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溶瘤腺病毒用于癌症基因治疗。

Cancer gene therapy with oncolytic adenoviruses.

作者信息

Guse K, Hemminki A

机构信息

Cancer Gene Therapy Group, Molecular Cancer Biology Program & Transplantation Laboratory, Haartman Institute, University of Helsinki, and HUSLAB, Helsinki University Central Hospital, Helsinki, Finland.

出版信息

J BUON. 2009 Sep;14 Suppl 1:S7-15.

Abstract

Metastatic cancer remains difficult to treat effectively and treatments are in most cases not curative despite significant side effects. Novel, targeted approaches such as gene therapy hold promise for the treatment of various tumor types. Among the most promising cancer gene therapy approaches are oncolytic adenoviruses, which are able to infect, replicate in and lyse tumor cells. Recent data from clinical trials with these vectors have shown that they are safe. However, antitumor efficacy needs to be improved to make oncolytic adenoviruses a viable treatment alternative for cancer patients. This review focuses on targeting strategies to improve tumor cell transduction and cancer cell selective replication. Strategies to improve antitumor efficacy by arming the virus with therapeutic transgenes are also discussed. Furthermore, an overview of the most important clinical approaches with oncolytic adenoviruses is given.

摘要

转移性癌症仍然难以得到有效治疗,尽管副作用严重,但大多数情况下治疗并不能治愈。诸如基因治疗等新型靶向方法有望用于治疗多种肿瘤类型。溶瘤腺病毒是最有前景的癌症基因治疗方法之一,它能够感染肿瘤细胞、在肿瘤细胞中复制并裂解肿瘤细胞。这些载体的临床试验最新数据表明它们是安全的。然而,需要提高抗肿瘤疗效,以使溶瘤腺病毒成为癌症患者可行的治疗选择。本综述重点关注改善肿瘤细胞转导和癌细胞选择性复制的靶向策略。还讨论了通过用治疗性转基因武装病毒来提高抗肿瘤疗效的策略。此外,还概述了溶瘤腺病毒最重要的临床应用方法。

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