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NEIL家族在癌症中作用的研究进展

Research progress on the role of the NEIL family in cancer.

作者信息

Chen Yinghan, Ma Muyun, Zou Aixue, Wang Xinjia, Dong Weiwei

机构信息

Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang, China.

Department of Rheumatology and Immunology, Beijing Hospital, Chinese Academy of Medical Sciences, Beijing, China.

出版信息

Front Cell Dev Biol. 2025 Jul 21;13:1612329. doi: 10.3389/fcell.2025.1612329. eCollection 2025.


DOI:10.3389/fcell.2025.1612329
PMID:40761744
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12320393/
Abstract

Cancer is the primary cause of death worldwide. Cancer occurrence and progression are closely associated with DNA damage repair. DNA glycosylase were the first enzymes to initiate base excision repair, and the Nei-like DNA glycosylase (NEIL) family has attracted increasing attention as an important component of DNA glycosylases. Here, we introduce the role of the NEIL family in the malignant biological behaviors of cancer, including cell proliferation, chemoradiotherapy resistance, invasion and migration, apoptosis, and stemness. Mechanisms affecting the expression of the NEIL protein family range from the transcriptional level and mRNA editing to the level of post-translational modification. Additionally, we emphasize the different functions of the NEIL family in various malignancies and present useful information that supports the hypothesis that the NEIL family could be a potential target in the treatment and diagnosis of various cancers.

摘要

癌症是全球主要的死亡原因。癌症的发生和发展与DNA损伤修复密切相关。DNA糖基化酶是启动碱基切除修复的首批酶,而类Nei DNA糖基化酶(NEIL)家族作为DNA糖基化酶的重要组成部分,已引起越来越多的关注。在此,我们介绍NEIL家族在癌症恶性生物学行为中的作用,包括细胞增殖、放化疗耐药性、侵袭和迁移、凋亡以及干性。影响NEIL蛋白家族表达的机制从转录水平、mRNA编辑到翻译后修饰水平不等。此外,我们强调了NEIL家族在各种恶性肿瘤中的不同功能,并提供了有用的信息,支持NEIL家族可能成为各种癌症治疗和诊断潜在靶点这一假说。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c04/12320393/d7a914ca6977/fcell-13-1612329-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c04/12320393/f337386655d9/fcell-13-1612329-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c04/12320393/d7a914ca6977/fcell-13-1612329-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c04/12320393/f337386655d9/fcell-13-1612329-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c04/12320393/d7a914ca6977/fcell-13-1612329-g002.jpg

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本文引用的文献

[1]
Structural and biochemical insights into NEIL2's preference for abasic sites.

Nucleic Acids Res. 2023-12-11

[2]
DNA damage repair-related gene signature for identifying the immune status and predicting the prognosis of hepatocellular carcinoma.

Sci Rep. 2023-11-3

[3]
Base Excision Repair: Mechanisms and Impact in Biology, Disease, and Medicine.

Int J Mol Sci. 2023-9-16

[4]
Cancer chemotherapy resistance: Mechanisms and recent breakthrough in targeted drug delivery.

Eur J Pharmacol. 2023-11-5

[5]
Using Affinity Pulldown Assays to Study Protein-Protein Interactions of Human NEIL1 Glycosylase and the Checkpoint Protein RAD9-RAD1-HUS1 (9-1-1) Complex.

Methods Mol Biol. 2023

[6]
Functional analyses of single nucleotide polymorphic variants of the DNA glycosylase NEIL1 in sub-Saharan African populations.

DNA Repair (Amst). 2023-9

[7]
Determination of the effects of fusaric acid, a mycotoxin, on cytotoxicity, gamma-H2AX, 8-hydroxy-2 deoxyguanosine and DNA repair gene expressions in pancreatic cancer cells.

Toxicon. 2023-8-1

[8]
Functional roles and cancer variants of the bifunctional glycosylase NEIL2.

Environ Mol Mutagen. 2024-4

[9]
The Curcumin Analog PAC Is a Potential Solution for the Treatment of Triple-Negative Breast Cancer by Modulating the Gene Expression of DNA Repair Pathways.

Int J Mol Sci. 2023-6-2

[10]
Transcriptional factor MAZ promotes cisplatin-induced DNA damage repair in lung adenocarcinoma by regulating NEIL3.

Pulm Pharmacol Ther. 2023-6

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