前列腺癌患者外周血中MST1基因表达水平的降低

Fariba Karimian, M. Sahmani, Amirhosein Maali, T. Farivar, A. Karimi, M. Azad
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引用次数: 0

摘要

背景:前列腺癌(PC)是男性第二常见的恶性肿瘤,占所有癌症的12.5%。分子研究(如RNA表达分析)的发展有助于这种癌症的特征,新的治疗靶点的发展,以及新的预后和诊断生物标志物的引入。近年来的研究证实,哺乳动物不育20样激酶(MST1)是一种肿瘤抑制基因,已被引入作为某些特定癌症的生物标志物。在本研究中,由于PC的遗传模式,我们关注的是MST1在PC患者白细胞中的表达水平。方法:本研究分为两组,分别为20例PC患者和20例健康人。提取RNA和合成cDNA后,进行实时荧光定量PCR检测MST1的表达水平。选择GAPDH作为内控基因。采用“Rotor-Gene Q系列软件2.3.1”和“Rest 2.0.13软件”进行统计分析。结果:本研究对20例50 ~ 70岁的PC患者和20例健康人进行了研究,结果显示,PC患者WBC样本中MST1表达水平比正常人低约62% (P<0.01)。结论:引入MST1的低表达水平作为前列腺癌的生物标志物需要补充研究。然而,在本研究中,MST1的生物标志物验证和潜力已经得到认可。
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Reduced Expression Levels of the MST1 gene in the Peripheral Blood of Patients with Prostate Cancer
Background: Prostate cancer (PC) is the second most common malignancy among men, accounting for 12.5% of all cancers. The development of molecular studies (such as RNA expression analysis) aids the characterization of this cancer, the development of new targets for therapy, and the introduction of novel prognostic and diagnostic biomarkers. Recent studies have confirmed Mammalian Sterile 20-Like kinase (MST1) as a tumor suppressor gene, which has been introduced as a biomarker for some specific cancers. In this study, we focus on MST1 expression levels in the WBC of PC patients, due to the inheritance pattern of PC. Methods: This case-control study was conducted in two groups (20 patients with PC and 20 healthy individuals). After RNA extraction and cDNA synthesis, quantitative Real-Time PCR was done in order to determine the MST1 expression level. GAPDH was selected as an internal control gene. Statistical analysis was performed using “Rotor-Gene Q series software 2.3.1” and “Rest 2.0.13 software”. Results: This study, carried out on 20 PC patients aged 50-70 and 20 healthy individuals shows that MST1 expression level in the WBC samples of PC patients is approximately 62% lower compared to normal individuals (P<0.01). Conclusion: Introducing the reduced expression level of MST1 as a prostate cancer biomarker requires complementary research. However, in this study, biomarker validation and potential of MST1 has been approved.
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