Alterations of glutathione and GSTM1 mutations induce tumor metastasis and invasion via EMT pathway in breast cancer patients

Arshad Ali, Ayaz Ali, Shafiq Ahmad
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Abstract

Purpose: Alteration in the Glutathione (GSH) and Glutathione S-Transferase (GST) family lead to various disorders including breast cancer. However, the role of GSH and GSTM1 in the onset of breast cancer is still not fully elucidated. Objective: In the present study we observed considerable deficiency in the levels of glutathione and genetic mutation in the GSTM1 enzyme that influence susceptibility to breast cancer metastasis and invasion via EMT pathway. Methods: GSTM1 genotype was identified by multiplex polymerase chain reaction (PCR), RT-PCR and western blotting in breast cancer tissue samples and ANCT samples. The endogenous glutathione levels were determined by HPLC. The tumor metastasis, invasion and EMT biomarkers were determined by RT-PCR and western blot. The relationship between breast cancer, disease progression and histological status were estimated by one way analysis of variance and descriptive statistic. Data were analyzed using OriginPro 2015 statistics software (OriginLab, Northampton, USA). The correlation among different factors was assessed at 95% confidence intervals (CI) using the Mann-Whitney, Kruskal Wallis, and ANOVA test. P<0.05 was considered significant. Results: In present study genotyping analysis of GST investigated that genetic mutation in GSTM1 was detected in breast cancer tissue samples. Moreover, messenger RNA and protein analysis showed that GSTM1 was significant downregulated in tumor tissues (p=0.005, p=0.02) of breast cancer patients. Furthermore, significant reduction in the level of total glutathione level (GSHt P<0.05) was observed among correlation with patient ages, stages and histological grades, of breast cancer patients. Additionally, the result revealed that downregulation of GSTM1 promotes EMT pathway that leads to enhanced the expression of tumor proliferation, invasion and metastasis in breast cancer tissue samples compared with the ANCT samples (P<0.05). Conclusions The present findings suggest that GSTM1 genotype could be a potential biomarker that regulate EMT pathway associated with breast cancer prognosis.
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谷胱甘肽和GSTM1突变的改变可通过EMT途径诱导乳腺癌患者的肿瘤转移和侵袭
目的:谷胱甘肽(GSH)和谷胱甘肽s -转移酶(GST)家族的改变导致包括乳腺癌在内的各种疾病。然而,GSH和GSTM1在乳腺癌发病中的作用仍未完全阐明。目的:在本研究中,我们观察到谷胱甘肽水平的显著缺乏和GSTM1酶的基因突变影响乳腺癌通过EMT途径转移和侵袭的易感性。方法:采用多重聚合酶链反应(PCR)、RT-PCR和western blotting对乳腺癌组织样本和ANCT样本进行GSTM1基因型鉴定。采用高效液相色谱法测定内源性谷胱甘肽水平。采用RT-PCR和western blot检测肿瘤转移、侵袭和EMT生物标志物。采用单因素方差分析和描述性统计方法对乳腺癌、疾病进展和组织学状态之间的关系进行估计。使用OriginPro 2015统计软件(OriginLab, Northampton, USA)对数据进行分析。使用Mann-Whitney、Kruskal Wallis和ANOVA检验,以95%置信区间(CI)评估不同因素之间的相关性。P<0.05为差异有统计学意义。结果:本研究通过GST基因分型分析,在乳腺癌组织样本中检测到GSTM1基因突变。此外,信使RNA和蛋白分析显示,GSTM1在乳腺癌患者的肿瘤组织中显著下调(p=0.005, p=0.02)。总谷胱甘肽水平与乳腺癌患者年龄、分期、组织学分级相关,均显著降低(P<0.05)。此外,与ANCT相比,下调GSTM1可促进EMT通路,导致乳腺癌组织样本中肿瘤增殖、侵袭和转移的表达增强(P<0.05)。结论GSTM1基因型可能是调控EMT通路与乳腺癌预后相关的潜在生物标志物。
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