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p16启动子甲基化、BRAFV600E突变及ETS1表达测定对甲状腺乳头状癌预后及高危患者选择的意义

Implication of p16 Promoter Methylation, the BRAFV600E Mutation, and ETS1 Expression Determination on Papillary Thyroid Carcinoma Prognosis and High-Risk Patients' Selection.

作者信息

Stojanović Novković Stefana, Šelemetjev Sonja, Krajnović Milena, Božović Ana, Kožik Bojana, Prosenc Zmrzljak Uršula, Išić Denčić Tijana

机构信息

Department of Endocrinology and Radioimmunology, Institute for the Application of Nuclear Energy-INEP, University of Belgrade, Banatska 31b, Zemun, 11080 Belgrade, Serbia.

Laboratory for Radiobiology and Molecular Genetics, Vinča Institute of Nuclear Sciences, National Institute of the Republic of Serbia, University of Belgrade, Mike Petrovića Alasa 12-14, Vinča, 11351 Belgrade, Serbia.

出版信息

Biomedicines. 2025 Jun 27;13(7):1583. doi: 10.3390/biomedicines13071583.

Abstract

: Papillary thyroid carcinoma (PTC) is the most common malignancy of the endocrine system, characterized by various molecular alterations. This study evaluates the relationship between p16 promoter methylation status, BRAFV600E mutation presence, and ETS1 (E26 transformation-specific) expression, aiming to better understand their clinical significance and to enhance the risk stratification of PTC patients. : p16 promoter methylation was analyzed by methylation-specific PCR (MSP), BRAFV600E by mutant allele-specific PCR amplification (MASA), ETS1 mRNA expression by quantitative PCR (qPCR), ETS1 protein expression by immunohistochemistry (IHC), and Western blot. All tested factors were further associated with the occurrence of unfavorable clinicopathological data of the patients. : While p16 methylation did not correlate with adverse clinical parameters or BRAFV600E mutation presence, it was significantly associated with the increased ETS1 mRNA levels. Combined p16 methylation with high ETS1 protein levels was significantly associated with advanced pT and pTNM stages. BRAFV600E-mutated PTC cases with p16 methylation showed increased mRNA and protein ETS1 expression. : Therefore, although p16 methylation could not be used as a standalone prognostic marker, its association with elevated ETS1 levels points to its potential involvement in tumor progression and adverse clinical outcomes, particularly in BRAFV600E-mutated PTCs. Deeper insights into these interactions may enhance PTC prognosis and the selection of high-risk patients.

摘要

甲状腺乳头状癌(PTC)是内分泌系统最常见的恶性肿瘤,具有多种分子改变。本研究评估p16启动子甲基化状态、BRAFV600E突变的存在与ETS1(E26转化特异性)表达之间的关系,旨在更好地理解它们的临床意义并加强PTC患者的风险分层。通过甲基化特异性PCR(MSP)分析p16启动子甲基化,通过突变等位基因特异性PCR扩增(MASA)分析BRAFV600E,通过定量PCR(qPCR)分析ETS1 mRNA表达,通过免疫组织化学(IHC)和蛋白质印迹分析ETS1蛋白表达。所有检测因素均进一步与患者不良临床病理数据的发生相关。虽然p16甲基化与不良临床参数或BRAFV600E突变的存在无关,但它与ETS1 mRNA水平升高显著相关。p16甲基化与高ETS1蛋白水平相结合与晚期pT和pTNM分期显著相关。具有p16甲基化的BRAFV600E突变PTC病例显示ETS1 mRNA和蛋白表达增加。因此,虽然p16甲基化不能用作独立的预后标志物,但其与ETS1水平升高的关联表明它可能参与肿瘤进展和不良临床结局,特别是在BRAFV600E突变的PTC中。对这些相互作用的更深入了解可能会改善PTC的预后并选择高危患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d9a/12292734/54fd7f625774/biomedicines-13-01583-g001.jpg

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