梭菌孢子作为癌症基因治疗的活 "特洛伊木马 "载体:与病毒递送系统的比较。

Ming Q Wei, Ruimei Ren, David Good, Jozef Anné
{"title":"梭菌孢子作为癌症基因治疗的活 \"特洛伊木马 \"载体:与病毒递送系统的比较。","authors":"Ming Q Wei, Ruimei Ren, David Good, Jozef Anné","doi":"10.1186/1479-0556-6-8","DOIUrl":null,"url":null,"abstract":"<p><p>Solid tumours account for 90% of all cancers. Gene therapy represents a potential new modality for their treatment. Up to now, several approaches have been developed, but the most efficient ones are the viral vector based gene therapy systems. However, viral vectors suffer from several deficiencies: firstly most vectors currently in use require intratumoural injection to elicit an effect. This is far from ideal as many tumours are inaccessible and many may have already spread to other parts of the body, making them difficult to locate and inject gene therapy vectors into. Second, because of cell heterogeneity within a given cancer, the vectors do not efficiently enter and kill every cancer cell. Third, hypoxia, a prevalent characteristic feature of most solid tumours, reduces the ability of the viral vectors to function and decreases viral gene expression and production. Consequently, a proportion of the tumour is left unaffected, from which tumour regrowth occurs. Thus, cancer gene therapy has yet to realise its full potential. The facultative or obligate anaerobic bacteria have been shown to selectively colonise and regerminate in solid tumours when delivered systemically. Among them, the clostridial spores were easy to produce, stable to store and safe to use as well as having extensive oncolytic ability. However, research in animals and humans has shown that oncolysis was almost always interrupted sharply at the outer rim of the viable tumour tissue where the blood supply was sufficient. These clostridial spores, though, could serve as \"Trojan horse\" for cancer gene therapy. Indeed, various spores harbouring genes for cancerstatic factors, prodrug enzymes, or proteins or cytokines had endowed with additional tumour-killing capability. Furthermore, combination of these \"Trojan horses\" with conventional chemotherapy or radiation therapies often significantly perform better, resulting in the \"cure\" of solid tumours in a high percentage of animals. It is, thus, not too difficult to predict the potential outcomes for the use of clostridial spores as \"Trojan horse\" vectors for oncolytic therapy when compared with viral vector-mediated cancer therapy for it be replication-deficient or competent. However, to move the \"Trojan horse\" to a clinic, though, additional requirements need to be satisfied (i) target tumours only and not anywhere else, and (ii) be able to completely kill primary tumours as well as metastases. Current technologies are in place to achieve these goals.</p>","PeriodicalId":12596,"journal":{"name":"Genetic Vaccines and Therapy","volume":"6 ","pages":"8"},"PeriodicalIF":0.0000,"publicationDate":"2008-02-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2267465/pdf/","citationCount":"0","resultStr":"{\"title\":\"Clostridial spores as live 'Trojan horse' vectors for cancer gene therapy: comparison with viral delivery systems.\",\"authors\":\"Ming Q Wei, Ruimei Ren, David Good, Jozef Anné\",\"doi\":\"10.1186/1479-0556-6-8\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Solid tumours account for 90% of all cancers. Gene therapy represents a potential new modality for their treatment. Up to now, several approaches have been developed, but the most efficient ones are the viral vector based gene therapy systems. However, viral vectors suffer from several deficiencies: firstly most vectors currently in use require intratumoural injection to elicit an effect. This is far from ideal as many tumours are inaccessible and many may have already spread to other parts of the body, making them difficult to locate and inject gene therapy vectors into. Second, because of cell heterogeneity within a given cancer, the vectors do not efficiently enter and kill every cancer cell. Third, hypoxia, a prevalent characteristic feature of most solid tumours, reduces the ability of the viral vectors to function and decreases viral gene expression and production. Consequently, a proportion of the tumour is left unaffected, from which tumour regrowth occurs. Thus, cancer gene therapy has yet to realise its full potential. The facultative or obligate anaerobic bacteria have been shown to selectively colonise and regerminate in solid tumours when delivered systemically. Among them, the clostridial spores were easy to produce, stable to store and safe to use as well as having extensive oncolytic ability. However, research in animals and humans has shown that oncolysis was almost always interrupted sharply at the outer rim of the viable tumour tissue where the blood supply was sufficient. These clostridial spores, though, could serve as \\\"Trojan horse\\\" for cancer gene therapy. Indeed, various spores harbouring genes for cancerstatic factors, prodrug enzymes, or proteins or cytokines had endowed with additional tumour-killing capability. Furthermore, combination of these \\\"Trojan horses\\\" with conventional chemotherapy or radiation therapies often significantly perform better, resulting in the \\\"cure\\\" of solid tumours in a high percentage of animals. It is, thus, not too difficult to predict the potential outcomes for the use of clostridial spores as \\\"Trojan horse\\\" vectors for oncolytic therapy when compared with viral vector-mediated cancer therapy for it be replication-deficient or competent. However, to move the \\\"Trojan horse\\\" to a clinic, though, additional requirements need to be satisfied (i) target tumours only and not anywhere else, and (ii) be able to completely kill primary tumours as well as metastases. Current technologies are in place to achieve these goals.</p>\",\"PeriodicalId\":12596,\"journal\":{\"name\":\"Genetic Vaccines and Therapy\",\"volume\":\"6 \",\"pages\":\"8\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2008-02-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2267465/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Genetic Vaccines and Therapy\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1186/1479-0556-6-8\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Genetic Vaccines and Therapy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1186/1479-0556-6-8","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

实体瘤占所有癌症的 90%。基因疗法是治疗实体瘤的一种潜在新方法。迄今为止,已开发出多种方法,但最有效的是基于病毒载体的基因治疗系统。然而,病毒载体有几个不足之处:首先,目前使用的大多数载体需要在肿瘤内注射才能产生效果。这并不理想,因为许多肿瘤无法进入,而且许多肿瘤可能已经扩散到身体的其他部位,因此很难定位和注射基因治疗载体。其次,由于特定癌症的细胞具有异质性,载体无法有效进入并杀死每一个癌细胞。第三,缺氧是大多数实体瘤的普遍特征,它会降低病毒载体的功能,减少病毒基因的表达和产生。因此,一部分肿瘤不受影响,肿瘤由此重新生长。因此,癌症基因疗法尚未充分发挥其潜力。事实证明,兼性或兼性厌氧细菌经全身给药后,可选择性地在实体瘤中定植和再生。其中,梭菌孢子易于生产、储存稳定、使用安全,并具有广泛的溶瘤能力。然而,在动物和人类身上进行的研究表明,溶瘤作用几乎总是在血液供应充足的有活力肿瘤组织外缘急剧中断。不过,这些梭菌孢子可以作为癌症基因治疗的 "特洛伊木马"。事实上,含有抗癌因子、原药酶、蛋白质或细胞因子基因的各种孢子都具有额外的杀灭肿瘤能力。此外,将这些 "特洛伊木马 "与传统的化疗或放射疗法结合使用,往往效果更佳,从而 "治愈 "了很高比例的动物实体瘤。因此,与病毒载体介导的癌症疗法相比,使用梭菌孢子作为 "特洛伊木马 "载体进行溶瘤疗法的潜在结果并不难预测,因为病毒载体可以是复制缺陷型的,也可以是能力型的。不过,要将 "特洛伊木马 "推向临床,还需要满足以下额外要求:(i) 只针对肿瘤,而不针对其他部位;(ii) 能够完全杀死原发肿瘤和转移瘤。目前已有技术可以实现这些目标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Clostridial spores as live 'Trojan horse' vectors for cancer gene therapy: comparison with viral delivery systems.

Solid tumours account for 90% of all cancers. Gene therapy represents a potential new modality for their treatment. Up to now, several approaches have been developed, but the most efficient ones are the viral vector based gene therapy systems. However, viral vectors suffer from several deficiencies: firstly most vectors currently in use require intratumoural injection to elicit an effect. This is far from ideal as many tumours are inaccessible and many may have already spread to other parts of the body, making them difficult to locate and inject gene therapy vectors into. Second, because of cell heterogeneity within a given cancer, the vectors do not efficiently enter and kill every cancer cell. Third, hypoxia, a prevalent characteristic feature of most solid tumours, reduces the ability of the viral vectors to function and decreases viral gene expression and production. Consequently, a proportion of the tumour is left unaffected, from which tumour regrowth occurs. Thus, cancer gene therapy has yet to realise its full potential. The facultative or obligate anaerobic bacteria have been shown to selectively colonise and regerminate in solid tumours when delivered systemically. Among them, the clostridial spores were easy to produce, stable to store and safe to use as well as having extensive oncolytic ability. However, research in animals and humans has shown that oncolysis was almost always interrupted sharply at the outer rim of the viable tumour tissue where the blood supply was sufficient. These clostridial spores, though, could serve as "Trojan horse" for cancer gene therapy. Indeed, various spores harbouring genes for cancerstatic factors, prodrug enzymes, or proteins or cytokines had endowed with additional tumour-killing capability. Furthermore, combination of these "Trojan horses" with conventional chemotherapy or radiation therapies often significantly perform better, resulting in the "cure" of solid tumours in a high percentage of animals. It is, thus, not too difficult to predict the potential outcomes for the use of clostridial spores as "Trojan horse" vectors for oncolytic therapy when compared with viral vector-mediated cancer therapy for it be replication-deficient or competent. However, to move the "Trojan horse" to a clinic, though, additional requirements need to be satisfied (i) target tumours only and not anywhere else, and (ii) be able to completely kill primary tumours as well as metastases. Current technologies are in place to achieve these goals.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Retraction: Structure based sequence analysis & epitope prediction of gp41 HIV1 envelope glycoprotein isolated in Pakistan. DNA vaccination for prostate cancer, from preclinical to clinical trials - where we stand? Evaluation of the immune responses induced by four targeted DNA vaccines encoding the juvenile liver fluke antigen, cathepsin B in a mouse model. Targeting wild-type Erythrocyte receptors for Plasmodium falciparum and vivax Merozoites by Zinc Finger Nucleases In- silico: Towards a Genetic Vaccine against Malaria. A brief review on dengue molecular virology, diagnosis, treatment and prevalence in Pakistan.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1