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病毒-卟啉组合:用于有效治疗胶质母细胞瘤的光动力和溶瘤病毒疗法

Viral-Porphyrin Combo: Photodynamic and Oncolytic Viral Therapy for Potent Glioblastoma Treatment.

作者信息

Nazarenko Alina S, Shkirdova Alena O, Orlova Ekaterina A, Biryukova Yulia K, Vorovitch Mikhail F, Kolyasnikova Nadezhda M, Ishmukhametov Aydar A, Tyurin Vladimir S, Zamilatskov Ilya A

机构信息

Chumakov Federal Scientific Center for Research and Development of Immune-and-Biological Products of Russian Academy of Sciences (Institute of Poliomyelitis), 108819 Moscow, Russia.

Frumkin Institute of Physical Chemistry and Electrochemistry, Russian Academy of Sciences, 119071 Moscow, Russia.

出版信息

Int J Mol Sci. 2024 Nov 22;25(23):12578. doi: 10.3390/ijms252312578.

Abstract

Combined viral and photodynamic therapy for oncological diseases has great potential to treat aggressive tumors such as glioblastomas. A conjugate of vesicular stomatitis virus (VSV) with protoporphyrin IX was prepared, and its oncolytic effects were studied and compared to the effects of the individual components. The VSV showed an oncolytic effect on glioblastoma cell lines T98G and LN229 at a virus titer of 10 TCID/mL. A VSV titer of 10 TCID/mL was sufficient for neuroblastoma cell death. A study of the effect of VSV in tumor 3D cell modeling found that VSV had a clear viral cytopathic effect on spheroids of T98G and LN229 cells. Conjugation with the porphyrin significantly reduced the viral titer, but when irradiated, lysis of cells was observed. Photodynamic treatment of T98G and LN229 cells and spheroids with protoporphyrin IX as a photosensitizer also had a cytotoxic effect on cells and, to a lesser extent, on the tumoroids, as complete cell death was not achieved for the tumoroids. The combination therapy, which involved sequential photodynamic therapy using protoporphyrin IX as a photosensitizer and treatment with VSV, was shown to significantly enhance efficacy, resulting in complete cell death of both T98G and LN229 cells and tumoroids. The combination treatment allowed for the use of a lower viral titer (10-10 TCID/mL) and a lower porphyrin concentration (0.5 μg/mL) to achieve a significant cytotoxic effect. As a result, the implementation of this combination therapy would likely lead to fewer side effects from the treatment. This study clearly demonstrated the excellent perspectives of combination therapy for the treatment of highly aggressive tumors such as glioblastomas.

摘要

病毒与光动力联合疗法治疗肿瘤疾病在治疗侵袭性肿瘤如胶质母细胞瘤方面具有巨大潜力。制备了水泡性口炎病毒(VSV)与原卟啉IX的共轭物,并研究了其溶瘤效果,并与单个成分的效果进行了比较。VSV在病毒滴度为10 TCID/mL时对胶质母细胞瘤细胞系T98G和LN229显示出溶瘤作用。10 TCID/mL的VSV滴度足以导致神经母细胞瘤细胞死亡。在肿瘤3D细胞模型中对VSV作用的研究发现,VSV对T98G和LN229细胞的球体有明显的病毒细胞病变效应。与卟啉共轭显著降低了病毒滴度,但照射后观察到细胞裂解。以原卟啉IX作为光敏剂对T98G和LN229细胞及球体进行光动力治疗,对细胞也有细胞毒性作用,对类肿瘤细胞的作用较小,因为类肿瘤细胞未实现完全细胞死亡。以原卟啉IX作为光敏剂进行序贯光动力治疗并联合VSV治疗的联合疗法显示出显著提高疗效,导致T98G和LN229细胞及类肿瘤细胞完全死亡。联合治疗允许使用较低的病毒滴度(10 - 10 TCID/mL)和较低的卟啉浓度(0.5 μg/mL)来实现显著的细胞毒性作用。因此,实施这种联合疗法可能会减少治疗的副作用。这项研究清楚地证明了联合疗法在治疗如胶质母细胞瘤等高度侵袭性肿瘤方面的优异前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf49/11640982/55dd96ef748e/ijms-25-12578-g001.jpg

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