Fernández Cecilia A, Yan Li, Louis Gwendolyn, Yang Jiang, Kutok Jeffery L, Moses Marsha A
Vascular Biology Program and Department of Surgery, Children's Hospital Boston, MA, USA.
Clin Cancer Res. 2005 Aug 1;11(15):5390-5. doi: 10.1158/1078-0432.CCR-04-2391.
Having previously shown that the binding of neutrophil gelatinase-associated lipocalin (NGAL) to matrix metalloproteinase-9 (MMP-9) protects this extracellular matrix remodeling enzyme from autodegradation, we hypothesized that the addition of NGAL to breast cancer cells, which do not express this protein but do express MMP-9, might result in a more aggressive phenotype in vivo. Based on our previous reports that MMPs can be detected in the urine of cancer patients, we also asked whether MMP-9/NGAL could be detected in the urine of breast cancer patients and whether it might be predictive of disease status.
Clones of MCF-7 human breast cancer cells differentially expressing NGAL were generated by stable transfection with human NGAL expression constructs. The established clones were then implanted s.c. in immunodeficient mice and tumor growth was monitored. In addition, we analyzed the urine of individuals with breast cancer and age-matched, sex-matched controls using gelatin zymography for the presence of MMP-9/NGAL.
Increased NGAL expression resulted in significant stimulation of tumor growth. Immunohistochemical analysis of MCF-7 tumors revealed that the NGAL-overexpressing ones exhibited increased growth rates that were accompanied by increased levels of MMP-9, increased angiogenesis, and an increase in the tumor cell proliferative fraction. In addition, MMP-9/NGAL complex was detected in 86.36% of the urine samples from breast cancer patients but not in those from healthy age and sex-matched controls.
These findings suggest, for the first time, that NGAL may play an important role in breast cancer in vivo by protecting MMP-9 from degradation thereby enhancing its enzymatic activity and facilitating angiogenesis and tumor growth. Clinically, these data suggest that the urinary detection of MMP-9/NGAL may be useful in noninvasively predicting disease status of breast cancer patients.
先前研究表明,中性粒细胞明胶酶相关脂质运载蛋白(NGAL)与基质金属蛋白酶-9(MMP-9)结合可保护这种细胞外基质重塑酶免于自降解,我们据此推测,向不表达该蛋白但表达MMP-9的乳腺癌细胞中添加NGAL可能会在体内导致更具侵袭性的表型。基于我们之前关于基质金属蛋白酶可在癌症患者尿液中检测到的报道,我们还询问了乳腺癌患者尿液中是否能检测到MMP-9/NGAL,以及它是否可预测疾病状态。
通过用人类NGAL表达构建体进行稳定转染,生成差异表达NGAL的MCF-7人乳腺癌细胞克隆。然后将建立的克隆皮下植入免疫缺陷小鼠体内,并监测肿瘤生长。此外,我们使用明胶酶谱法分析乳腺癌患者及年龄匹配、性别匹配的对照个体的尿液中是否存在MMP-9/NGAL。
NGAL表达增加导致肿瘤生长显著受刺激。对MCF-7肿瘤的免疫组织化学分析显示,过表达NGAL的肿瘤生长速率增加,同时伴有MMP-9水平升高、血管生成增加以及肿瘤细胞增殖分数增加。此外,在86.36%的乳腺癌患者尿液样本中检测到MMP-9/NGAL复合物,而在年龄和性别匹配的健康对照者尿液中未检测到。
这些发现首次表明,NGAL可能通过保护MMP-9免于降解,从而增强其酶活性并促进血管生成和肿瘤生长,在乳腺癌体内发挥重要作用。临床上,这些数据表明尿液中MMP-9/NGAL的检测可能有助于无创预测乳腺癌患者的疾病状态。