Petrovic Nina, Sami Ahmad, Martinovic Jelena, Zaric Marina, Nakashidze Irina, Lukic Silvana, Jovanovic-Cupic Snezana
University of Belgrade-Vinca, Institute of Nuclear Sciences, Mike Petrovica Alasa 12-14, 11001, Belgrade, Serbia; Institute for Oncology and Radiology of Serbia, Pasterova 14, 11000, Belgrade, Serbia.
University of Belgrade-Vinca, Institute of Nuclear Sciences, Mike Petrovica Alasa 12-14, 11001, Belgrade, Serbia.
Pathol Res Pract. 2017 Oct;213(10):1264-1270. doi: 10.1016/j.prp.2017.08.012. Epub 2017 Sep 6.
Breast carcinomas (BC) belong to a heterogeneous group of malignant diseases. Correct categorization of BC based on molecular biomarkers has a very important role in deciding the proper course of therapy for each patient. It has been already shown that the decrease of TIMP metalloproteinase inhibitor 3 (TIMP-3) together with overexpression of microRNA-21 (miR-21) might be involved in the process of BC invasion. This is the first study that examined relationship among miR-21, TIMP-3 mRNA and TIPM-3 protein levels in BC groups formed according to invasiveness.
In this study, we used 46 breast cancer samples. Estrogen and progesterone receptor (ER, PR) protein levels were evaluated by immunohistochemistry (IHC) method. TIMP-3 mRNA expression was examined by two-step real-time quantitative PCR (qRT-PCR). Western blot analysis was performed for 16 samples.
Statistically significant differences in TIMP-3 expression levels between invasive groups were discovered in ER positive (ER+) (p=0.015), Her-2 negative (p=0.026) subgroups, and patients without lymph-node metastasis (p=0.039). Interestingly, significant positive correlation was detected between miR-21 and TIMP-3 mRNA levels (P<0.001, ρ=0.949) in the group of in situ tumors. TIMP-3 mRNA expression levels highly negatively correlated with levels of miR-21 in PR+ invasive BCs (p=0.007, ρ=-0.641). TIMP-3 protein levels negatively correlated with miR-21 levels in pure invasive BCs.
These data suggest that signaling pathways involved in formation and progression of BCs in groups formed according to invasiveness might be different. Our findings propose that TIMP-3 mRNA expression levels could be significant prognostic parameter, but within specific BC subtypes.
乳腺癌(BC)属于一组异质性恶性疾病。基于分子生物标志物对BC进行正确分类对于确定每位患者的适当治疗方案具有非常重要的作用。已经表明,金属蛋白酶组织抑制剂3(TIMP-3)的减少以及微小RNA-21(miR-21)的过表达可能参与BC侵袭过程。这是第一项研究根据侵袭性形成的BC组中miR-21、TIMP-3 mRNA和TIMP-3蛋白水平之间的关系。
在本研究中,我们使用了46个乳腺癌样本。通过免疫组织化学(IHC)方法评估雌激素和孕激素受体(ER、PR)蛋白水平。通过两步实时定量PCR(qRT-PCR)检测TIMP-3 mRNA表达。对16个样本进行蛋白质印迹分析。
在雌激素受体阳性(ER+)(p=0.015)、人表皮生长因子受体2阴性(p=0.026)亚组以及无淋巴结转移的患者(p=0.039)中,侵袭性组之间TIMP-3表达水平存在统计学显著差异。有趣的是,在原位肿瘤组中,miR-21与TIMP-3 mRNA水平之间检测到显著正相关(P<0.001,ρ=0.949)。在PR+侵袭性BC中,TIMP-3 mRNA表达水平与miR-21水平高度负相关(p=0.007,ρ=-0.641)。在纯侵袭性BC中,TIMP-3蛋白水平与miR-21水平负相关。
这些数据表明,根据侵袭性形成的BC组中参与BC形成和进展的信号通路可能不同。我们的研究结果表明,TIMP-3 mRNA表达水平可能是一个重要的预后参数,但仅限于特定的BC亚型。