Division of Oncology, Department of Clinical Sciences, Lund, Lund University and Skåne University Hospital, Barngatan 4, SE 221 85 Lund, Sweden.
Department of Hematology, Oncology and Radiation Physics, Skåne University Hospital, Lund, Sweden.
Carcinogenesis. 2021 Nov 12;42(11):1314-1325. doi: 10.1093/carcin/bgab090.
The prognostic impact of insulin-like growth factor binding protein 7 (IGFBP7) in breast cancer is unclear. Host factors, including lifestyle, anthropometry and metabolic profile, might influence tumor-specific IGFBP7. This study aimed to investigate whether IGFBP7 levels and messenger ribonucleic acid (mRNA) expression are associated with the patient and tumor characteristics and prognosis in breast cancer. Patients with primary breast cancer in Lund, Sweden, were included preoperatively in the study between 2002 and 2012 (n = 1018). Tumor-specific IGFBP7 protein levels were evaluated with immunohistochemistry using tissue microarrays in tumors from 878 patients. IGFBP7 mRNA expression and its corresponding clinical data were obtained from The Cancer Genome Atlas and analyzed for 809 patients. Tumor-specific IGFBP7 protein levels were categorized based on Histo 300 scores into IGFBP7low (6.2%), IGFBP7intermediate (75.7%) and IGFBP7high (18.1%). Both low IGFBP7 protein levels and mRNA expression were associated with less aggressive tumor characteristics. Overall, IGFBP7low conferred low recurrence risk. The prognostic impact of IGFBP7high varied according to any alcohol consumption and tamoxifen treatment. IGFBP7high was associated with low recurrence risk in alcohol consumers but high recurrence risk in alcohol abstainers (Pinteraction= 0.039). Moreover, the combination of IGFBP7high and estrogen receptor-positive tumors was associated with low recurrence risk only in tamoxifen-treated patients (Pinteraction= 0.029). To conclude, IGFBP7low might be a good, independent prognosticator in breast cancer. The prognostic impact of IGFBP7high depends on host factors and treatment. IGFBP7 merits further investigation to confirm whether it could be a suitable biomarker for treatment selection.
胰岛素样生长因子结合蛋白 7(IGFBP7)在乳腺癌中的预后影响尚不清楚。宿主因素,包括生活方式、人体测量学和代谢特征,可能会影响肿瘤特异性 IGFBP7。本研究旨在探讨 IGFBP7 水平和信使核糖核酸(mRNA)表达是否与乳腺癌患者和肿瘤特征及预后相关。2002 年至 2012 年间,在瑞典隆德的原发性乳腺癌患者在术前被纳入研究(n = 1018)。使用组织微阵列免疫组织化学法评估了 878 例患者肿瘤中的肿瘤特异性 IGFBP7 蛋白水平。从癌症基因组图谱获得 IGFBP7 mRNA 表达及其相应的临床数据,并对 809 例患者进行了分析。基于 Histo 300 评分,肿瘤特异性 IGFBP7 蛋白水平分为 IGFBP7 低(6.2%)、IGFBP7 中(75.7%)和 IGFBP7 高(18.1%)。低 IGFBP7 蛋白水平和 mRNA 表达均与侵袭性较弱的肿瘤特征相关。总体而言,IGFBP7 低预示着复发风险低。IGFBP7 高的预后影响取决于是否饮酒和是否服用他莫昔芬。在饮酒者中,IGFBP7 高与低复发风险相关,但在不饮酒者中,IGFBP7 高与高复发风险相关(P 交互=0.039)。此外,IGFBP7 高和雌激素受体阳性肿瘤的组合仅在服用他莫昔芬的患者中与低复发风险相关(P 交互=0.029)。总之,IGFBP7 低可能是乳腺癌的良好独立预后标志物。IGFBP7 高的预后影响取决于宿主因素和治疗。需要进一步研究 IGFBP7,以确认其是否可以作为治疗选择的合适生物标志物。