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神经胶质瘤的分子生物标志物

Molecular Biomarkers of Glioma.

作者信息

Rajakaruna Punsasi, Rios Stella, Elnahas Hana, Villanueva Ashley, Uribe David, Leslie Sophia, Abbas Walaa A, Barroso Larissa, Oyervides Stephanie, Persans Michael, Innis-Whitehouse Wendy, Keniry Megan

机构信息

School of Integrative Biological and Chemical Sciences, The University of Texas Rio Grande Valley, 1201 W. University Dr., Edinburg, TX 78539, USA.

Burrell College of Osteopathic Medicine, 3501 Arrowhead Dr, Las Cruces, NM 88001, USA.

出版信息

Biomedicines. 2025 May 26;13(6):1298. doi: 10.3390/biomedicines13061298.


DOI:10.3390/biomedicines13061298
PMID:40564017
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12189432/
Abstract

In this review, we discuss how mutations in glioma are associated with prognosis and treatment efficacy. A fascinating characteristic of glioma and all cancers is that while common growth and developmental pathways are altered, the characteristic mutations are distinct depending on the specific type of tumor with concomitant prognoses. Next-generation sequencing, precision medicine, and artificial intelligence are boosting the employment of molecular biomarkers in cancer diagnosis and treatment. Understanding the biological underpinnings of distinct mutations on critical signaling pathways is crucial for developing novel therapies for glioma.

摘要

在本综述中,我们讨论了胶质瘤中的突变如何与预后和治疗效果相关联。胶质瘤以及所有癌症的一个引人入胜的特征是,虽然常见的生长和发育途径发生了改变,但特征性突变因肿瘤的具体类型以及随之而来的预后情况而异。下一代测序、精准医学和人工智能正在推动分子生物标志物在癌症诊断和治疗中的应用。了解关键信号通路中不同突变的生物学基础对于开发胶质瘤的新型疗法至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f3d2/12189432/93efc3555355/biomedicines-13-01298-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f3d2/12189432/06e3c4a54af4/biomedicines-13-01298-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f3d2/12189432/93efc3555355/biomedicines-13-01298-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f3d2/12189432/06e3c4a54af4/biomedicines-13-01298-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f3d2/12189432/93efc3555355/biomedicines-13-01298-g002.jpg

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本文引用的文献

[1]
Discovery of mutated oncodriver genes associated with glioblastoma originated from stem cells of subventricular zone through whole exome sequence profile analysis, and drug repurposing.

Heliyon. 2025-1-16

[2]
Loss of Kmt2c or Kmt2d primes urothelium for tumorigenesis and redistributes KMT2A-menin to bivalent promoters.

Nat Genet. 2025-1

[3]
ATRX mutation modifies the DNA damage response in glioblastoma multiforme tumor cells and enhances patient prognosis.

Medicine (Baltimore). 2025-1-10

[4]
IDH Mutations in Glioma: Molecular, Cellular, Diagnostic, and Clinical Implications.

Biology (Basel). 2024-10-30

[5]
NF1 expression profiling in IDH-wildtype glioblastoma: genomic associations and survival outcomes.

Acta Neuropathol Commun. 2024-10-29

[6]
Pre-operative dual-time-point [F]FET PET differentiates CDKN2A/B loss and PIK3CA mutation status in adult-type diffuse glioma: a single-center prospective study.

Eur J Nucl Med Mol Imaging. 2025-1

[7]
The modification role and tumor association with a methyltransferase: KMT2C.

Front Immunol. 2024

[8]
Diagnostic and Practical Challenges in Applying National Comprehensive Cancer Network Guidelines for Suspected Pathogenic TP53 Mosaicism.

JCO Precis Oncol. 2024-7

[9]
Integrative analysis of genomic and epigenomic regulation reveals miRNA mediated tumor heterogeneity and immune evasion in lower grade glioma.

Commun Biol. 2024-7-6

[10]
IMPDH Inhibition Decreases TERT Expression and Synergizes the Cytotoxic Effect of Chemotherapeutic Agents in Glioblastoma Cells.

Int J Mol Sci. 2024-5-30

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