Saleem Mohammed A, Mustafa Mustafa S
Department of Biology, College of Science, Salahaddin University-Erbil, Erbil, IRQ.
Cureus. 2024 Aug 8;16(8):e66467. doi: 10.7759/cureus.66467. eCollection 2024 Aug.
Prostate cancer (PCa) is recognized as one of the most common malignancies that greatly affects the male population globally. Breast cancer gene 1 () is an important tumor suppressor gene that plays a central role in the maintenance of genomic integrity by promoting the repair of double-strand breaks of DNA. Here, we present a pilot study to examine the promoter methylation and gene expression of the gene in patients with PCa in Erbil governorate, Iraq. The collection of samples took place in Erbil City, Iraq, specifically at Rizgary Hospital, PAR Hospital, and Al-Mufti's private laboratory. A total of 40 tissue samples were collected from age-matched individuals, comprising 30 pathologically confirmed PCa cases and 10 normal prostatic tissue taken from individuals who, during diagnosis, were found to be negative for PCa. Data on demographic and clinical information, such as pathological stage, age, and prostate-specific antigen (PSA) level, were gathered from the medical records. The impact of the promoter methylation was forecasted using the DNA bisulfite conversion technique and methyl-specific PCR (MSP) with specific primers for the promoter region. The assessment of expression was conducted using quantitative real-time PCR (qPCR). Among the 30 patients examined, 76.6% (23 cases) were found to have promoter methylation, and none of the normal tissues appeared to have DNA methylation. promoter methylation was positively associated with the advanced stage of disease (p=0.01) and Gleason score (p=0.007). The analysis revealed a significant downregulation of the gene expression in methylated tumor samples as compared to non-methylated tumors and normal tissues, suggesting the role of epigenetic silencing. To the best of our knowledge, this is the first study investigating methylation status and level of mRNA transcripts among PCa patients in Iraq. Our findings suggest that promoter hypermethylation of the gene could serve as a viable biomarker for PCa, marking a significant discovery.
前列腺癌(PCa)被认为是全球范围内对男性群体影响极大的最常见恶性肿瘤之一。乳腺癌基因1( )是一种重要的肿瘤抑制基因,通过促进DNA双链断裂的修复在维持基因组完整性方面发挥核心作用。在此,我们开展了一项初步研究,以检测伊拉克埃尔比勒省PCa患者中该基因的启动子甲基化和基因表达情况。样本采集在伊拉克埃尔比勒市进行,具体是在里兹加里医院、PAR医院和穆夫提私人实验室。总共从年龄匹配的个体中收集了40份组织样本,其中包括30例经病理确诊的PCa病例以及10份取自诊断时PCa呈阴性个体的正常前列腺组织。从病历中收集了人口统计学和临床信息数据,如病理分期、年龄和前列腺特异性抗原(PSA)水平。使用DNA亚硫酸氢盐转化技术和针对该基因启动子区域的特异性引物进行甲基化特异性PCR(MSP)来预测启动子甲基化的影响。使用定量实时PCR(qPCR)进行该基因表达的评估。在所检测的30例患者中,发现76.6%(23例)存在该基因启动子甲基化,而正常组织均未出现DNA甲基化。该基因启动子甲基化与疾病晚期(p = 0.01)和 Gleason评分(p = 0.007)呈正相关。分析显示,与未甲基化肿瘤和正常组织相比,甲基化肿瘤样本中该基因表达显著下调,提示表观遗传沉默的作用。据我们所知,这是第一项调查伊拉克PCa患者中该基因甲基化状态和mRNA转录水平的研究。我们的研究结果表明,该基因启动子高甲基化可作为PCa的一种可行生物标志物,这是一项重大发现。