Abdollahi Alireza, Jahanian Sepideh, Hemmati Nima, Mohammadpour Hadis
Department of Pathology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Student Research Committee, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Iran J Pathol. 2019 Summer;14(3):223-231. doi: 10.30699/ijp.2019.92094.1894. Epub 2019 Aug 1.
BACKGROUND & OBJECTIVE: Recent studies from gene profiling have revealed some genes that are overexpressed in the epithelial-mesenchymal transition (EMT) process and are responsible for its initiation and activation resulting in tumor progression and metastasis. The present study aimed to assess the role of genes involved in the EMT process and the association of these genes with axillary lymph node and vascular invasion in breast cancer (BC) patients.
In this case-control study, the tumor samples were initially extracted from 33 BC patients. The samples of 15 BC tissues without vascular and axillary invasion were also prepared from the biobank as a control group. RNAs from both tumor and control samples were extracted and stabilized. For assessing overexpression in tumor tissues of selected 18 genes, the real time technique was employed.
There was a significant increase in MMP-2 gene fold expression in tumor cells with vascular invasion regardless of axillary involvement compared to the control group (=0.0008) and also in the comparison of the control group with those with vascular invasion and not axillary lymph node involvement (=0.003). In addition, gene fold expression of tissue inhibitors of metalloproteinase-1(TIMP-1) was decreased in axillary involving tumor cells compared to control group (=0.045), and also in comparison with all samples that did not present any axillary lymph node involvements including the control group and the group with isolated vascular invasion (=0.012).
Overexpression of MMP-2 and under-expression of TIMP-1 were associated with more invasive behavior in breast tumor cells.
近期基因谱研究揭示了一些在上皮-间质转化(EMT)过程中过度表达的基因,这些基因导致EMT过程起始和激活,进而引发肿瘤进展和转移。本研究旨在评估参与EMT过程的基因的作用,以及这些基因与乳腺癌(BC)患者腋窝淋巴结及血管侵犯的相关性。
在这项病例对照研究中,最初从33例BC患者中提取肿瘤样本。还从生物样本库中准备了15例无血管及腋窝侵犯的BC组织样本作为对照组。提取并稳定肿瘤和对照样本的RNA。采用实时技术评估所选18个基因在肿瘤组织中的过表达情况。
与对照组相比(P = 0.0008),无论腋窝受累情况如何,有血管侵犯的肿瘤细胞中MMP-2基因的倍数表达显著增加;与对照组相比,在有血管侵犯但无腋窝淋巴结受累的样本中MMP-2基因的倍数表达也显著增加(P = 0.003)。此外,与对照组相比(P = 0.045),有腋窝受累的肿瘤细胞中金属蛋白酶组织抑制剂-1(TIMP-1)的基因倍数表达降低;与所有无腋窝淋巴结受累的样本(包括对照组和仅有血管侵犯的组)相比(P = 0.012),TIMP-1的基因倍数表达也降低。
MMP-2的过表达和TIMP-1的低表达与乳腺肿瘤细胞更具侵袭性的行为相关。