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一种针对烟酰胺腺嘌呤二核苷酸磷酸(NAD(P)H):醌氧化还原酶1(NQO1)的个体化癌症化疗模型。

A Model for NAD(P)H:Quinoneoxidoreductase 1 (NQO1) Targeted Individualized Cancer Chemotherapy.

作者信息

Begleiter Asher, El-Gabalawy Nadia, Lange Laurie, Leith Marsha K, Guziec Lynn J, Guziec Frank S

机构信息

Manitoba Institute of Cell Biology, CancerCare Manitoba, Departments of Internal Medicine and Pharmacology and Therapeutics, University of Manitoba, 675 McDermot Avenue, Winnipeg, Manitoba R3E 0V9 Canada.

出版信息

Drug Target Insights. 2009;4:1-8. doi: 10.4137/dti.s1146. Epub 2009 Jan 15.

Abstract

NQO1 (NAD(P)H:quinoneoxidoreductase 1) is a reductive enzyme that is an important activator of bioreductive antitumor agents. NQO1 activity varies in individual tumors but is generally higher in tumor cells than in normal cells. NQO1 has been used as a target for tumor specific drug development. We investigated a series of bioreductive benzoquinone mustard analogs as a model for NQO1 targeted individualized cancer chemotherapy. We compared the tumor cell growth inhibitory activity of benzoquinone mustard analogs with sterically bulky groups of different size and placed at different positions on the benzoquinone ring, using tumor cell lines with different levels of NQO1. We demonstrated that functional groups of different steric size could be used to produce a series of bioreductive antitumor agents that were activated by different levels of NQO1 in tumor cells. This series of drugs could then be used to target cells with specific levels of NQO1 for growth inhibition and to avoid damage to normal cells, like bone marrow cells, that have low levels of NQO1. This approach could be used to develop new bioreductive antitumor agents for NQO1 targeted individualized cancer chemotherapy.

摘要

NQO1(NAD(P)H:醌氧化还原酶1)是一种还原酶,是生物还原抗肿瘤药物的重要激活剂。NQO1活性在个体肿瘤中有所不同,但通常在肿瘤细胞中比在正常细胞中更高。NQO1已被用作肿瘤特异性药物开发的靶点。我们研究了一系列生物还原苯醌氮芥类似物,作为NQO1靶向个体化癌症化疗的模型。我们使用具有不同NQO1水平的肿瘤细胞系,比较了苯醌氮芥类似物在苯醌环上不同位置带有不同大小空间位阻基团时的肿瘤细胞生长抑制活性。我们证明,不同空间大小的官能团可用于制备一系列生物还原抗肿瘤药物,这些药物在肿瘤细胞中被不同水平的NQO1激活。然后,这一系列药物可用于靶向具有特定NQO1水平的细胞以抑制其生长,并避免对骨髓细胞等NQO1水平较低的正常细胞造成损伤。这种方法可用于开发用于NQO1靶向个体化癌症化疗的新型生物还原抗肿瘤药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd1e/3086316/929598c0e2eb/dti-2009-001f1.jpg

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