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靶向YY1在胶质母细胞瘤中的治疗意义

Therapeutic Implications of Targeting YY1 in Glioblastoma.

作者信息

Navasardyan Inesa, Zaravinos Apostolos, Bonavida Benjamin

机构信息

College of Osteopathic Medicine of the Pacific, Western University of Health Sciences, Pomona, CA 91766, USA.

Department of Microbiology, Immunology & Molecular Genetics, University of California at Los Angeles, Los Angeles, CA 90095, USA.

出版信息

Cancers (Basel). 2024 May 30;16(11):2074. doi: 10.3390/cancers16112074.

DOI:10.3390/cancers16112074
PMID:38893192
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11171050/
Abstract

The transcription factor Yin Yang 1 (YY1) plays a pivotal role in the pathogenesis of glioblastoma multiforme (GBM), an aggressive form of brain tumor. This review systematically explores the diverse roles of YY1 overexpression and activities in GBM, including its impact on the tumor microenvironment (TME) and immune evasion mechanisms. Due to the poor response of GBM to current therapies, various findings of YY1-associated pathways in the literature provide valuable insights into novel potential targeted therapeutic strategies. Moreover, YY1 acts as a significant regulator of immune checkpoint molecules and, thus, is a candidate therapeutic target in combination with immune checkpoint inhibitors. Different therapeutic implications targeting YY1 in GBM and its inherent associated challenges encompass the use of nanoparticles, YY1 inhibitors, targeted gene therapy, and exosome-based delivery systems. Despite the inherent complexities of such methods, the successful targeting of YY1 emerges as a promising avenue for reshaping GBM treatment strategies, presenting opportunities for innovative therapeutic approaches and enhanced patient outcomes.

摘要

转录因子阴阳1(YY1)在多形性胶质母细胞瘤(GBM)(一种侵袭性脑肿瘤)的发病机制中起关键作用。本综述系统地探讨了YY1过表达和活性在GBM中的多种作用,包括其对肿瘤微环境(TME)和免疫逃逸机制的影响。由于GBM对当前治疗反应不佳,文献中关于YY1相关途径的各种研究结果为新型潜在靶向治疗策略提供了有价值的见解。此外,YY1作为免疫检查点分子的重要调节因子,因此是与免疫检查点抑制剂联合使用的候选治疗靶点。针对GBM中YY1的不同治疗意义及其固有的相关挑战包括使用纳米颗粒、YY1抑制剂、靶向基因治疗和基于外泌体的递送系统。尽管这些方法存在固有的复杂性,但成功靶向YY1成为重塑GBM治疗策略的一个有前景的途径,为创新治疗方法和改善患者预后提供了机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30c3/11171050/7812436b5e35/cancers-16-02074-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30c3/11171050/91ea380671cd/cancers-16-02074-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30c3/11171050/dc8e3ed3f2ae/cancers-16-02074-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30c3/11171050/c772b5394600/cancers-16-02074-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30c3/11171050/87302d5529c2/cancers-16-02074-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30c3/11171050/7a2aba5d6601/cancers-16-02074-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30c3/11171050/7812436b5e35/cancers-16-02074-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30c3/11171050/91ea380671cd/cancers-16-02074-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30c3/11171050/dc8e3ed3f2ae/cancers-16-02074-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30c3/11171050/c772b5394600/cancers-16-02074-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30c3/11171050/87302d5529c2/cancers-16-02074-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30c3/11171050/7a2aba5d6601/cancers-16-02074-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30c3/11171050/7812436b5e35/cancers-16-02074-g006.jpg

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本文引用的文献

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Cancers (Basel). 2024 Mar 21;16(6):1237. doi: 10.3390/cancers16061237.
2
Cross-Talks between RKIP and YY1 through a Multilevel Bioinformatics Pan-Cancer Analysis.通过多层次生物信息学泛癌分析探究RKIP与YY1之间的相互作用
Cancers (Basel). 2023 Oct 11;15(20):4932. doi: 10.3390/cancers15204932.
3
Epigenetic regulation of enhancer of zeste homolog 2 (EZH2) -Yin Yang 1 (YY1) axis in cancer.癌症中zeste同源物2(EZH2)-阴阳1(YY1)轴的表观遗传调控
Pathol Res Pract. 2023 Nov;251:154885. doi: 10.1016/j.prp.2023.154885. Epub 2023 Oct 10.
4
Role of YY1 in the Regulation of Anti-Apoptotic Gene Products in Drug-Resistant Cancer Cells.YY1在耐药癌细胞中抗凋亡基因产物调控中的作用
Cancers (Basel). 2023 Aug 25;15(17):4267. doi: 10.3390/cancers15174267.
5
AKIP1 accelerates glioblastoma progression through stabilizing EGFR expression.AKIP1 通过稳定 EGFR 表达促进胶质母细胞瘤进展。
Oncogene. 2023 Sep;42(39):2905-2918. doi: 10.1038/s41388-023-02796-2. Epub 2023 Aug 18.
6
Genetically modified IL2 bone-marrow-derived myeloid cells reprogram the glioma immunosuppressive tumor microenvironment.基因改造的白细胞介素-2骨髓来源的髓样细胞可重编程胶质瘤免疫抑制性肿瘤微环境。
Cell Rep. 2023 Aug 29;42(8):112891. doi: 10.1016/j.celrep.2023.112891. Epub 2023 Jul 28.
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Targeting Transcription Factor YY1 for Cancer Treatment: Current Strategies and Future Directions.靶向转录因子YY1用于癌症治疗:当前策略与未来方向
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