STAT3状态对转移性结肠癌患者RAS和RAF突变的影响

Melin Gecer, Seval Turna, B. Gul, Zuhal Gucin
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引用次数: 0

摘要

目的:结肠腺癌是最常见的胃肠道恶性肿瘤,是世界范围内死亡率和发病率的主要原因之一。STAT3是一种被多种细胞因子和生长因子激活的转录因子,在细胞存活、增殖和分化过程中起着至关重要的作用。在本研究中,我们旨在阐明结肠肿瘤的分子特性。材料与方法:本研究回顾性分析了2016 - 2022年间196例转移性结肠肿瘤患者的KRAS、NRAS和BFAF样本。本机构采用聚合酶链反应(PCR)对样品进行分析。对所有病例进行STAT3免疫组织化学处理,并对染色强度进行分级。结果与肿瘤分子特征、淋巴结状态、分级、位置和直径等预后因素进行比较。结果:196例患者纳入评估,其中女性79例(40.3%),男性117例(59.7%)。STAT3染色强度在人口学特征方面无显著差异。相反,肿瘤分级有统计学意义(p<0.05)。KRAS突变占40.8% (n=80), NRAS突变占2% (n=4), BRAF突变占4.1% (n=8)。测定KRAS与STAT3突变等级之间存在统计学意义相关(p<0.05)。可以看出,KRAS阳性随着患者STAT3染色强度的增加而增加。其他突变结果与STAT3分级之间无统计学意义相关。结论:根据我们的研究结果和先前的文献,已经确定在确定治疗方法之前,常规的STAT3基因筛查是必要的。
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Effect of STAT3 status on RAS & RAF mutation in patients with metastatic colon carcinoma
Objective: Colon adenocarcinomas are the most common gastrointestinal tract malignancy and constitute one of the leading causes of mortality and morbidity worldwide. STAT3 is a transcription factor activated by many cytokines and growth factors and plays a crucial role in cell survival, proliferation, and differentiation. In this research, we aimed to elucidate the molecular properties of colon tumors. Materials & Methods:A total of 196 patients with metastatic colon tumors whose samples were analyzed for KRAS, NRAS, and BFAF between 2016 and 2022 have been investigated in this retrospective study. The samples were analyzed via polymerase chain reaction(PCR)at our institution. STAT3 has been processed to all cases immunohistochemically, and staining intensities were graded.The results were compared with prognostic factors such as tumor molecular characteristics, lymph node status, grade, location, and diameter. Results: A total of 196 patients, 79 (40.3%) female and 117 (59.7%) male, were included in the evaluation within the scope of the study. There was no significant difference between STAT3 staining intensities in terms of demographic characteristics. On the contrary, there was a statistically significant relationship regarding tumor grades (p<0.05). KRAS mutation was found in 40.8% of the patients (n=80), NRAS mutation was found in 2% (n=4), and BRAF mutation was found in 4.1% (n=8). It was determined that there was a statistically significant relationship between KRAS and STAT3 grades of mutations (p<0.05). It is seen that KRAS positivity increases as the STAT3 staining intensity of the patients increases. There was no statistically significant correlation between other mutation results and STAT3 grades. Conclusion:In light of the findings obtained from our study and previous literature, it has been determined that routine STAT3 gene screening is a necessity before the treatment is determined.
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