Evaluation of the Effect of Radiotherapy on CCL5/miR-214 -3p/MALAT1 Genes Expression in Blood Samples of Breast Cancer Patients.

IF 1.5 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Fazlollah Shokri, Hossein Mozdarani, Mir Davood Omrani
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引用次数: 0

Abstract

Current cancer therapies include chemotherapy, radiation therapy, immunotherapy, and surgery. Despite these treatment methods, a major point in cancer treatment is early detection. RNAs (mRNA, miRNAs, and LncRNA) can be used as markers to improve cancer diagnosis and treatment. This research examined how radiotherapy affected CCL5, miR-214, and MALAT-1 gene expression in the immune pathway in peripheral blood samples from radiation therapy-treated breast cancer patients. Before and after radiotherapy, peripheral blood was collected from 15 patients in four steps. Blood samples were collected in an outpatient facility from 20 healthy female volunteers with no history of malignant or inflammatory conditions. RNA was extracted from the blood samples and cDNA was synthesized. CCL5, miR-214, and MALAT-1 gene expression were determined by real-time polymerase chain reaction (RT-PCR). CCL5 protein levels in the serum were determined in 80 samples (60 BC and 20 healthy controls) using Quantikine Enzyme-Linked Immunosorbent Assay (ELISA) kits (R&D Systems). The data were then statistically evaluated. There was a significant difference between CCL5 levels in tumoral and adjacent normal blood samples (p < 0.05). The results also show that the level of gene expression and serum concentration of CCL5 protein in different phases of radiotherapy is significantly different. On the other hand, the expression level of the miR-214 gene was significantly decreased in patients compared to the control group, but this decrease was not significant for the MALAT-1 gene (p< 0.05). Also, after each stage of radiotherapy, the expression level of these two genes showed a decrease, but in the fourth week after radiotherapy, this decrease was significant (p< 0.05). Radiotherapy is associated with a decrease in the expression of miR-214 and MALAT-1, as a result, an increase in the expression of CCL5. An increase in the concentration of CCL5 protein is accompanied by an increase in the level of monocytes, which ultimately causes the infiltration of macrophages and can ultimately cause cancer recurrence. It is suggested that these genes can probably be used as diagnostic and therapeutic radiotherapy markers in breast cancer.

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放疗对乳腺癌患者血液样本中CCL5/miR-214 -3p/MALAT1基因表达的影响
目前的癌症治疗包括化疗、放射治疗、免疫治疗和手术。尽管有这些治疗方法,但癌症治疗的一个重点是早期发现。rna (mRNA, mirna, LncRNA)可以作为标志物来改善癌症的诊断和治疗。本研究考察了放疗如何影响放疗后乳腺癌患者外周血样本中免疫通路中的CCL5、miR-214和MALAT-1基因表达。15例患者放疗前后分四步采集外周血。血液样本是在一家门诊机构收集的,来自20名没有恶性或炎症病史的健康女性志愿者。从血样中提取RNA,合成cDNA。实时聚合酶链反应(RT-PCR)检测CCL5、miR-214和MALAT-1基因表达。使用定量酶联免疫吸附试验(ELISA)试剂盒(R&D Systems)测定80个样本(60例BC和20例健康对照)血清中的CCL5蛋白水平。然后对数据进行统计评估。肿瘤标本与邻近正常标本CCL5水平差异有统计学意义(p < 0.05)。结果还表明,CCL5基因表达水平和血清CCL5蛋白浓度在不同放疗阶段存在显著差异。另一方面,与对照组相比,患者miR-214基因的表达水平明显下降,而MALAT-1基因的表达水平下降不显著(p< 0.05)。同时,在每个放疗阶段后,这两个基因的表达水平均呈下降趋势,但在放疗后第4周,这两个基因的表达水平下降幅度显著(p< 0.05)。放疗与miR-214和MALAT-1表达降低相关,从而导致CCL5表达增加。CCL5蛋白浓度的升高伴随着单核细胞水平的升高,最终引起巨噬细胞的浸润,最终可引起癌症复发。提示这些基因可能用作乳腺癌的诊断和治疗性放疗标志物。
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来源期刊
CiteScore
3.60
自引率
0.00%
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0
期刊介绍: The International Journal of Molecular and Cellular Medicine (IJMCM) is a peer-reviewed, quarterly publication of Cellular and Molecular Biology Research Center (CMBRC), Babol University of Medical Sciences, Babol, Iran. The journal covers all cellular & molecular biology and medicine disciplines such as the genetic basis of disease, biomarker discovery in diagnosis and treatment, genomics and proteomics, bioinformatics, computer applications in human biology, stem cells and tissue engineering, medical biotechnology, nanomedicine, cellular processes related to growth, death and survival, clinical biochemistry, molecular & cellular immunology, molecular and cellular aspects of infectious disease and cancer research. IJMCM is a free access journal. All open access articles published in IJMCM are distributed under the terms of the Creative Commons Attribution CC BY. The journal doesn''t have any submission and article processing charges (APCs).
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