Department of Oncology, Mayo Clinic, Rochester, MN, USA.
Clin Cancer Res. 2012 Mar 15;18(6):1808-17. doi: 10.1158/1078-0432.CCR-11-1806. Epub 2012 Jan 27.
To improve the significance of insulin-like growth factor-binding protein 5 (IGFBP-5) as a prognostic and potentially predictive marker in patients with breast cancer.
Increased IGFBP-5 expression was identified in MCF-7 cells resistant (MCF-7R4) to the IGF-1R/insulin receptor (InsR) inhibitor BMS-536924 and its role examined by targeted knockdown and overexpression in multiple experimental models. Protein expression of IGFBP-5 was measured by immunohistochemistry in a cohort of 76 patients with breast cancer to examine correlative associations with invasive tumor fraction and outcome. The use of a combined IGFBP-5/IGFBP-4 (BPR) expression ratio was applied to predict anti-IGF-1R/InsR response in a panel of breast cancer lines and outcome in multiple breast tumor cohorts.
IGFBP-5 knockdown decreased BMS-536924 resistance in MCF-7R4 cells, whereas IGFBP-5 overexpression in MCF-7 cells conferred resistance. When compared with pathologically normal reduction mammoplasty tissue, IGFBP-5 expression levels were upregulated in both invasive and histologically normal adjacent breast cancer tissue. In both univariate and multivariate modeling, metastasis-free survival, recurrence free survival (RFS), and overall survival (OS) were significantly associated with high IGFBP-5 expression. Prognostic power of IGFBP-5 was further increased with the addition of IGFBP-4 where tumors were ranked based upon IGFBP-5/IGFBP-4 expression ratio (BPR). Multiple breast cancer cohorts confirm that BPR (high vs. low) was a strong predictor of RFS and OS.
IGFBP-5 expression is a marker of poor outcome in patients with breast cancer. An IGFBP-5/IGFBP-4 expression ratio may serve as a surrogate biomarker of IGF pathway activation and predict sensitivity to anti-IGF-1R targeting.
提高胰岛素样生长因子结合蛋白 5(IGFBP-5)作为乳腺癌患者预后和潜在预测标志物的意义。
在对 IGF-1R/胰岛素受体(InsR)抑制剂 BMS-536924 耐药的 MCF-7 细胞(MCF-7R4)中鉴定出 IGFBP-5 表达增加,并在多个实验模型中通过靶向敲低和过表达来研究其作用。在 76 例乳腺癌患者的队列中,通过免疫组织化学法测量 IGFBP-5 的蛋白表达,以检查与浸润性肿瘤分数和结果的相关性。联合使用 IGFBP-5/IGFBP-4(BPR)表达比值,用于预测一系列乳腺癌细胞系对 IGF-1R/InsR 抑制剂的反应和多个乳腺癌肿瘤队列的结果。
IGFBP-5 敲低降低了 MCF-7R4 细胞对 BMS-536924 的耐药性,而在 MCF-7 细胞中过表达 IGFBP-5 则赋予了耐药性。与病理性正常的乳腺缩小成形术组织相比,侵袭性和组织学正常的乳腺癌相邻组织中 IGFBP-5 的表达水平均上调。在单因素和多因素建模中,无转移生存、无复发生存(RFS)和总生存(OS)与高 IGFBP-5 表达显著相关。当加入 IGFBP-4 时,IGFBP-5 的预后能力进一步提高,其中根据 IGFBP-5/IGFBP-4 表达比值(BPR)对肿瘤进行分级。多个乳腺癌队列证实,BPR(高 vs. 低)是 RFS 和 OS 的强有力预测因子。
IGFBP-5 的表达是乳腺癌患者预后不良的标志物。IGFBP-5/IGFBP-4 表达比值可作为 IGF 通路激活的替代生物标志物,并预测对 IGF-1R 靶向治疗的敏感性。