Suppr超能文献

使用耐药基因的基因治疗。

Gene therapy with drug resistance genes.

作者信息

Zaboikin M, Srinivasakumar N, Schuening F

机构信息

Division of Hematology/Oncology, Department of Medicine, Vanderbilt University, Nashville, TN 37232, USA.

出版信息

Cancer Gene Ther. 2006 Apr;13(4):335-45. doi: 10.1038/sj.cgt.7700912.

Abstract

A major side effect of cancer chemotherapy is myelosuppression. Expression of drug-resistance genes in hematopoietic stem cells (HSC) using gene transfer methodologies holds the promise of overcoming marrow toxicity in cancer chemotherapy. Adequate protection of marrow cells in cancer patients from myelotoxicity in this way would permit the use of escalating doses of chemotherapy for eradicating residual disease. A second use of drug-resistance genes is for coexpression with a therapeutic gene in HSCs to provide a selection advantage to gene-modified cells. In this review, we discuss several drug resistance genes, which are well suited for in vivo selection as well as other newer candidate genes with potential for use in this manner.

摘要

癌症化疗的一个主要副作用是骨髓抑制。利用基因转移方法在造血干细胞(HSC)中表达耐药基因有望克服癌症化疗中的骨髓毒性。通过这种方式充分保护癌症患者的骨髓细胞免受骨髓毒性,将允许使用递增剂量的化疗来根除残留疾病。耐药基因的第二个用途是与治疗性基因在造血干细胞中共表达,为基因修饰细胞提供选择优势。在这篇综述中,我们讨论了几种非常适合体内选择的耐药基因以及其他有潜力以这种方式使用的新候选基因。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验