首页|DNA错配修复系统与早发结直肠癌的相关性研究

DNA错配修复系统与早发结直肠癌的相关性研究

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为探讨DNA错配修复(MMR)系统与早发性结直肠癌(EO-CRC)病理特征及其预后关系,收集189例EO-CRC肿瘤组织.通过免疫组化方法分为完整型组(pMMR)和缺陷型组(dMMR);基于Kaplan-Meier方法分析两组预后现状.研究结果显示,37例样本为dM-MR,152例样本为pMMR.dMMR组中,MLH1和PMS2同时缺失最多(32.43%);dM-MR组肿瘤位置大多发生于右半结肠(48.65%),pMMR组大多发生于直肠(58.55%);两组肿瘤尺寸大小和TNM分期均具有统计学意义(P<0.05);两组整体生存率具有统计学意义(Log-rank x2=4.19,P<0.05).这表明,EO-CRC患者中dMMR组具有特殊的病理特征且预后更好,为EO-CRC患者的早期诊断和精准治疗提供参考.
Study on the Correlation Between the DNA Mismatch Repair System and Early-onset Colorectal Cancer
To investigate the relationship between DNA mismatch repair(MMR)system and the pathologi-cal features and prognosis of early-onset colorectal cancer(EO-CRC),189 EO-CRC tumor tissues were collected and divided into proficient group(pMMR)and defective group(dMMR)by immunohistochemis-try.The prognosis status of the two groups was analyzed by Kaplan-Meier method.The results show that 37 samples are dMMR and 152 samples are pMMR.MLH1 and PMS2 are most missing(32.43%)in the dMMR group.The tumor location in the dMMR group is mostly in the right half of the colon(48.65%),while the tumor location in the pMMR group is mostly in the rectum(58.55%).The data of tumor size and TNM stage are statistically different(P<0.05),and the overall survival is statistically different(Log-rank x2=4.19,P<0.05)between the two groups.This indicates that the dMMR group among EO-CRC patients has special pathological characteristics and a better prognosis,providing references for the early diagnosis and precise treatment of EO-CRC patients.

mismatch repair proteinearly-onset colorectal cancermicrosatellite instabilityimmunohisto-chemistry

王玉娥、孙运军、杨桂丽、张晓红、张敏、高敏敏、刘福国

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青岛大学附属医院消化内科,青岛 266071

临沂市肿瘤医院特检科内镜室,临沂 276000

菏泽市牡丹区中医医院内科,菏泽 274000

错配修复蛋白 早发性结直肠癌 微卫星不稳定 免疫组织化学

2024

青岛大学学报(自然科学版)
青岛大学

青岛大学学报(自然科学版)

影响因子:0.248
ISSN:1006-1037
年,卷(期):2024.37(3)