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IGFBP 比值赋予了对 IGF 靶向治疗的抗性,并与乳腺肿瘤侵袭性增加和预后不良相关。

IGFBP ratio confers resistance to IGF targeting and correlates with increased invasion and poor outcome in breast tumors.

机构信息

Department of Oncology, Mayo Clinic, Rochester, MN, USA.

出版信息

Clin Cancer Res. 2012 Mar 15;18(6):1808-17. doi: 10.1158/1078-0432.CCR-11-1806. Epub 2012 Jan 27.

Abstract

PURPOSE

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.

EXPERIMENTAL DESIGN

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.

RESULTS

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.

CONCLUSION

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.

摘要

目的

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。

实验设计

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。

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。

结论

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。

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