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基于宫颈巴氏刷样本中 DNA 甲基化分析的子宫内膜癌检测。

Endometrial Cancer Detection by DNA Methylation Analysis in Cervical Papanicolaou Brush Samples.

机构信息

Department of Gynecology, Guangdong Women and Children Hospital, Guangzhou, China.

Maternal and Child Health Research Institute, Translational Medicine Center, Guangdong Women and Children Hospital, Guangzhou, China.

出版信息

Technol Cancer Res Treat. 2024 Jan-Dec;23:15330338241242637. doi: 10.1177/15330338241242637.

Abstract

Endometrial cancer (EC) is the leading gynecological cancer worldwide, yet current EC screening approaches are not satisfying. The purpose of this retrospective study was to evaluate the feasibility and capability of DNA methylation analysis in cervical Papanicolaou (Pap) brush samples for EC detection. We used quantitative methylation-sensitive PCR (qMS-PCR) to determine the methylation status of candidate genes in EC tissue samples, as well as cervical Pap brushes. The ability of RASSF1A and HIST1H4F to serve as diagnostic markers for EC was then examined in cervical Pap brush samples from women with endometrial lesions of varying degrees of severity. Methylated RASSF1A and HIST1H4F were found in EC tissues. Further, methylation of the two genes was also observed in cervical Pap smear samples from EC patients. Methylation levels of RASSF1A and HIST1H4F increased as endometrial lesions progressed, and cervical Pap brush samples from women affected by EC exhibited significantly higher levels of methylated RASSF1A and HIST1H4F compared to noncancerous controls ( < .001). Receiver operating characteristic (ROC) curves and area under the curve (AUC) analyses revealed RASSF1A and HIST1H4F methylation with a combined AUC of 0.938 and 0.951 for EC/pre-EC detection in cervical Pap brush samples, respectively. These findings demonstrate that DNA methylation analysis in cervical Pap brush samples may be helpful for EC detection, broadening the scope of the commonly used cytological screening. Our proof-of-concept study provides new insights into the field of clinical EC diagnosis.

摘要

子宫内膜癌(EC)是全球领先的妇科癌症,但目前的 EC 筛查方法并不令人满意。本回顾性研究的目的是评估 DNA 甲基化分析在宫颈巴氏涂片样本中用于 EC 检测的可行性和能力。我们使用定量甲基化敏感 PCR(qMS-PCR)来确定 EC 组织样本以及宫颈巴氏涂片样本中候选基因的甲基化状态。然后,在来自不同严重程度子宫内膜病变的女性的宫颈巴氏涂片样本中,检查 RASSF1A 和 HIST1H4F 作为 EC 诊断标志物的能力。在 EC 组织中发现了甲基化的 RASSF1A 和 HIST1H4F。此外,还观察到这两个基因在 EC 患者的宫颈巴氏涂片样本中也发生了甲基化。随着子宫内膜病变的进展,RASSF1A 和 HIST1H4F 的甲基化水平增加,受 EC 影响的女性的宫颈巴氏涂片样本中甲基化的 RASSF1A 和 HIST1H4F 水平明显高于非癌对照(<0.001)。接收者操作特征(ROC)曲线和曲线下面积(AUC)分析显示,在宫颈巴氏涂片样本中,RASSF1A 和 HIST1H4F 甲基化的 AUC 分别为 0.938 和 0.951,用于 EC/前 EC 检测。这些发现表明,宫颈巴氏涂片样本中的 DNA 甲基化分析可能有助于 EC 的检测,拓宽了常用细胞学筛查的范围。我们的概念验证研究为 EC 临床诊断领域提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1417/11005493/1ecd64c2e0b7/10.1177_15330338241242637-fig1.jpg

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