Georgia State University, Department of Biology, Atlanta, GA, USA.
Emory University School of Medicine, Department of Pathology, Atlanta, GA, USA.
Sci Rep. 2017 Feb 20;7:42289. doi: 10.1038/srep42289.
Nuclear KIFC1 (nKIFC1) predicts worse outcomes in breast cancer, but its prognostic value within racially distinct triple-negative breast cancer (TNBC) patients is unknown. Thus, nKIFC1 expression was assessed by immunohistochemistry in 163 African American (AA) and 144 White TNBC tissue microarrays (TMAs) pooled from four hospitals. nKIFC1 correlated significantly with Ki67 in White TNBCs but not in AA TNBCs, suggesting that nKIFC1 is not merely a surrogate for proliferation in AA TNBCs. High nKIFC1 weighted index (WI) was associated with significantly worse overall survival (OS), progression-free survival (PFS), and distant metastasis-free survival (DMFS) (Hazard Ratios [HRs] = 3.5, 3.1, and 3.8, respectively; P = 0.01, 0.009, and 0.007, respectively) in multivariable Cox models in AA TNBCs but not White TNBCs. Furthermore, KIFC1 knockdown more severely impaired migration in AA TNBC cells than White TNBC cells. Collectively, these data suggest that nKIFC1 WI an independent biomarker of poor prognosis in AA TNBC patients, potentially due to the necessity of KIFC1 for migration in AA TNBC cells.
核 KIFC1(nKIFC1)在乳腺癌中预测预后不良,但在不同种族的三阴性乳腺癌(TNBC)患者中的预后价值尚不清楚。因此,通过免疫组织化学评估了来自 4 家医院的 163 例非裔美国(AA)和 144 例白人 TNBC 组织微阵列(TMA)中 nKIFC1 的表达。nKIFC1 在白人 TNBC 中与 Ki67 显著相关,但在 AA TNBC 中则不然,这表明 nKIFC1 不仅仅是 AA TNBC 增殖的替代物。高 nKIFC1 加权指数(WI)与 AA TNBC 患者的总生存期(OS)、无进展生存期(PFS)和远处转移无复发生存期(DMFS)显著降低显著相关(风险比[HR]分别为 3.5、3.1 和 3.8;P 分别为 0.01、0.009 和 0.007),在多变量 Cox 模型中。此外,KIFC1 敲低在 AA TNBC 细胞中比在白人 TNBC 细胞中更严重地损害迁移。总之,这些数据表明,nKIFC1 WI 是 AA TNBC 患者预后不良的独立生物标志物,这可能是由于 KIFC1 对 AA TNBC 细胞迁移的必要性。