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环状 FOXO3 和 miR-23a 在乳腺癌放射敏感性中的作用。

Role of circ-FOXO3 and miR-23a in radiosensitivity of breast cancer.

机构信息

Department of Medical Genetics, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.

Unit of Personalized Medicine, Department of Epidemiology, University Medical Center Groningen, Groningen, The Netherlands.

出版信息

Breast Cancer. 2023 Sep;30(5):714-726. doi: 10.1007/s12282-023-01463-4. Epub 2023 May 24.

Abstract

Identifying the radiosensitivity of cells before radiotherapy (RT) in breast cancer (BC) patients allows appropriate switching between routinely used treatment regimens and reduces adverse side effects in exposed patients. In this study, blood was collected from 60 women diagnosed with Invasive Ductal Carcinoma (IDC) BC and 20 healthy women. To predict cellular radiosensitivity, a standard G2-chromosomal assay was performed. From these 60 samples, 20 BC patients were found to be radiosensitive based on the G2 assay. Therefore, molecular studies were finally performed on two equal groups (20 samples each) of patients with and without cellular radiosensitivity. QPCR was performed to examine the expression levels of circ-FOXO3 and miR-23a in peripheral blood mononuclear cells (PBMCs) and RNA sensitivity and specificity were determined by plotting Receiver Operating Characteristic (ROC) curves. Binary logistic regression was performed to identify RNA involvement in BC and cellular radiosensitivity (CR) in BC patients. Meanwhile, qPCR was used to compare differential RNA expression in the radiosensitive MCF-7 and radioresistant MDA-MB-231 cell lines. An annexin -V FITC/PI binding assay was used to measure cell apoptosis 24 and 48 h after 2 Gy, 4 Gy, and 8 Gy gamma-irradiation. Results indicated that circ-FOXO3 was downregulated and miR-23a was upregulated in BC patients. RNA expression levels were directly associated with CR. Cell line results showed that circ-FOXO3 overexpression induced apoptosis in the MCF-7 cell line and miR-23a overexpression inhibited apoptosis in the MDA-MB-231 cell line. Evaluation of the ROC curves revealed that both RNAs had acceptable specificity and sensitivity in predicting CR in BC patients. Binary logistic regression showed that both RNAs were also successful in predicting breast cancer. Although only circ-FOXO3 has been shown to predict CR in BC patients, circ-FOXO3 may function as a tumor suppressor and miR-23a may function as oncomiR in BC. Circ-FOXO3 and miR-23a may be promising potential biomarkers for BC prediction. Furthermore, Circ-FOXO3 could be a potential biomarker for predicting CR in BC patients.

摘要

在乳腺癌(BC)患者进行放射治疗(RT)之前,确定细胞的放射敏感性可以使常规治疗方案适当切换,并减少暴露患者的不良副作用。在这项研究中,采集了 60 名被诊断患有浸润性导管癌(IDC)BC 和 20 名健康女性的血液。为了预测细胞放射敏感性,进行了标准的 G2 染色体测定。在这 60 个样本中,根据 G2 测定有 20 名 BC 患者被认为是放射敏感的。因此,最终对有和没有细胞放射敏感性的患者各进行了两组(每组 20 个样本)的分子研究。进行 QPCR 以检查外周血单核细胞(PBMC)中 circ-FOXO3 和 miR-23a 的表达水平,并通过绘制接收器操作特征(ROC)曲线来确定 RNA 的敏感性和特异性。进行二元逻辑回归以鉴定 RNA 在 BC 中的作用以及 BC 患者的细胞放射敏感性(CR)。同时,使用 qPCR 比较放射敏感的 MCF-7 和放射抵抗的 MDA-MB-231 细胞系中差异 RNA 的表达。用膜联蛋白-V FITC/PI 结合测定法在 2 Gy、4 Gy 和 8 Gy γ照射后 24 和 48 小时测量细胞凋亡。结果表明,BC 患者中 circ-FOXO3 下调,miR-23a 上调。RNA 表达水平与 CR 直接相关。细胞系结果表明,circ-FOXO3 过表达诱导 MCF-7 细胞系凋亡,miR-23a 过表达抑制 MDA-MB-231 细胞系凋亡。ROC 曲线的评估表明,这两种 RNA 在预测 BC 患者的 CR 方面均具有可接受的特异性和敏感性。二元逻辑回归表明,这两种 RNA 也成功地预测了乳腺癌。虽然仅 circ-FOXO3 已被证明可预测 BC 患者的 CR,但 circ-FOXO3 可能作为肿瘤抑制因子,miR-23a 可能作为 BC 中的致癌 miRNA。circ-FOXO3 和 miR-23a 可能是 BC 预测的有前途的潜在生物标志物。此外,circ-FOXO3 可能是预测 BC 患者 CR 的潜在生物标志物。

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