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IMP3免疫组化表达在三阴性乳腺癌中的预后价值

Prognostic value of IMP3 immunohistochemical expression in triple negative breast cancer.

作者信息

Sjekloča Nikoleta, Tomić Snjezana, Mrklić Ivana, Vukmirović Filip, Vučković Ljiljana, Lovasić Ingrid Belas, Maras-Šimunić Marina

机构信息

Medical Faculty, University of Montenegro, Montenegro.

Department of Pathology, Forensic Medicine and Cytology, University Hospital Split.

出版信息

Medicine (Baltimore). 2020 Feb;99(7):e19091. doi: 10.1097/MD.0000000000019091.

Abstract

Triple negative breast cancer (TNBC) account for 12% to 17% of all breast cancers. It is a heterogeneous group of tumors associated with aggressive clinical course. Insulin-like growth factor II mRNA binding protein 3 (IMP3) belongs to a family of insulin-like growth factor type II (IGF2), which plays a key role in the transmission and stabilization of mRNA, cell growth, and migration during embryogenesis. Increased expression of IMP3 is associated with aggressive behavior of different tumor types, advanced clinical stage, distant metastasis, and shorter overall survival (OS).The study included 118 patients with breast carcinoma diagnosed as TNBC and immunohistochemical staining for estrogen receptors (ER), progesterone receptors (PR), epidermal growth factor receptor 2 (HER2/neu), Ki-67, and IMP3 was performed. Correlations between categorical variables were studied using the chi-square and the Mann-Whitney U test. For survival analysis, the Kaplan-Meier method, log-rank test and the Cox proportional hazard regression model were used.Positive expression of IMP3 protein was present in 35.6% of TNBC. The presence of basal morphology was observed in 46.6% of TNBC. Positive IMP3 expression was connected with larger size of tumor, higher clinical stage, and basal morphology (P = .039, P = .034, P < .001). Disease-free survival and OS were significantly shorter in IMP3 positive TNBC.According to results of our study IMP3 expression can be used as negative prognostic factor for triple negative breast carcinomas. Targeting IMP3 molecule could be an effective approach to the management of a triple negative breast cancer with new immunological therapies, which does not yet exist for this group of tumors.

摘要

三阴性乳腺癌(TNBC)占所有乳腺癌的12%至17%。它是一组异质性肿瘤,与侵袭性临床病程相关。胰岛素样生长因子II mRNA结合蛋白3(IMP3)属于胰岛素样生长因子II型(IGF2)家族,在胚胎发育过程中mRNA的传递和稳定、细胞生长及迁移中起关键作用。IMP3表达增加与不同肿瘤类型的侵袭性行为、临床晚期、远处转移及较短的总生存期(OS)相关。该研究纳入了118例诊断为TNBC的乳腺癌患者,并对雌激素受体(ER)、孕激素受体(PR)、表皮生长因子受体2(HER2/neu)、Ki-67和IMP3进行了免疫组化染色。使用卡方检验和曼-惠特尼U检验研究分类变量之间的相关性。生存分析采用Kaplan-Meier法、对数秩检验和Cox比例风险回归模型。IMP3蛋白阳性表达在35.6%的TNBC中存在。46.6%的TNBC观察到基底样形态。IMP3阳性表达与肿瘤较大、临床分期较高及基底样形态相关(P = 0.039,P = 0.034,P < 0.001)。IMP3阳性的TNBC无病生存期和总生存期显著缩短。根据我们的研究结果,IMP3表达可作为三阴性乳腺癌的负面预后因素。靶向IMP3分子可能是一种有效的方法,用于采用新的免疫疗法治疗三阴性乳腺癌,而目前针对这组肿瘤尚无此类疗法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f26/7035046/30e7156ceb3c/medi-99-e19091-g001.jpg

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