• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

ZDHHC家族介导的S-棕榈酰化修饰在胶质母细胞瘤中的研究进展

Research progress on S-palmitoylation modification mediated by the ZDHHC family in glioblastoma.

作者信息

Tang Beiyan, Kang Wei, Dong Qiang, Qin Zhenwei, Duan Lei, Zhao Xianjun, Yuan Guoqiang, Pan Yawen

机构信息

The Second Medical College of Lanzhou University, Lanzhou, Gansu, China.

Department of Neurosurgery, Second Hospital of Lanzhou University, Lanzhou, Gansu, China.

出版信息

Front Cell Dev Biol. 2024 Nov 5;12:1413708. doi: 10.3389/fcell.2024.1413708. eCollection 2024.

DOI:10.3389/fcell.2024.1413708
PMID:39563863
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11573772/
Abstract

S-Palmitoylation has been widely noticed and studied in a variety of diseases. Increasing evidence suggests that S-palmitoylation modification also plays a key role in Glioblastoma (GBM). The zDHHC family, as an important member of S-palmitoyltransferases, has received extensive attention for its function and mechanism in GBM which is one of the most common primary malignant tumors of the brain and has an adverse prognosis. This review focuses on the zDHHC family, essential S-palmitoyltransferases, and their involvement in GBM. By summarizing recent studies on zDHHC molecules in GBM, we highlight their significance in regulating critical processes such as cell proliferation, invasion, and apoptosis. Specifically, members of zDHHC3, zDHHC4, zDHHC5 and others affect key processes such as signal transduction and phenotypic transformation in GBM cells through different pathways, which in turn influence tumorigenesis and progression. This review systematically outlines the mechanism of zDHHC family-mediated S-palmitoylation modification in GBM, emphasizes its importance in the development of this disease, and provides potential targets and strategies for the treatment of GBM. It also offers theoretical foundations and insights for future research and clinical applications.

摘要

S-棕榈酰化已在多种疾病中受到广泛关注和研究。越来越多的证据表明,S-棕榈酰化修饰在胶质母细胞瘤(GBM)中也起着关键作用。zDHHC家族作为S-棕榈酰转移酶的重要成员,因其在GBM中的功能和机制而受到广泛关注,GBM是最常见的原发性脑恶性肿瘤之一,预后不良。本综述聚焦于zDHHC家族,即重要的S-棕榈酰转移酶,及其在GBM中的作用。通过总结近期关于GBM中zDHHC分子的研究,我们强调了它们在调节细胞增殖、侵袭和凋亡等关键过程中的重要性。具体而言,zDHHC3、zDHHC4、zDHHC5等成员通过不同途径影响GBM细胞中的信号转导和表型转化等关键过程,进而影响肿瘤发生和进展。本综述系统地概述了zDHHC家族介导的GBM中S-棕榈酰化修饰的机制,强调了其在该疾病发展中的重要性,并为GBM的治疗提供了潜在靶点和策略。它还为未来的研究和临床应用提供了理论基础和见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6c5/11573772/68201213d2ad/fcell-12-1413708-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6c5/11573772/fe96a031030c/fcell-12-1413708-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6c5/11573772/15536c6fe28c/fcell-12-1413708-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6c5/11573772/68201213d2ad/fcell-12-1413708-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6c5/11573772/fe96a031030c/fcell-12-1413708-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6c5/11573772/15536c6fe28c/fcell-12-1413708-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6c5/11573772/68201213d2ad/fcell-12-1413708-g003.jpg

相似文献

1
Research progress on S-palmitoylation modification mediated by the ZDHHC family in glioblastoma.ZDHHC家族介导的S-棕榈酰化修饰在胶质母细胞瘤中的研究进展
Front Cell Dev Biol. 2024 Nov 5;12:1413708. doi: 10.3389/fcell.2024.1413708. eCollection 2024.
2
The role of s-palmitoylation in neurological diseases: implication for zDHHC family.S-棕榈酰化在神经疾病中的作用:对zDHHC家族的影响
Front Pharmacol. 2024 Jan 16;14:1342830. doi: 10.3389/fphar.2023.1342830. eCollection 2023.
3
ZDHHC5-mediated S-palmitoylation of FAK promotes its membrane localization and epithelial-mesenchymal transition in glioma.ZDHHC5 介导的 FAK 的 S-棕榈酰化促进其在胶质瘤中的膜定位和上皮-间充质转化。
Cell Commun Signal. 2024 Jan 17;22(1):46. doi: 10.1186/s12964-023-01366-z.
4
Targeted degradation of zDHHC-PATs decreases substrate S-palmitoylation.靶向降解 zDHHC-PATs 可减少底物 S-棕榈酰化。
PLoS One. 2024 Mar 21;19(3):e0299665. doi: 10.1371/journal.pone.0299665. eCollection 2024.
5
GSK3β palmitoylation mediated by ZDHHC4 promotes tumorigenicity of glioblastoma stem cells in temozolomide-resistant glioblastoma through the EZH2-STAT3 axis.由ZDHHC4介导的GSK3β棕榈酰化通过EZH2-STAT3轴促进替莫唑胺耐药性胶质母细胞瘤中胶质母细胞瘤干细胞的致瘤性。
Oncogenesis. 2022 May 23;11(1):28. doi: 10.1038/s41389-022-00402-w.
6
Protein Palmitoylation Regulates Cell Survival by Modulating XBP1 Activity in Glioblastoma Multiforme.蛋白质棕榈酰化通过调节多形性胶质母细胞瘤中的XBP1活性来调控细胞存活。
Mol Ther Oncolytics. 2020 May 22;17:518-530. doi: 10.1016/j.omto.2020.05.007. eCollection 2020 Jun 26.
7
Palmitoylation of SARS-CoV-2 S protein is critical for S-mediated syncytia formation and virus entry.SARS-CoV-2 S 蛋白的棕榈酰化对于 S 介导的合胞体形成和病毒进入至关重要。
J Med Virol. 2022 Jan;94(1):342-348. doi: 10.1002/jmv.27339. Epub 2021 Sep 23.
8
Potential Role of S-Palmitoylation in Cancer Stem Cells of Lung Adenocarcinoma.S-棕榈酰化在肺腺癌癌症干细胞中的潜在作用
Front Cell Dev Biol. 2021 Sep 21;9:734897. doi: 10.3389/fcell.2021.734897. eCollection 2021.
9
Regulatory effects of post-translational modifications on zDHHC -acyltransferases.翻译后修饰对zDHHC酰基转移酶的调控作用。
J Biol Chem. 2020 Oct 23;295(43):14640-14652. doi: 10.1074/jbc.REV120.014717. Epub 2020 Aug 17.
10
Substrate selectivity in the zDHHC family of -acyltransferases.zDHHC 酰基转移酶家族中的底物选择性。
Biochem Soc Trans. 2017 Jun 15;45(3):751-758. doi: 10.1042/BST20160309.

引用本文的文献

1
Potential therapeutic target in oncology: Protein palmitoylation (Review).肿瘤学中的潜在治疗靶点:蛋白质棕榈酰化(综述)
Oncol Rep. 2025 Oct;54(4). doi: 10.3892/or.2025.8950. Epub 2025 Jul 19.
2
Research trends of protein palmitoylation in cancer from 2004 to 2024: a bibliometric and visualization analysis.2004年至2024年癌症中蛋白质棕榈酰化的研究趋势:文献计量与可视化分析
Front Oncol. 2025 Jun 23;15:1571870. doi: 10.3389/fonc.2025.1571870. eCollection 2025.

本文引用的文献

1
Palmitoyl transferase ZDHHC20 promotes pancreatic cancer metastasis.棕榈酰转移酶 ZDHHC20 促进胰腺癌转移。
Cell Rep. 2024 May 28;43(5):114224. doi: 10.1016/j.celrep.2024.114224. Epub 2024 May 11.
2
Protein lipidation in health and disease: molecular basis, physiological function and pathological implication.蛋白质脂质化在健康和疾病中的作用:分子基础、生理功能和病理意义。
Signal Transduct Target Ther. 2024 Mar 15;9(1):60. doi: 10.1038/s41392-024-01759-7.
3
The role of s-palmitoylation in neurological diseases: implication for zDHHC family.
S-棕榈酰化在神经疾病中的作用:对zDHHC家族的影响
Front Pharmacol. 2024 Jan 16;14:1342830. doi: 10.3389/fphar.2023.1342830. eCollection 2023.
4
ZDHHC5-mediated S-palmitoylation of FAK promotes its membrane localization and epithelial-mesenchymal transition in glioma.ZDHHC5 介导的 FAK 的 S-棕榈酰化促进其在胶质瘤中的膜定位和上皮-间充质转化。
Cell Commun Signal. 2024 Jan 17;22(1):46. doi: 10.1186/s12964-023-01366-z.
5
A palmitoyl transferase chemical-genetic system to map ZDHHC-specific S-acylation.一种棕榈酰转移酶化学遗传学系统,用于绘制 ZDHHC 特异性 S-酰化图谱。
Nat Biotechnol. 2024 Oct;42(10):1548-1558. doi: 10.1038/s41587-023-02030-0. Epub 2024 Jan 8.
6
Transgelin Promotes Glioblastoma Stem Cell Hypoxic Responses and Maintenance Through p53 Acetylation.Transgelin 通过乙酰化 p53 促进脑胶质母细胞瘤干细胞的低氧反应和维持。
Adv Sci (Weinh). 2024 Feb;11(7):e2305620. doi: 10.1002/advs.202305620. Epub 2023 Dec 12.
7
Orthogonal Enzyme-Substrate Design Strategy for Discovery of Human Protein Palmitoyltransferase Substrates.正交酶-底物设计策略用于发现人类蛋白棕榈酰转移酶底物。
J Am Chem Soc. 2023 Oct 18;145(41):22287-22292. doi: 10.1021/jacs.3c04359. Epub 2023 Sep 29.
8
MGMT methylation pattern of long-term and short-term survivors of glioblastoma reveals CpGs of the enhancer region to be of high prognostic value.胶质母细胞瘤的长期和短期幸存者的 MGMT 甲基化模式显示增强子区域的 CpG 具有高预后价值。
Acta Neuropathol Commun. 2023 Aug 28;11(1):139. doi: 10.1186/s40478-023-01622-w.
9
Molecular mechanism of palmitic acid and its derivatives in tumor progression.棕榈酸及其衍生物在肿瘤进展中的分子机制。
Front Oncol. 2023 Aug 9;13:1224125. doi: 10.3389/fonc.2023.1224125. eCollection 2023.
10
Regulation of post-translational modification of PD-L1 and advances in tumor immunotherapy.PD-L1 翻译后修饰的调控与肿瘤免疫治疗的进展。
Front Immunol. 2023 Jul 24;14:1230135. doi: 10.3389/fimmu.2023.1230135. eCollection 2023.