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昼夜节律基因Per1和Per2在体内增加胶质瘤的放射敏感性。

Circadian genes Per1 and Per2 increase radiosensitivity of glioma in vivo.

作者信息

Zhanfeng Niu, Yanhui Li, Zhou Fei, Shaocai Hao, Guangxing Li, Hechun Xia

机构信息

Department of Neurosurgery, The General Hospital of Ningxia Medical University, Yinchuan, China.

Department of Neurosurgery, The Xijing Hospital of The Fourth Miltary Medical University, Xi'an, China.

出版信息

Oncotarget. 2015 Apr 30;6(12):9951-8. doi: 10.18632/oncotarget.3179.

DOI:10.18632/oncotarget.3179
PMID:25760074
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4496409/
Abstract

Per1 and Per2 play a key role in regulating the circadian rhythm in mammals. We report here that although both genes were expressed with a circadian rhythm in glioma and normal brain tissue in rats, their expression profiles differed in the two types of tissue. In addition, high expression of Per1 and Per2 in glioma tissue was associated with increased sensitivity to x-irradiation. No such sensitizing effect was observed in normal tissue. Our results suggest that Per1 and Per2 expression may increase the efficacy of radiotherapy against glioma by promoting apoptosis.

摘要

Per1和Per2在调节哺乳动物的昼夜节律中起关键作用。我们在此报告,尽管这两个基因在大鼠的胶质瘤和正常脑组织中均以昼夜节律表达,但其在这两种组织中的表达谱有所不同。此外,胶质瘤组织中Per1和Per2的高表达与对X射线照射的敏感性增加相关。在正常组织中未观察到这种致敏作用。我们的结果表明,Per1和Per2的表达可能通过促进细胞凋亡来提高对胶质瘤放疗的疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb44/4496409/d045ba223e6d/oncotarget-06-9951-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb44/4496409/042b5bf4c670/oncotarget-06-9951-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb44/4496409/2c9bcf72ee40/oncotarget-06-9951-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb44/4496409/1c51da50788f/oncotarget-06-9951-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb44/4496409/d045ba223e6d/oncotarget-06-9951-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb44/4496409/042b5bf4c670/oncotarget-06-9951-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb44/4496409/2c9bcf72ee40/oncotarget-06-9951-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb44/4496409/1c51da50788f/oncotarget-06-9951-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb44/4496409/d045ba223e6d/oncotarget-06-9951-g004.jpg

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Functional genomics identify Birc5/survivin as a candidate gene involved in the chronotoxicity of cyclin-dependent kinase inhibitors.功能基因组学鉴定 Birc5/survivin 为细胞周期蛋白依赖性激酶抑制剂的chronotoxicity 相关候选基因。
Cell Cycle. 2014;13(6):984-91. doi: 10.4161/cc.27868. Epub 2014 Jan 21.
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BMAL1-dependent regulation of the mTOR signaling pathway delays aging.
昼夜节律调节因子PERs在氧化应激、免疫及癌症发展中的作用。
Cell Commun Signal. 2025 Jan 16;23(1):30. doi: 10.1186/s12964-025-02040-2.
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Chronobiology of the Tumor Microenvironment: Implications for Therapeutic Strategies and Circadian-Based Interventions.肿瘤微环境的时间生物学:对治疗策略和基于昼夜节律的干预措施的启示
Aging Dis. 2024 Mar 27;16(2):645-657. doi: 10.14336/AD.2024.0327.
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Molecular mechanisms of tumour development in glioblastoma: an emerging role for the circadian clock.胶质母细胞瘤中肿瘤发生的分子机制:生物钟的新作用
NPJ Precis Oncol. 2024 Feb 20;8(1):40. doi: 10.1038/s41698-024-00530-z.
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