Ławicki Paweł, Malinowski Paweł, Motyka Joanna, Ławicki Michał, Kicman Aleksandra, Kulesza Monika, Gacuta Ewa, Guszczyn Tomasz, Januszkiewicz Marcin, Zbucka-Krętowska Monika, Ławicki Sławomir
Department of Population Medicine and Lifestyle Diseases Prevention, Medical University of Bialystok, 15-269 Bialystok, Poland.
Department of Oncological Surgery, Bialystok Oncology Center, 15-276 Bialystok, Poland.
J Clin Med. 2023 Mar 30;12(7):2618. doi: 10.3390/jcm12072618.
Matrix metalloproteinases (MMPs) are a group of enzymes that mediate both physiological and pathological processes such as carcinogenesis. The role of matrix metalloproteinase-3 (MMP-3) and (MMP-7) in the pathogenesis of breast cancer (BC) has been demonstrated, suggesting that they may be considered as potential markers of this condition. The aim of this study was to assess plasma concentrations and diagnostic utility of MMP-3 and MMP-7 in 100 patients with early-stage breast cancer with Luminal A subtype or Luminal B HER-negative subtype, before and after surgical treatment, and in the following control groups: patients with a benign tumor () and healthy subjects. The concentrations of MMP-3 and MMP-7 were referenced to the levels of the widely recognized marker for BC diagnosis CA 15-3. MMP-3 and MMP-7 was measured by ELISA method and CA 15-3 by CMIA. Plasma levels of MMP-7 were significantly higher in Luminal A and Luminal B HER2-negative subtype breast cancer patients as compared to the healthy group. MMP-7 demonstrated comparable but mostly higher to CA 15-3 or MMP-3 values of diagnostic sensitivity, specificity, positive and negative predictive values and AUC (0.6888 for Luminal A subtype; 0.7612 for Luminal B HER2-negative; 0.7250 for BC total group, respectively) in the groups tested. The combined use of the tested parameters resulted in a further increase in diagnostic criteria and AUC. These results suggest the usefulness of combining MMP-7 with CA 15-3 in the diagnostics of breast cancer, especially in Luminal B HER2-negative subtypes patients, as a new candidate for tumor markers.
基质金属蛋白酶(MMPs)是一类介导诸如致癌作用等生理和病理过程的酶。基质金属蛋白酶-3(MMP-3)和(MMP-7)在乳腺癌(BC)发病机制中的作用已得到证实,这表明它们可被视为该疾病的潜在标志物。本研究的目的是评估100例Luminal A亚型或Luminal B HER阴性亚型早期乳腺癌患者在手术治疗前后血浆中MMP-3和MMP-7的浓度及诊断效用,并与以下对照组进行比较:良性肿瘤患者()和健康受试者。MMP-3和MMP-7的浓度以广泛认可的BC诊断标志物CA 15-3的水平为参照。采用酶联免疫吸附测定(ELISA)法检测MMP-3和MMP-7,采用化学发光微粒子免疫分析(CMIA)法检测CA 15-3。与健康组相比,Luminal A和Luminal B HER2阴性亚型乳腺癌患者血浆中MMP-7水平显著更高。在测试组中,MMP-7的诊断敏感性、特异性、阳性和阴性预测值以及曲线下面积(AUC)与CA 15-3或MMP-3的值相当,但大多更高(Luminal A亚型为0.6888;Luminal B HER2阴性为0.7612;BC总组为0.7250)。联合使用所检测的参数导致诊断标准和AUC进一步提高。这些结果表明,将MMP-7与CA 15-3联合用于乳腺癌诊断具有实用性,尤其是在Luminal B HER2阴性亚型患者中,可作为肿瘤标志物的新候选物。