与非功能性垂体神经内分泌肿瘤患者侵袭性和复发有关的 MiRNA 特征--一项在单一三级中心开展的试点研究。

Emiliya Nikolova, Anelia Nankova, Silvia Kalenderova, Bilyana Georgieva, Asen Hadzhiyanev, Stoyan Bichev, Alexey Savov, Albena Todorova, Vanyo Mitev, Atanaska Elenkova
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引用次数: 0

摘要

目的:这项初步研究旨在分析和鉴定保加利亚非功能性垂体神经内分泌肿瘤(NFPitNET)患者体内表达不同的miRNA。研究还确定了失调的 miRNA 与肿瘤侵袭性、复发性和大小之间的关系:方法:选取 20 例非功能性垂体神经内分泌肿瘤患者,收集新鲜垂体肿瘤组织。用miRNAeasy mini试剂盒分离含有miRNA的RNA,并用LNA miRNA Cancer Focus PCR Panel(Qiagen公司)进行实时定量PCR分析:结果:与非侵袭性NFPitNET相比,侵袭性NFPitNET中有三个miRNA(miR-210-3p、miR-149-3p和miR-29b-3p)表达失调。四种miRNA特征--miRNA-17、miR-19、miR-106a和miR-20的差异表达与患者的复发有关:在这项前瞻性试验研究中,我们筛选出了与非功能性垂体神经内分泌肿瘤的侵袭性和复发相关的独特 miRNA 表达谱。此外,一些被选中的 miRNAs 还是首次在该病患者中被报道,从而揭示了垂体发病机制的分子机制。已鉴定的 miRNAs 具有作为生物标志物的潜力,值得在更大的群体中进一步研究,以验证其临床适用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MiRNA Signatures Related to Invasiveness and Recurrence in Patients With Non-Functioning Pituitary Neuroendocrine Tumors.

Purpose: This preliminary study aimed to analyze and identify differentially expressed miRNAs in Bulgarian patients with non-functioning pituitary neuroendocrine tumors (NFPitNET). The relationship between deregulated miRNAs and tumor invasiveness, recurrence, and size was determined.

Methods: Twenty patients with NFPitNET were selected and fresh pituitary tumor tissues were collected. RNA containing miRNAs were isolated using miRNAeasy mini kit and analyzed by quantitative real-time polymerase chain reaction (PCR) using LNA miRNA Cancer-Focus PCR Panel (Qiagen).

Results: Three miRNAs (miR-210-3p, miR-149-3p, and miR-29b-3p) were deregulated in invasive compared to non-invasive NFPitNETs. Differential expression of four-miRNA signatures - miRNA-17, miR-19, miR-106a, and miR-20, correlated with patient recurrence.

Conclusion: This prospective pilot study selected a unique miRNA expression profile, that correlates with invasiveness and recurrence in non-functioning pituitary neuroendocrine tumors. Moreover, some of the selected miRNAs are reported for the first time in patients with this disease, shedding light on the molecular mechanisms involved in pituitary pathogenesis. The identified miRNAs demonstrate potential as biomarkers, deserving further investigation in a larger cohort to validate their clinical applicability.

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