University of Michigan Comprehensive Cancer Center, Department of Internal Medicine/Oncology, Ann Arbor, Michigan 48109-0015, USA.
J Clin Invest. 2010 Feb;120(2):485-97. doi: 10.1172/JCI39397. Epub 2010 Jan 4.
Recent evidence suggests that breast cancer and other solid tumors possess a rare population of cells capable of extensive self-renewal that contribute to metastasis and treatment resistance. We report here the development of a strategy to target these breast cancer stem cells (CSCs) through blockade of the IL-8 receptor CXCR1. CXCR1 blockade using either a CXCR1-specific blocking antibody or repertaxin, a small-molecule CXCR1 inhibitor, selectively depleted the CSC population in 2 human breast cancer cell lines in vitro. Furthermore, this was followed by the induction of massive apoptosis in the bulk tumor population via FASL/FAS signaling. The effects of CXCR1 blockade on CSC viability and on FASL production were mediated by the FAK/AKT/FOXO3A pathway. In addition, repertaxin was able to specifically target the CSC population in human breast cancer xenografts, retarding tumor growth and reducing metastasis. Our data therefore suggest that CXCR1 blockade may provide a novel means of targeting and eliminating breast CSCs.
最近的证据表明,乳腺癌和其他实体瘤具有一种罕见的细胞群体,能够进行广泛的自我更新,从而导致转移和治疗耐药。我们在这里报告了一种通过阻断白细胞介素-8 受体 CXCR1 来靶向这些乳腺癌干细胞 (CSC) 的策略。使用 CXCR1 特异性阻断抗体或小分子 CXCR1 抑制剂 repertaxin 阻断 CXCR1,可选择性地耗尽体外 2 个人乳腺癌细胞系中的 CSC 群体。此外,这会通过 FASL/FAS 信号诱导大量肿瘤细胞群体的凋亡。CXCR1 阻断对 CSC 活力和 FASL 产生的影响是由 FAK/AKT/FOXO3A 途径介导的。此外,repertaxin 能够特异性地靶向人乳腺癌异种移植中的 CSC 群体,从而减缓肿瘤生长和减少转移。因此,我们的数据表明,CXCR1 阻断可能为靶向和消除乳腺癌 CSC 提供一种新方法。