Azadeh Jouneghani Mehrnoush, Keshavarzi Fatemeh, Haghnazari Nahid, Hooshmandi Zahra, Amini Sabrieh
Department of Biology, Sanandaj Branch, Islamic Azad University, Sanandaj, Iran.
Clin Med Insights Oncol. 2023 Nov 3;17:11795549231207835. doi: 10.1177/11795549231207835. eCollection 2023.
B-cell leukemia/lymphoma 2 ( gene regulates carcinogenesis by inhibiting apoptosis. This study evaluated the association of 3'-untranslated regions (3' UTR) rs1564483 polymorphism and miR-296-3p with the development of breast and gastric cancers.
A microarray analysis was performed on the Genomic Spatial Event (GSE)29431 and GSE161533 datasets for breast and gastric cancers. Blood samples were taken from 222 (111 patients and 111 controls) and 210 (84 patients and 126 controls) individuals for breast and gastric cancers, respectively. Genomic DNA was extracted from the blood samples and genotyping was performed using real-time polymerase chain reaction (RT-PCR), followed by examining the high-temperature melting curve. Statistical analysis was conducted to examine the potential correlation between the rs1564483 polymorphism and the risk of breast and gastric cancers concerning pathological characteristics.
The results of the microarray showed that the gene was up-regulated in gastric cancer (logFC [log fold change]: 0.65, adjusted < .05). Clinical outcome showed no notable relationship between the rs1564483 polymorphism and breast cancer risk; however, for gastric cancer, it identified a large difference between healthy controls and patients for an allelic frequency of rs1564483 ( ⩽ .001). Moreover, an assay of different models (dominant, recessive, and co-dominant) showed a significant association between the AG genotype between control and gastric cases (Pearson chi-square test, = .046). In addition, the prevalence of the AG genotype was greater in persons under the age of 45 and in patients with infection ( ⩽ .001). The AG genotype was not related to smoking, although the AA genotype was associated with increased cancer incidence in smokers ( ⩽ .001).
In silico studies and calculations of the ΔG binding of micro ribonucleic acid (miRNA) hsa-miR-296-3p to the mutant and wild alleles of the rs15644833 single nucleotide polymorphism (SNP) have revealed that Bcl-2 mRNA expression in gastric cancer decreases, thus confirming the tumor suppressor role of the gene.
B细胞淋巴瘤/白血病-2(Bcl-2)基因通过抑制细胞凋亡来调控肿瘤发生。本研究评估了3'-非翻译区(3'UTR)rs1564483多态性及miR-296-3p与乳腺癌和胃癌发生发展的关联。
对乳腺癌和胃癌的基因组空间事件(GSE)29431和GSE161533数据集进行微阵列分析。分别从222名个体(111例患者和111例对照)和210名个体(84例患者和126例对照)采集乳腺癌和胃癌的血样。从血样中提取基因组DNA,采用实时聚合酶链反应(RT-PCR)进行基因分型,随后检测高温熔解曲线。进行统计学分析以检验rs1564483多态性与乳腺癌和胃癌风险及病理特征之间的潜在相关性。
微阵列分析结果显示,Bcl-2基因在胃癌中上调(logFC[对数倍变化]:0.65,校正后P<0.05)。临床结果显示,rs1564483多态性与乳腺癌风险之间无显著关联;然而,对于胃癌,rs1564483的等位基因频率在健康对照与患者之间存在显著差异(P≤0.001)。此外,不同模型(显性、隐性和共显性)分析显示,对照与胃癌病例之间AG基因型存在显著关联(Pearson卡方检验,P = 0.046)。此外,AG基因型在45岁以下人群及幽门螺杆菌感染患者中更为常见(P≤0.001)。AG基因型与吸烟无关,尽管AA基因型与吸烟者癌症发病率增加有关(P≤0.001)。
对微小核糖核酸(miRNA)hsa-miR-296-3p与rs1564483单核苷酸多态性(SNP)突变和野生等位基因结合的ΔG进行的计算机模拟研究和计算表明,胃癌中Bcl-2 mRNA表达降低,从而证实了Bcl-2基因的肿瘤抑制作用。