circ-HIPK3、circ-PVT1、miR-25和miR-149在乳腺癌放射敏感性中的表观遗传调控

IF 2.8 4区 医学 Q2 PATHOLOGY
Elahe Abdollahi, Hossein Mozdarani
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引用次数: 0

摘要

在对诊断为癌症(BC)的个体进行放射治疗(RT)之前,评估细胞的放射敏感性可以促进选择适当的治疗方案,并最大限度地降低接受放射治疗的患者的不良副作用发生率。在这项研究中,从60名被诊断为侵袭性导管癌(IDC)癌症的女性身上采集了血液样本。患者的平均年龄为47±9.93岁。此外,该研究纳入了20名健康女性,平均年龄为44.43±6.7岁。进行标准G2测定以预测细胞对辐射的反应。在60个样本中,G2检测确定了20名表现出放射敏感性的癌症乳腺癌患者。因此,最终对两个同等的队列进行了分子研究,每个队列包括20名受试者,一名具有细胞放射敏感性,另一名没有细胞放射敏感性。使用定量聚合酶链式反应(qPCR)评估外周血单核细胞(PBMC)中miR-149、miR-25、circ-PVT1和circ-HIPK3的表达水平。受试者操作特征(ROC)曲线用于评估RNA的敏感性和特异性。使用二元逻辑回归进行分析,以研究RNA与BC患者的BC和细胞放射敏感性(CR)之间的关系。研究结果显示,在诊断为BC的个体中,Circ-HIPK3和Circ-PVT1显著上调。发现Circ-HIPK3和Circ-PVT1的水平与BC患者的CR直接相关。ROC曲线的分析表明,circ-HIPK3和circ-PVT1在准确预测BC患者的BC和CR方面表现出良好的特异性和敏感性。二元逻辑回归分析的结果表明,circ-HIPK3和circ-PVT1是BC和CR的有效预测因子。ROC曲线和二元逻辑返回分析提供了证据,证明miR-25仅是BC患者的可靠预测因子。我们的研究表明,circ-HIPK3、circ-PVT1和miR-25可能参与BC调节过程。环状RNA Circ-HIPK3和Circ-PVT1,以及miR-25,以及其他重要的生物标志物,可能成为预测BC的有前途的生物标志。此外,Circ-HIPK3和Circ-PVT1有潜力作为预测BC患者CR的生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Epigenetic regulation of circ-HIPK3, circ-PVT1, miR-25, and miR-149 in radiosensitivity of breast cancer

Assessing the radiosensitivity of cells before administering radiation therapy (RT) to individuals diagnosed with breast cancer (BC) can facilitate the selection of appropriate treatment regimens and minimize the incidence of adverse side effects in patients undergoing radiation exposure.

In this research, blood samples were obtained from 60 women who had been diagnosed with Invasive Ductal Carcinoma (IDC) Breast Cancer. The average age of the patients was 47 ± 9.93. Additionally, the study incorporated 20 healthy women, with an average age of 44.43 ± 6.7. A standard G2 assay was conducted to predict the cellular response to radiation. Out of the 60 samples, the G2 assay identified 20 patients with breast cancer who exhibited radiosensitivity. Hence, molecular investigations were ultimately conducted on two equivalent cohorts comprising 20 subjects each, one with and the other without cellular radiosensitivity. The expression levels of miR-149, miR-25, circ-PVT1, and circ-HIPK3 in peripheral blood mononuclear cells (PBMCs) were evaluated using quantitative polymerase chain reaction (qPCR). Receiver Operating Characteristic (ROC) curves were used to evaluate the sensitivity and specificity of the RNAs. An analysis using binary logistic regression was performed to investigate the relationship between RNAs and both BC and cellular radiosensitivity (CR) in patients with BC.

The findings revealed a significant upregulation of Circ-HIPK3 and circ-PVT1 in individuals diagnosed with BC. The levels of Circ-HIPK3 and Circ-PVT1 were found to be directly associated with CR in BC patients. The analysis of the ROC curve demonstrated that circ-HIPK3 and circ-PVT1 exhibit favorable specificity and sensitivity in accurately predicting both BC and CR in patients with BC. The findings from the binary logistic regression analysis demonstrated that circ-HIPK3 and circ-PVT1 were effective predictors of both BC and CR. The ROC curve and binary logistic regression analyses provide evidence that miR-25 is a reliable predictor for BC patients exclusively.

Our research has demonstrated that circ-HIPK3, circ-PVT1, and miR-25 may be involved in BC regulatory processes. The circular RNAs Circ-HIPK3 and circ-PVT1, as well as miR-25, among other significant biomarkers, could potentially serve as promising biomarkers for predicting BC. Furthermore, Circ-HIPK3 and circ-PVT1 have the potential to serve as biomarkers for predicting CR in BC patients.

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来源期刊
CiteScore
8.90
自引率
0.00%
发文量
78
审稿时长
11.5 weeks
期刊介绍: Under new editorial leadership, Experimental and Molecular Pathology presents original articles on disease processes in relation to structural and biochemical alterations in mammalian tissues and fluids and on the application of newer techniques of molecular biology to problems of pathology in humans and other animals. The journal also publishes selected interpretive synthesis reviews by bench level investigators working at the "cutting edge" of contemporary research in pathology. In addition, special thematic issues present original research reports that unravel some of Nature''s most jealously guarded secrets on the pathologic basis of disease. Research Areas include: Stem cells; Neoangiogenesis; Molecular diagnostics; Polymerase chain reaction; In situ hybridization; DNA sequencing; Cell receptors; Carcinogenesis; Pathobiology of neoplasia; Complex infectious diseases; Transplantation; Cytokines; Flow cytomeric analysis; Inflammation; Cellular injury; Immunology and hypersensitivity; Athersclerosis.
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