Breast Biology Group, Institute of Cancer Sciences, Paterson Institute for Cancer Research, University of Manchester, Manchester, United Kingdom.
Clin Cancer Res. 2013 Feb 1;19(3):643-56. doi: 10.1158/1078-0432.CCR-12-1063. Epub 2012 Nov 13.
Breast cancer stem-like cells (CSC) are an important therapeutic target as they are predicted to be responsible for tumor initiation, maintenance, and metastases. Interleukin (IL)-8 is upregulated in breast cancer and is associated with poor prognosis. Breast cancer cell line studies indicate that IL-8 via its cognate receptors, CXCR1 and CXCR2, is important in regulating breast CSC activity. We investigated the role of IL-8 in the regulation of CSC activity using patient-derived breast cancers and determined the potential benefit of combining CXCR1/2 inhibition with HER2-targeted therapy.
CSC activity of metastatic and invasive human breast cancers (n = 19) was assessed ex vivo using the mammosphere colony-forming assay.
Metastatic fluid IL-8 level correlated directly with mammosphere formation (r = 0.652; P < 0.05; n = 10). Recombinant IL-8 directly increased mammosphere formation/self-renewal in metastatic and invasive breast cancers (n = 17). IL-8 induced activation of EGFR/HER2 and downstream signaling pathways and effects were abrogated by inhibition of SRC, EGFR/HER2, phosphoinositide 3-kinase (PI3K), or MEK. Furthermore, lapatinib, which targets EGFR/HER2, inhibited the mammosphere-promoting effect of IL-8 in both HER2-positive and negative patient-derived cancers. CXCR1/2 inhibition also blocked the effect of IL-8 on mammosphere formation and added to the efficacy of lapatinib in HER2-positive cancers.
These studies establish a role for IL-8 in the regulation of patient-derived breast CSC activity and show that IL-8/CXCR1/2 signaling is partly mediated via a novel SRC and EGFR/HER2-dependent pathway. Combining CXCR1/2 inhibitors with current HER2-targeted therapies has potential as an effective therapeutic strategy to reduce CSC activity in breast cancer and improve the survival of HER2-positive patients.
乳腺癌干细胞样细胞(CSC)是一个重要的治疗靶点,因为它们被预测负责肿瘤的起始、维持和转移。白细胞介素(IL)-8 在乳腺癌中上调,并与预后不良相关。乳腺癌细胞系研究表明,IL-8 通过其同源受体 CXCR1 和 CXCR2,在调节乳腺癌 CSC 活性方面起着重要作用。我们使用患者来源的乳腺癌研究了 IL-8 在调节 CSC 活性中的作用,并确定了联合 CXCR1/2 抑制与 HER2 靶向治疗的潜在益处。
使用乳腺球体集落形成测定法,在体外评估转移性和侵袭性人乳腺癌(n = 19)的 CSC 活性。
转移性液体中 IL-8 水平与乳腺球体形成直接相关(r = 0.652;P < 0.05;n = 10)。重组 IL-8 直接增加转移性和侵袭性乳腺癌的乳腺球体形成/自我更新(n = 17)。IL-8 诱导 EGFR/HER2 和下游信号通路的激活,这些作用可通过抑制 SRC、EGFR/HER2、磷酸肌醇 3-激酶(PI3K)或 MEK 来阻断。此外,针对 EGFR/HER2 的拉帕替尼抑制了 IL-8 在 HER2 阳性和阴性患者来源的癌症中促进乳腺球体形成的作用。CXCR1/2 抑制也阻断了 IL-8 对乳腺球体形成的作用,并增加了拉帕替尼在 HER2 阳性癌症中的疗效。
这些研究确立了 IL-8 在调节患者来源的乳腺癌 CSC 活性中的作用,并表明 IL-8/CXCR1/2 信号部分通过一种新的 SRC 和 EGFR/HER2 依赖性途径介导。将 CXCR1/2 抑制剂与目前的 HER2 靶向治疗联合使用,作为一种减少乳腺癌 CSC 活性并提高 HER2 阳性患者生存率的有效治疗策略具有潜力。