摘要
目的探讨分泌性卷曲相关蛋白4(SFRP4)、高迁移率族蛋白B1(HMGB1)、DEP结构域蛋白1B(DEPDC1B)、程序性死亡蛋白配体-1(PD-L1)在三阴性乳腺癌(TNBC)组织中表达意义。方法选取83例TNBC患者作为研究对象,均于术中采集肿瘤组织及癌旁正常组织,采用免疫组化SP法检测SFRP4、HMGB1、DEPDC1B及PD-L1表达情况,比较肿瘤组织及正常组织内上述表达情况;并分析SFRP4、HMGB1、DEPDC1B及PD-L1表达与患者年龄、绝经状态、肿瘤直径、淋巴结转移、肿瘤分期等病理特征的关系。结果肿瘤组织内SFRP4、HMGB1、DEPDC1B及PD-L1阳性表达率高于正常组织,差异有统计学意义(P<0.05);SFRP4、HMGB1、DEPDC1B及PD-L1阳性表达患者肿瘤直径≥3 cm、临床分期Ⅲ~Ⅳ期、有淋巴结转移占比高于SFRP4、HMGB1、DEPDC1B及PD-L1阴性表达患者,差异有统计学意义(P<0.05)。结论SFRP4、HMGB1、DEPDC1B及PD-L1在TNBC组织内存在较高表达,且高表达与肿瘤分期、淋巴结转移关系密切,可用于指导临床完善治疗方案。
Objective To investigate the expression significance of secreted crimp-associated protein 4(SFRP4),high mobility group protein B1(HMGB1),DEP domain protein 1B(DEPDC1B),programmed death protein ligand-1(PD-L1)in triple negative breast cancer(TNBC)tissues.Methods 83 patients with TNBC were selected as the study objects.Tumor tissues and adjacent normal tissues were collected during the operation.The expression of SFRP4,HMGB1,DEPDC1B and PD-L1 were detected by immunohistochemical SP method.The relationship between the expression of SFRP4,HMGB1,DEPDC1B and PD-L1 and the pathological characteristics of patients such as age,menopause,tumor diameter,lymph node metastasis and tumor stage was analyzed.Results The positive expression rates of SFRP4,HMGB1,DEPDC1B and PD-L1 in tumor tissues were higher than those in normal tissues,and the difference was statistically significant(P<0.05).Patients with positive expression of SFRP4,HMGB1,DEPDC1B and PD-L1 had tumor diameter≥3 cm,clinical stageⅢ~Ⅳ,and the proportion of lymph node metastasis was higher than those with negative expression of SFRP4,HMGB1,DEPDC1B and PD-L1,and the difference was statistically significant(P<0.05).Conclusion SFRP4,HMGB1,DEPDC1B and PD-L1 are highly expressed in TNBC tissues,and the high expression is closely related to tumor stage and lymph node metastasis,which can be used to guide clinical improvement of treatment.
作者
付刚
封琳
FU Gang;FENG Lin(The Second People's Hospital of Jiaozuo,Jiaozuo,454000)
出处
《实用癌症杂志》
2024年第11期1774-1776,1781,共4页
The Practical Journal of Cancer