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单纯疱疹病毒溶瘤疗法用于儿童恶性肿瘤治疗

Herpes simplex virus oncolytic therapy for pediatric malignancies.

作者信息

Friedman Gregory K, Pressey Joseph G, Reddy Alyssa T, Markert James M, Gillespie G Yancey

机构信息

Department of Pediatrics, Children's Hospital of Alabama, University of Alabama at Birmingham, USA.

出版信息

Mol Ther. 2009 Jul;17(7):1125-35. doi: 10.1038/mt.2009.73. Epub 2009 Apr 14.

DOI:10.1038/mt.2009.73
PMID:19367259
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2835221/
Abstract

Despite improving survival rates for children with cancer, a subset of patients exist with disease resistant to traditional therapies such as surgery, chemotherapy, and radiation. These patients require newer, targeted treatments used alone or in combination with more traditional approaches. Oncolytic herpes simplex virus (HSV) is one of these newer therapies that offer promise for several difficult to treat pediatric malignancies. The potential benefit of HSV therapy in pediatric solid tumors including brain tumors, neuroblastomas, and sarcomas is reviewed along with the many challenges that need to be addressed prior to moving oncolytic HSV therapy from the laboratory to the beside in the pediatric population.

摘要

尽管儿童癌症患者的生存率有所提高,但仍有一部分患者的疾病对手术、化疗和放疗等传统疗法具有抗性。这些患者需要更新的靶向治疗,可单独使用或与更传统的方法联合使用。溶瘤单纯疱疹病毒(HSV)就是这些新疗法之一,有望用于治疗几种难治的儿科恶性肿瘤。本文综述了HSV疗法在包括脑肿瘤、神经母细胞瘤和肉瘤在内的儿科实体瘤中的潜在益处,以及在将溶瘤HSV疗法从实验室应用于儿科患者床边之前需要解决的诸多挑战。

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本文引用的文献

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Neuroblastoma cell lines contain pluripotent tumor initiating cells that are susceptible to a targeted oncolytic virus.神经母细胞瘤细胞系包含对靶向溶瘤病毒敏感的多能肿瘤起始细胞。
PLoS One. 2009;4(1):e4235. doi: 10.1371/journal.pone.0004235. Epub 2009 Jan 21.
2
Phase Ib trial of mutant herpes simplex virus G207 inoculated pre-and post-tumor resection for recurrent GBM.复发性胶质母细胞瘤患者在肿瘤切除前后接种突变型单纯疱疹病毒G207的Ib期试验。
Mol Ther. 2009 Jan;17(1):199-207. doi: 10.1038/mt.2008.228. Epub 2008 Oct 28.
3
The prognostic value of nestin expression in newly diagnosed glioblastoma: report from the Radiation Therapy Oncology Group.巢蛋白表达在新诊断胶质母细胞瘤中的预后价值:放射治疗肿瘤学组报告
Radiat Oncol. 2008 Sep 25;3:32. doi: 10.1186/1748-717X-3-32.
4
Histone deacetylase inhibitors augment antitumor efficacy of herpes-based oncolytic viruses.组蛋白去乙酰化酶抑制剂增强基于疱疹病毒的溶瘤病毒的抗肿瘤疗效。
Mol Ther. 2008 Sep;16(9):1546-55. doi: 10.1038/mt.2008.155. Epub 2008 Jul 22.
5
Pediatric central nervous system germ cell tumors: a review.小儿中枢神经系统生殖细胞肿瘤:综述
Oncologist. 2008 Jun;13(6):690-9. doi: 10.1634/theoncologist.2008-0037.
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Clin Cancer Res. 2008 Jun 15;14(12):3933-41. doi: 10.1158/1078-0432.CCR-07-4732.
7
Oncolytic HSV-1 infection of tumors induces angiogenesis and upregulates CYR61.肿瘤的溶瘤性单纯疱疹病毒1型感染可诱导血管生成并上调CYR61。
Mol Ther. 2008 Aug;16(8):1382-91. doi: 10.1038/mt.2008.112. Epub 2008 Jun 10.
8
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J Pediatr Hematol Oncol. 2008 Jun;30(6):425-30. doi: 10.1097/MPH.0b013e31816e22f3.
9
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10
Disease control intervals in high-risk neuroblastoma.高危神经母细胞瘤的疾病控制间隔
Cancer. 2008 Jun 15;112(12):2796-801. doi: 10.1002/cncr.23507.