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辐射对神经胶质瘤体外和体内侵袭与迁移的影响

Impact of Radiation on Invasion and Migration of Glioma In Vitro and In Vivo.

作者信息

Franco Marina Santiago, Raulefs Susanne, Schilling Daniela, Combs Stephanie E, Schmid Thomas E

机构信息

School of Medicine and Health, Department of Radiation Oncology, TUM University Hospital, Technical University of Munich, 81675 Munich, Germany.

Institute of Radiation Medicine, Helmholtz Munich, 85764 Neuherberg, Germany.

出版信息

Cancers (Basel). 2024 Nov 21;16(23):3900. doi: 10.3390/cancers16233900.


DOI:10.3390/cancers16233900
PMID:39682088
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11640451/
Abstract

Glioblastoma (GBM) constitutes the most common primary brain tumor and it remains incurable despite therapeutic advances. The high infiltration/invasion potential of GBM cells is considered to be one of the reasons for the inevitable recurrence of the disease. Radiotherapy (RT) is part of the standard care for patients with GBM, and its benefits on overall survival are extensively reported. However, numerous preclinical studies show that X-ray irradiation can enhance the motility of GBM cells. In the present review, we bring together state-of-the-art research on the impact of radiation on GBM cell motility. The mechanisms through which irradiation impacts the brain tumor microenvironment and the tumor cells themselves, leading to more aggressive/invasive tumors, are described. Finally, we summarize potential pharmacological strategies to overcome this problem. Clinical data validating the occurrence of these processes are urgently needed as they could be of great value for patient outcomes. With this comprehensive review, we expect to highlight the need for methods which allow for monitoring the post-irradiation invasive behavior of GBM in patients.

摘要

胶质母细胞瘤(GBM)是最常见的原发性脑肿瘤,尽管治疗取得了进展,但它仍然无法治愈。GBM细胞的高浸润/侵袭潜能被认为是该疾病不可避免复发的原因之一。放射治疗(RT)是GBM患者标准治疗的一部分,其对总生存期的益处已有广泛报道。然而,大量临床前研究表明,X射线照射可增强GBM细胞的运动能力。在本综述中,我们汇集了关于辐射对GBM细胞运动影响的最新研究。描述了辐射影响脑肿瘤微环境和肿瘤细胞本身从而导致更具侵袭性/浸润性肿瘤的机制。最后,我们总结了克服这一问题的潜在药理学策略。迫切需要验证这些过程发生的临床数据,因为它们对患者的治疗结果可能具有重要价值。通过这一全面综述,我们希望强调需要能够监测患者放疗后GBM侵袭行为的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4124/11640451/34facfd9c480/cancers-16-03900-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4124/11640451/b6ad8fbc8dab/cancers-16-03900-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4124/11640451/1562d7617280/cancers-16-03900-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4124/11640451/34facfd9c480/cancers-16-03900-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4124/11640451/b6ad8fbc8dab/cancers-16-03900-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4124/11640451/1562d7617280/cancers-16-03900-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4124/11640451/34facfd9c480/cancers-16-03900-g003.jpg

相似文献

[1]
Impact of Radiation on Invasion and Migration of Glioma In Vitro and In Vivo.

Cancers (Basel). 2024-11-21

[2]
Evaluation of radiation-related invasion in primary patient-derived glioma cells and validation with established cell lines: impact of different radiation qualities with differing LET.

J Neurooncol. 2018-6-8

[3]
Genistein inhibits radiation-induced invasion and migration of glioblastoma cells by blocking the DNA-PKcs/Akt2/Rac1 signaling pathway.

Radiother Oncol. 2021-2

[4]
Anti-invasive efficacy and survival benefit of the YAP-TEAD inhibitor verteporfin in preclinical glioblastoma models.

Neuro Oncol. 2022-5-4

[5]
Late Effects of Radiation Prime the Brain Microenvironment for Accelerated Tumor Growth.

Int J Radiat Oncol Biol Phys. 2018-8-30

[6]
Inhibition of radiation-induced glioblastoma invasion by genetic and pharmacological targeting of MDA-9/Syntenin.

Proc Natl Acad Sci U S A. 2017-1-10

[7]
Tetraspanins predict the prognosis and characterize the tumor immune microenvironment of glioblastoma.

Sci Rep. 2023-8-16

[8]
CXCR4 increases in-vivo glioma perivascular invasion, and reduces radiation induced apoptosis: A genetic knockdown study.

Oncotarget. 2016-12-13

[9]
Post-radiation increase in VEGF enhances glioma cell motility in vitro.

Radiat Oncol. 2012-2-22

[10]
MicroRNA-451 Inhibits Migration of Glioblastoma while Making It More Susceptible to Conventional Therapy.

Noncoding RNA. 2019-3-15

本文引用的文献

[1]
Secrets of DNA-PKcs beyond DNA repair.

NPJ Precis Oncol. 2024-7-23

[2]
Notch signaling pathway in cancer: from mechanistic insights to targeted therapies.

Signal Transduct Target Ther. 2024-5-27

[3]
Non-targeted effects of radiation therapy for glioblastoma.

Heliyon. 2024-5-9

[4]
Understanding the immunosuppressive microenvironment of glioma: mechanistic insights and clinical perspectives.

J Hematol Oncol. 2024-5-8

[5]
The Impact of Lateral Ventricular Opening in the Resection of Newly Diagnosed High-Grade Gliomas: A Single Center Experience.

Cancers (Basel). 2024-4-19

[6]
Mechanism of Notch Signaling Pathway in Malignant Progression of Glioblastoma and Targeted Therapy.

Biomolecules. 2024-4-15

[7]
Microenvironmental reorganization in brain tumors following radiotherapy and recurrence revealed by hyperplexed immunofluorescence imaging.

Nat Commun. 2024-4-15

[8]
Intrinsic and Microenvironmental Drivers of Glioblastoma Invasion.

Int J Mol Sci. 2024-2-22

[9]
Epidermal Growth Factor Receptor Inhibitors in Glioblastoma: Current Status and Future Possibilities.

Int J Mol Sci. 2024-2-15

[10]
Efficacy of combined tumor irradiation and K3.1-targeting with TRAM-34 in a syngeneic glioma mouse model.

Sci Rep. 2023-11-23

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