Expression of collagenases matrix metalloproteinases and YB-1 oncogenic factor in malignant melanoma cancer cells and its regulation by stromal fibroblasts

W. N. Ibrahim, R. A. Wahab, Mohammad Syaiful Bahari Abdull Rasad
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引用次数: 1

Abstract

Background and Objective: Fibroblast stromal cells actively participates in tumor invasion by secreting matrix metalloproteinases (MMPs) within the tumor microenvironment. Expression of these enzymes is primarily regulated at a transcriptional level via interaction with transcription factors. Among these factors, YB-1 oncogenic factor binds with different nucleic acids to exert its diverse influences. Also it represents an important prognostic indicator in many types of tumors. The aim of this study was to assess the expression of collagenases MMPs (MMP1, MMP8, MMP13) and the cellular proliferation in one of the most invasive types of cancer cell types which is the A375 malignant melanoma cancer cell line using co-culture settings. Also, the study attempted to assess the expression of YB-1 factor and its in vivo interaction with the AP-1 gene promoter sequence. Materials and Methods: The experiment involved growing A375 cells with CCD1079SK fibroblasts cells in co-culture environment. The proliferation of cells was determined using serial trypan blue assays, while the expression of YB-1, MMP1, MMP8 and MMP13 was determined by the use of real-time PCR and western blotting analysis. The potential interaction between YB-1 protein and AP-1 promoter sequence was assessed through chromatin immunoprecipitation (ChIP) assay. SPSS with independent t- test was used to compare cell proliferation and real-time PCR Ct mean values between samples. Results: In co-culture setting, the proliferation of A375 cancer cells was significantly faster than the cells in monoculture setting (5.1×105, 3×105 respectively in day 3) (p<0.05). Also, there was a significant increase in the expression of MMP1 enzyme. YB-1 and MMP8 were significantly expressed more in the A375 cancer cells in comparison with normal fibroblasts cells (p<0.05). Conclusion: The study confirms the role of stromal fibroblasts by enhancing the proliferation of melanoma cancer cells in vitro and increasing the expression of the MMP1 enzyme. In addition, YB-1 factor remains as an important prognostic indicator in cancer that might regulate expression of MMPs without binding to the AP-1 promoter sequence.
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胶原酶、基质金属蛋白酶和YB-1癌因子在恶性黑色素瘤癌细胞中的表达及其受间质成纤维细胞的调控
背景与目的:成纤维基质细胞通过在肿瘤微环境中分泌基质金属蛋白酶(MMPs),积极参与肿瘤侵袭。这些酶的表达主要通过与转录因子的相互作用在转录水平上进行调节。其中,YB-1致癌因子与不同的核酸结合,发挥不同的作用。在许多类型的肿瘤中,它也是一个重要的预后指标。本研究的目的是利用共培养环境评估胶原酶MMPs (MMP1、MMP8、MMP13)的表达和A375恶性黑色素瘤细胞系中最具侵袭性的癌细胞类型之一的细胞增殖。此外,本研究试图评估YB-1因子的表达及其与AP-1基因启动子序列的体内相互作用。材料与方法:A375细胞与CCD1079SK成纤维细胞在共培养环境中生长。采用系列台盼蓝法检测细胞增殖,采用实时荧光定量PCR和western blotting检测YB-1、MMP1、MMP8和MMP13的表达。通过染色质免疫沉淀法(ChIP)评估YB-1蛋白与AP-1启动子序列之间潜在的相互作用。采用SPSS软件进行独立t检验,比较不同样本间细胞增殖和实时PCR Ct均值。结果:共培养条件下,A375癌细胞增殖速度明显快于单培养条件下(第3天分别为5.1×105、3×105) (p<0.05)。MMP1酶的表达也显著增加。与正常成纤维细胞相比,YB-1和MMP8在A375癌细胞中的表达明显增加(p<0.05)。结论:间质成纤维细胞在体外促进黑色素瘤癌细胞增殖,增加MMP1酶的表达,证实了间质成纤维细胞的作用。此外,YB-1因子仍然是一个重要的癌症预后指标,它可能在不结合AP-1启动子序列的情况下调节MMPs的表达。
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