Alina Elena Ciobanu, Cristina Maria Marginean, Cristian Mesina, Tudor-Adrian Balseanu, Daniela Ciobanu, Mirela Marinela Florescu
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引用次数: 0
摘要
错配修复(MMR)蛋白的缺乏是结直肠癌发生的分子途径之一,这可能对预测治疗成功率产生重大临床影响。本研究旨在分析91例结直肠癌(CRC)患者中MutL同源物1(MLH1)、MutS同源物2(MSH2)和MutS同源物6(MSH6)的表达情况,并评估患者临床病理特征与这些生物标志物的免疫表达之间的关系。在这项研究中,我们发现非黏液性肿瘤、中度分化病变和 IV 期患者的 MLH1 免疫表达得分最高。MSH2和MSH6的最高值分别出现在粘液性肿瘤、分化不良病变、II-III期和III-IV期。为了改进肿瘤靶向治疗的分层标准并预测患者的预后,所使用的标记物可能有助于评估病变的侵袭性。
Immunoexpression of Mismatch Repair Proteins in a Cohort of Colorectal Cancer Patients.
One of the molecular routes of colorectal carcinogenesis is the lack of mismatch repair (MMR) proteins, which may have substantial clinical consequences in predicting therapy success. This study aimed to analyze the expression of the MutL homolog 1 (MLH1), MutS homolog 2 (MSH2), and MutS homolog 6 (MSH6) in a cohort of 91 colorectal cancer (CRC) patients, and to evaluate the relationship between patient clinicopathological characteristics and immunoexpression of these biomarkers. In this study, we obtained the highest scores of the MLH1 immunoexpression in non-mucinous tumors, moderately differentiated lesions, and in stage IV. The highest values of the MSH2 and MSH6 scores were observed in mucinous tumors, and poorly differentiated lesions, in stages II-III, and stages III-IV, respectively. To improve the stratification criteria for targeted oncological therapy and to predict patient outcomes, markers used may help evaluate the aggressiveness of lesions.