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miR-21和MEG-2的特征及其与乳腺癌中TGF-β信号传导的相关性。

Signature of miR-21 and MEG-2 and their correlation with TGF-β signaling in breast cancer.

作者信息

Desouky E M, Khaliefa A K, Hozayen W G, Shaaban S M, Hasona N A

机构信息

Department of Biochemistry, Faculty of Science, 158406Beni-Suef University, Beni-Suef, Egypt.

Department of Oncology, Faculty of Medicine, 158411Beni-Suef University, Beni-Suef, Egypt.

出版信息

Hum Exp Toxicol. 2023 Jan-Dec;42:9603271231159799. doi: 10.1177/09603271231159799.

Abstract

Breast cancer is highly prevalent and considered the main challenge to public health among females in Egypt as in other countries. MicroRNA-21 (miR-21) and MEG-2 are noncoding RNA attributed to their aberrant expression in several diseases, including breast cancer. This study aimed to assess the reliability of serum expression levels of miR-21 and MEG-2 in discriminating stages of breast cancer and scrutinize their correlations with the targeted transforming growth factor-beta (TGF-β) expression. One hundred and 30 participants whose ages ranged from 28 to 62 years were included in this study, divided into one hundred breast cancer patients and 30 healthy participants. miR-21 and TGF-β expression levels showed upregulation in patients with BC and elevated miR-21/TGF-β levels consistent with the BC stage. In addition, LncRNA (MEG-2) showed down-regulation in patients with BC. MEG-2 expression levels revealed a gradual decrease consistent with the BC stage. In addition, a negative relationship between the MEG-2 and the miR-21 and TGF-β differential expression was also noticed. This study suggested that miR-21 and MEG-2 can be used as prospective diagnostic biomarkers and emphasized the crucible role of TGF-β as therapeutic targets for BC.

摘要

乳腺癌非常普遍,在埃及和其他国家一样,被认为是女性公共卫生面临的主要挑战。微小RNA-21(miR-21)和MEG-2是非编码RNA,它们在包括乳腺癌在内的多种疾病中表达异常。本研究旨在评估血清中miR-21和MEG-2表达水平在区分乳腺癌分期方面的可靠性,并研究它们与靶向转化生长因子-β(TGF-β)表达的相关性。本研究纳入了130名年龄在28至62岁之间的参与者,分为100名乳腺癌患者和30名健康参与者。miR-21和TGF-β的表达水平在乳腺癌患者中上调,且miR-21/TGF-β水平随乳腺癌分期升高。此外,长链非编码RNA(MEG-2)在乳腺癌患者中表达下调。MEG-2的表达水平随乳腺癌分期逐渐降低。此外,还发现MEG-2与miR-21和TGF-β差异表达之间存在负相关。本研究表明,miR-21和MEG-2可作为潜在的诊断生物标志物,并强调了TGF-β作为乳腺癌治疗靶点的关键作用。

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