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AGO2 蛋白:miRNA 通路中的关键酶,作为肾上腺皮质癌的新型生物标志物。

AGO2 protein: a key enzyme in the miRNA pathway as a novel biomarker in adrenocortical carcinoma.

机构信息

School of Biomedical Engineering, University of Technology Sydney, Sydney, New South Wales, Australia.

NSW Health Pathology, Sydney, New South Wales, Australia.

出版信息

Endocr Relat Cancer. 2024 Nov 20;31(12). doi: 10.1530/ERC-24-0061. Print 2024 Dec 1.


DOI:10.1530/ERC-24-0061
PMID:39404265
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11623120/
Abstract

Adrenocortical carcinoma (ACC) is a rare and aggressive malignancy characterized by diagnostic challenges, high recurrence rates, and poor prognosis. This study explored the role of miRNA processing genes in ACC and their potential role as diagnostic and prognostic biomarkers. We analyzed the mRNA expression levels of miRNA machinery components (DROSHA, DGCR8, XPO5, RAN, DICER, TARBP2, and AGO2) utilizing mRNA-Seq data from The Cancer Genome Atlas (TCGA) and The Genotype-Tissue Expression (GTEx) projects. Additionally, protein levels were quantified in tissue samples from the Kolling Institute of Medical Research's tumor bank. Our results demonstrated that among all miRNA processing components, AGO2 exhibited significant overexpression in ACC compared to the normal adrenal cortex and benign adrenal adenoma (P < 0.001). Kaplan-Meier survival analysis indicated that higher AGO2 expression correlated with significantly worse overall survival in ACC patients (HR: 7.07, P < 0.001). Among 32 cancer types in TCGA, the prognostic significance of AGO2 was most prominent in ACC. This study is the first to report AGO2's potential as a diagnostic and prognostic biomarker in ACC, emphasizing its significance in ACC pathogenesis and potential application as a non-invasive liquid biopsy biomarker.

摘要

肾上腺皮质癌(ACC)是一种罕见且侵袭性强的恶性肿瘤,其诊断具有挑战性,复发率高,预后差。本研究探讨了 miRNA 加工基因在 ACC 中的作用及其作为诊断和预后生物标志物的潜在作用。我们利用癌症基因组图谱(TCGA)和基因型组织表达(GTEx)项目的 mRNA-Seq 数据分析了 miRNA 机器组件(DROSHA、DGCR8、XPO5、RAN、DICER、TARBP2 和 AGO2)的 mRNA 表达水平。此外,还在 Kolling 医学研究所肿瘤库的组织样本中定量了蛋白水平。我们的研究结果表明,在所有 miRNA 加工成分中,AGO2 在 ACC 中的表达显著高于正常肾上腺皮质和良性肾上腺腺瘤(P<0.001)。Kaplan-Meier 生存分析表明,AGO2 的高表达与 ACC 患者的总生存率显著降低相关(HR:7.07,P<0.001)。在 TCGA 中的 32 种癌症类型中,AGO2 的预后意义在 ACC 中最为显著。本研究首次报道了 AGO2 在 ACC 中作为诊断和预后生物标志物的潜力,强调了其在 ACC 发病机制中的重要性及其作为非侵入性液体活检生物标志物的潜在应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f075/11623120/24afb44449d0/ERC-24-0061fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f075/11623120/ebef43c6c861/ERC-24-0061fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f075/11623120/80cd6c1d44e8/ERC-24-0061fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f075/11623120/ebfbe78ea3d2/ERC-24-0061fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f075/11623120/e76cb9503b48/ERC-24-0061fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f075/11623120/662e4e2e8af0/ERC-24-0061fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f075/11623120/24afb44449d0/ERC-24-0061fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f075/11623120/ebef43c6c861/ERC-24-0061fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f075/11623120/80cd6c1d44e8/ERC-24-0061fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f075/11623120/ebfbe78ea3d2/ERC-24-0061fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f075/11623120/e76cb9503b48/ERC-24-0061fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f075/11623120/662e4e2e8af0/ERC-24-0061fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f075/11623120/24afb44449d0/ERC-24-0061fig6.jpg

相似文献

[1]
AGO2 protein: a key enzyme in the miRNA pathway as a novel biomarker in adrenocortical carcinoma.

Endocr Relat Cancer. 2024-12-1

[2]
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Front Immunol. 2025-4-17

[3]
Clinical and functional impact of TARBP2 over-expression in adrenocortical carcinoma.

Endocr Relat Cancer. 2013-7-4

[4]
Development and Validation of an m6A RNA Methylation Regulators-Based Signature for Predicting the Prognosis of Adrenocortical Carcinoma.

Front Endocrinol (Lausanne). 2021

[5]
Construction of a robust prognostic model for adult adrenocortical carcinoma: Results from bioinformatics and real-world data.

J Cell Mol Med. 2021-4

[6]
The role of microRNA deregulation in the pathogenesis of adrenocortical carcinoma.

Endocr Relat Cancer. 2011-10-27

[7]
Expression of FSCN1 and FOXM1 are associated with poor prognosis of adrenocortical carcinoma patients.

BMC Cancer. 2019-11-29

[8]
Serum miR-483-5p and miR-195 are predictive of recurrence risk in adrenocortical cancer patients.

Endocr Relat Cancer. 2013-7-5

[9]
Reduced expression of ferroportin1 and ceruloplasmin predicts poor prognosis in adrenocortical carcinoma.

J Trace Elem Med Biol. 2019-7-23

[10]
Analysis of m6A-Related Signatures in the Tumor Immune Microenvironment and Identification of Clinical Prognostic Regulators in Adrenocortical Carcinoma.

Front Immunol. 2021

本文引用的文献

[1]
Supportive therapies in patients with advanced adrenocortical carcinoma submitted to standard EDP-M regimen.

Endocrine. 2022-9

[2]
The Diagnostic, Prognostic and Therapeutic Role of miRNAs in Adrenocortical Carcinoma: A Systematic Review.

Biomedicines. 2021-10-20

[3]
Adrenocortical Carcinoma: A Case of Missed Diagnosis.

Cureus. 2021-4-1

[4]
TNMplot.com: A Web Tool for the Comparison of Gene Expression in Normal, Tumor and Metastatic Tissues.

Int J Mol Sci. 2021-3-5

[5]
ChrXq27.3 miRNA cluster functions in cancer development.

J Exp Clin Cancer Res. 2021-3-25

[6]
Visualizing and interpreting cancer genomics data via the Xena platform.

Nat Biotechnol. 2020-6

[7]
Surgery for adrenocortical carcinoma: When and how?

Best Pract Res Clin Endocrinol Metab. 2020-5

[8]
Non-Coding RNAs in Adrenocortical Cancer: From Pathogenesis to Diagnosis.

Cancers (Basel). 2020-2-17

[9]
Dysregulation of the miRNA biogenesis components DICER1, DROSHA, DGCR8 and AGO2 in clear cell renal cell carcinoma in both a Korean cohort and the cancer genome atlas kidney clear cell carcinoma cohort.

Oncol Lett. 2019-10

[10]
European Society of Endocrinology Clinical Practice Guidelines on the management of adrenocortical carcinoma in adults, in collaboration with the European Network for the Study of Adrenal Tumors.

Eur J Endocrinol. 2018-10-1

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