间质性肿瘤(=0.034),肿瘤芽生也不那么明显(<0.001)。黏蛋白-1和波形蛋白分别是肿瘤分化(=0.006)和芽生(=0.001)的独立预测因子。黏液组织学和EMT标志物是早发性结直肠癌疾病严重程度和肿瘤特征的重要预测指标。