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急性髓系白血病患者新鲜原始细胞中P-糖蛋白表达与体外药物敏感性的比较。

Comparison of P-glycoprotein expression with in vitro drug sensitivity in fresh blast cells from acute myeloid leukaemia patients.

作者信息

Faulkner Pulsford J F, Sargent J M, Elgie A W, Williamson C J, Taylor C G

机构信息

Department of Haematology, Pembury Hospital, Kent, England, UK.

出版信息

Br J Biomed Sci. 1995 Sep;52(3):188-94.

PMID:8527996
Abstract

Anthracyclines and etoposide have been implicated in the multi-drug resistance phenotype. The mdr 1 gene encodes for the transmembrane protein P-glycoprotein. P-glycoprotein expression was measured in the fresh blast cells from 19 patients with acute myeloid leukemia using three monoclonal antibodies, C219, JSB-1 and MRK 16, and immunocytochemistry with the enzyme alkaline phosphatase as marker. Drug resistance can be identified in vitro using the predictive chemosensitivity test, the MTT (3-4,5-dimethylthiazol-2,5-diphenyl tetrazolium bromide) assay. In order to assess cell viability after drug exposure, this technique utilises the ability of cellular dehydrogenase enzymes to reduce the tetrazolium salt MTT to formazan. In vitro resistance to multi-drug resistance related cytotoxic agents was identified in the blast cells from these patients. This study showed no correlation between the results of the MTT assay and P-glycoprotein expression in this disease, suggesting either that more sensitive techniques are required to measure P-glycoprotein expression or that other drug resistance mechanisms may be involved.

摘要

蒽环类药物和依托泊苷与多药耐药表型有关。多药耐药基因1编码跨膜蛋白P-糖蛋白。使用三种单克隆抗体C219、JSB-1和MRK 16以及以碱性磷酸酶为标记物的免疫细胞化学方法,对19例急性髓性白血病患者新鲜的原始细胞中的P-糖蛋白表达进行了检测。耐药性可通过预测性化学敏感性试验即MTT(3-(4,5-二甲基噻唑-2)-2,5-二苯基四氮唑溴盐)法在体外进行鉴定。为了评估药物暴露后的细胞活力,该技术利用细胞脱氢酶将四氮唑盐MTT还原为甲臜的能力。在这些患者的原始细胞中鉴定出了对多药耐药相关细胞毒性药物的体外耐药性。这项研究表明,在该疾病中MTT试验结果与P-糖蛋白表达之间没有相关性,这表明要么需要更灵敏的技术来检测P-糖蛋白表达,要么可能涉及其他耐药机制。

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