Department of Dermatology and Skin Science, Vancouver Coastal Health Research Institute, University of British Columbia, Vancouver, British Columbia, Canada.
Oncogene. 2011 Feb 24;30(8):896-906. doi: 10.1038/onc.2010.470. Epub 2010 Oct 11.
Breast cancer metastasis suppressor 1 (BRMS1) has been reported to suppress metastasis without significantly affecting tumorigenicity in breast cancer and ovarian cancer. To investigate the role of BRMS1 in human melanoma progression and prognosis, we established tissue microarray and BRMS1 expression was evaluated by immunohistochemistry in 41 dysplastic nevi, 90 primary melanomas and 47 melanoma metastases. We found that BRMS1 expression was significantly decreased in metastatic melanoma compared with primary melanoma or dysplastic nevi (P=0.021 and 0.001, respectively, χ(2) test). In addition, reduced BRMS1 staining was significantly correlated with American Joint Committee on Cancer stages (P=0.011, χ(2) test), but not associated with tumor thickness, tumor ulceration and other clinicopathological parameters. Furthermore, BRMS1 expression was significantly correlated with disease-specific 5-year survival of melanoma patients (P=0.007, log-rank test). Multivariate Cox regression analysis revealed that BRMS1 staining was an independent prognostic factor for melanoma patients (relative risk=0.51; confidence interval=0.29-0.91; P=0.022). Moreover, we demonstrated that BRMS1 overexpression inhibited endothelial cell growth and tube formation ability by suppressing NF-κB activity and IL-6 expression in vitro. We also showed that knockdown of BRMS1 increased IL-6 expression and promoted endothelial cell growth and tube formation. In addition, our data revealed that the BRMS1-mediated IL-6 expression is dependent on NF-κB. Strikingly, our in vivo studies using nude mice confirmed that BRMS1 inhibited blood vessel formation and the recruitment of CD31-positive cells in matrigel plugs. Taken together, BRMS1 expression was decreased in metastatic melanomas, which resulted in deficient suppression of angiogenesis and contributed to melanoma progression. BRMS1 may serve an important prognostic marker and therapeutic target for melanoma patients.
乳腺癌转移抑制因子 1(BRMS1)已被报道在乳腺癌和卵巢癌中抑制转移而不显著影响肿瘤发生。为了研究 BRMS1 在人黑色素瘤进展和预后中的作用,我们建立了组织微阵列,并通过免疫组织化学法在 41 个发育不良痣、90 个原发性黑色素瘤和 47 个黑色素瘤转移灶中评估了 BRMS1 的表达。我们发现,与原发性黑色素瘤或发育不良痣相比,转移性黑色素瘤中 BRMS1 的表达显著降低(P=0.021 和 0.001,卡方检验)。此外,BRMS1 染色的减少与美国癌症联合委员会分期显著相关(P=0.011,卡方检验),但与肿瘤厚度、肿瘤溃疡和其他临床病理参数无关。此外,BRMS1 的表达与黑色素瘤患者的疾病特异性 5 年生存率显著相关(P=0.007,对数秩检验)。多变量 Cox 回归分析显示,BRMS1 染色是黑色素瘤患者的独立预后因素(相对风险=0.51;置信区间=0.29-0.91;P=0.022)。此外,我们证明 BRMS1 通过抑制 NF-κB 活性和 IL-6 表达,体外抑制内皮细胞生长和管形成能力。我们还表明,BRMS1 敲低增加了 IL-6 的表达,并促进了内皮细胞的生长和管形成。此外,我们的数据表明,BRMS1 介导的 IL-6 表达依赖于 NF-κB。引人注目的是,我们使用裸鼠进行的体内研究证实,BRMS1 抑制了血管形成和基质胶塞中 CD31 阳性细胞的募集。总之,转移性黑色素瘤中 BRMS1 的表达降低,导致血管生成抑制不足,促进了黑色素瘤的进展。BRMS1 可能成为黑色素瘤患者重要的预后标志物和治疗靶点。