Centre for Cancer Biomarkers CCBIO, Department of Clinical Medicine, Section for Pathology, University of Bergen, Bergen, Norway.
Department of Pathology, Haukeland University Hospital, Bergen, Norway.
Sci Rep. 2017 Apr 24;7(1):1089. doi: 10.1038/s41598-017-00862-w.
We here examined whether Nestin, by protein and mRNA levels, could be a predictor of BRCA1 related breast cancer, a basal-like phenotype, and aggressive tumours. Immunohistochemical staining of Nestin was done in independent breast cancer hospital cohorts (Series I-V, total 1257 cases). Also, TCGA proteomic data (n = 103), mRNA microarray data from TCGA (n = 520), METABRIC (n = 1992), and 6 open access breast cancer datasets (n = 1908) were analysed. Patients with Nestin protein expression in tumour cells more often had BRCA1 germline mutations (OR 8.7, p < 0.0005, Series III), especially among younger patients (<40 years at diagnosis) (OR 16.5, p = 0.003). Nestin protein positivity, observed in 9-28% of our hospital cases (Series I-IV), was independently associated with reduced breast cancer specific survival (HR = 2.0, p = 0.035) and was consistently related to basal-like differentiation (by Cytokeratin 5, OR 8.7-13.8, p < 0.0005; P-cadherin OR 7.0-8.9, p < 0.0005; EGFR staining, OR 3.7-8.2, p ≤ 0.05). Nestin mRNA correlated significantly with Nestin protein expression (ρ = 0.6, p < 0.0005), and high levels were seen in the basal-like intrinsic subtype. Gene expression signalling pathways linked to high Nestin were explored, and revealed associations with stem-like tumour features. In summary, Nestin was strongly associated with germline BRCA1 related breast cancer, a basal-like phenotype, reduced survival, and stemness characteristics.
我们在此研究了 Nestin 的蛋白和 mRNA 水平是否可以作为 BRCA1 相关乳腺癌、基底样表型和侵袭性肿瘤的预测因子。我们对独立的乳腺癌医院队列(系列 I-V,共 1257 例)进行了 Nestin 的免疫组织化学染色。此外,还分析了 TCGA 蛋白质组数据(n=103)、TCGA 的 mRNA 微阵列数据(n=520)、METABRIC(n=1992)和 6 个开放获取的乳腺癌数据集(n=1908)。在肿瘤细胞中表达 Nestin 蛋白的患者更常携带 BRCA1 种系突变(OR 8.7,p<0.0005,系列 III),尤其是在较年轻的患者中(诊断时<40 岁)(OR 16.5,p=0.003)。在我们的医院病例中(系列 I-IV)观察到 9-28%的病例存在 Nestin 蛋白阳性,独立与乳腺癌特异性生存降低相关(HR=2.0,p=0.035),并与基底样分化一致相关(通过细胞角蛋白 5,OR 8.7-13.8,p<0.0005;P-钙黏蛋白 OR 7.0-8.9,p<0.0005;EGFR 染色,OR 3.7-8.2,p≤0.05)。Nestin mRNA 与 Nestin 蛋白表达显著相关(ρ=0.6,p<0.0005),并且在基底样内在亚型中可见高水平。探索了与高 Nestin 相关的基因表达信号通路,并发现与肿瘤干细胞特征相关。总之,Nestin 与种系 BRCA1 相关乳腺癌、基底样表型、生存降低和干细胞特征密切相关。