Expression Pattern Study of miR-200a and XIAP Gene in the Non-small Cell Lung Cancer Patients’ Blood

Q2 Biochemistry, Genetics and Molecular Biology
Tara Fereydouni, Seyed Jalal Zargar, Sharareh Seifi, Mojgan Sheikhpour
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Abstract

Background: In non-small cell lung cancer (NSCLC), miR-200a plays a significant role in apoptosis. One of the genes involved in this pathway is XIAP, which has been shown anti-apoptotic activity. Research has indicated a significant association between miR-200a and the XIAP gene in this pathway. The present study investigated the expression profiles of miR-200a and the XIAP gene in NSCLC patients compared to normal individuals, as well as cancer cells compared to normal and apoptosis-inducing conditions.

Methods: In this study, 40 blood specimens were collected from NSCLC patients and 40 from healthy individuals. After isolating plasma and peripheral blood mononuclear cells from these samples, we analyzed the miR-200a and XIAP gene expression levels using real-time PCR. Subsequently, normal and lung cancer cells were treated with paclitaxel as a model of apoptosis. The antiproliferative effects and induction of apoptosis were then evaluated using the MTT and flow cytometry assays, respectively. Finally, the expression patterns of miR-200a and the XIAP gene were investigated through a real-time PCR method.

Results: Results indicated that the miR-200a expression level was lower in NSCLC patients than in healthy ones, while the expression level of XIAP gene increased in the NSCLC Patients’ blood. The MTT and flow cytometry results demonstrated a decreased proliferation and increased apoptosis rates in two lung line cells (A549 and MRC5) treated with paclitaxel. XIAP expression level also decreased in A549 cells treated with paclitaxel compared to untreated A549 cells.

Conclusion: MiR-200a may be associated with the XIAP gene expression and the induction of the apoptosis pathway in NSCLC.

miR-200a和XIAP基因在非小细胞肺癌患者血液中的表达模式研究
背景:在非小细胞肺癌(NSCLC)中,miR-200a在细胞凋亡中起重要作用。参与该途径的基因之一是XIAP,它已被证明具有抗凋亡活性。研究表明,miR-200a与该通路中的XIAP基因存在显著关联。本研究研究了miR-200a和XIAP基因在非小细胞肺癌患者中与正常人相比的表达谱,以及癌细胞与正常和凋亡诱导条件下的表达谱。方法:本研究采集了40例非小细胞肺癌患者和40例健康人的血液标本。从这些样本中分离血浆和外周血单个核细胞后,我们使用实时PCR分析miR-200a和XIAP基因表达水平。随后,用紫杉醇处理正常细胞和肺癌细胞作为细胞凋亡模型。然后分别用MTT和流式细胞术评价其抗增殖作用和诱导凋亡作用。最后,通过real-time PCR方法研究miR-200a和XIAP基因的表达模式。结果:结果显示,miR-200a在NSCLC患者中的表达水平低于健康患者,而XIAP基因在NSCLC患者血液中的表达水平升高。MTT和流式细胞术结果显示,紫杉醇治疗后,两种肺系细胞(A549和MRC5)的增殖降低,凋亡率升高。与未处理的A549细胞相比,紫杉醇处理的A549细胞中XIAP的表达水平也有所下降。结论:MiR-200a可能与NSCLC中XIAP基因的表达及凋亡通路的诱导有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Iranian Biomedical Journal
Iranian Biomedical Journal Biochemistry, Genetics and Molecular Biology-Biochemistry, Genetics and Molecular Biology (all)
CiteScore
3.20
自引率
0.00%
发文量
42
审稿时长
8 weeks
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