Department of Immuno-Histo-Cytology, Salah Azaiez Institute, Tunis 1006, Tunisia; Department of Biology, Laboratory of Mycology, Pathologies and Biomarkers (LR16ES05), Faculty of Sciences of Tunis, University of Tunis El Manar, Tunis 2092, Tunisia.
Department of Immuno-Histo-Cytology, Salah Azaiez Institute, Tunis 1006, Tunisia; Department of Biology, Laboratory of Mycology, Pathologies and Biomarkers (LR16ES05), Faculty of Sciences of Tunis, University of Tunis El Manar, Tunis 2092, Tunisia.
Ann Diagn Pathol. 2022 Aug;59:151954. doi: 10.1016/j.anndiagpath.2022.151954. Epub 2022 Apr 22.
Zinc finger E-box binding homeobox factor 1 (ZEB1) is a transcription factor involved in the epithelial to mesenchymal transition (EMT) process of metaplastic breast cancer (MBC). This study aimed to assess the expression of ZEB1 in MBC and explore its association with clinicopathological factors and prognosis. We analyzed the immunohistochemical expression of ZEB1 in 50 MBC tissue samples. ZEB1 was overexpressed in 36% (18/50) of cases. ZEB1 overexpression was significantly correlated to fibromatosis-like and spindle cell sarcoma subtypes (P < 0.001) and tended to be correlated to metastatic status (P = 0.069). Using the Kaplan-Meier method, ZEB1 expression was significantly associated with poor 5-years overall survival (OS) (P = 0.001) and relapse-free survival (RFS) (P = 0.0001). The multivariate Cox regression analysis showed that ZEB1 positive remained a significantly independent adverse prognostic factor for RFS and OS (HR = 4.9 [2.14-11.53]; P < 0.0001) and (HR = 4 [1.05-15.18]; P = 0.042), while Vimentin was an independent poor prognostic factor only for RFS (HR = 5.69 [1.79-18.11], P = 0.003). Our results indicated that ZEB1 and Vimentin overexpression might serve as adverse prognostic factors and potential therapeutic targets for MBC patients.
锌指 E 盒结合同源盒因子 1(ZEB1)是一种参与癌肉瘤中上皮间质转化(EMT)过程的转录因子。本研究旨在评估 ZEB1 在癌肉瘤中的表达,并探讨其与临床病理因素和预后的关系。我们分析了 50 例癌肉瘤组织标本中 ZEB1 的免疫组织化学表达。ZEB1 在 36%(18/50)的病例中过表达。ZEB1 过表达与纤维瘤样和梭形细胞肉瘤亚型显著相关(P<0.001),并倾向于与转移状态相关(P=0.069)。Kaplan-Meier 法显示,ZEB1 表达与 5 年总生存(OS)(P=0.001)和无复发生存(RFS)(P=0.0001)显著相关。多因素 Cox 回归分析显示,ZEB1 阳性仍然是 RFS 和 OS 的显著独立不良预后因素(HR=4.9[2.14-11.53];P<0.0001)和(HR=4[1.05-15.18];P=0.042),而波形蛋白仅为 RFS 的独立不良预后因素(HR=5.69[1.79-18.11],P=0.003)。我们的结果表明,ZEB1 和波形蛋白的过表达可能成为癌肉瘤患者的不良预后因素和潜在治疗靶点。