• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

使用改良的DiSC检测方法增强慢性淋巴细胞白血病的体外药敏试验

Enhanced ex vivo drug sensitivity testing of chronic lymphocytic leukaemia using refined DiSC assay methodology.

作者信息

Bosanquet A G, Bell P B

机构信息

Bath Cancer Research Unit, University of Bath, Royal United Hospital, U.K.

出版信息

Leuk Res. 1996 Feb;20(2):143-53. doi: 10.1016/0145-2126(95)00127-1.

DOI:10.1016/0145-2126(95)00127-1
PMID:8628013
Abstract

Ex vivo drug sensitivity testing is of considerable benefit in aiding the choice of optimum chemotherapy for leukaemia patients, especially when several therapeutic options exist, e.g. for relapsed chronic lymphocytic leukaemia (CLL). We have used the Differential Staining Cytotoxicity (DiSC) assay to assess drug sensitivity in CLL for over a decade and here present many methodological improvements, including depositing multiple samples per microscope slide and performing a rapid LC90 evaluation. Using these improvements, 412/450 specimens were successfully tested. Failures were mainly due to extended specimen transit time. All 38 drugs tested exhibited dose-dependent cell kill and broad ranges of resultant LC90S were observed. Comparison of 2- and 4-day incubations underscored a requirement for 4-day incubation with pentostatin and steroids. The rapid, simple and streamlined DiSC assay presented here can aid choice of optimum therapy, identify novel anticancer agents and be used to study drug resistance.

摘要

体外药敏试验对于帮助白血病患者选择最佳化疗方案具有相当大的益处,尤其是在存在多种治疗选择时,例如复发性慢性淋巴细胞白血病(CLL)。我们使用差异染色细胞毒性(DiSC)试验评估CLL的药物敏感性已有十多年,在此展示了许多方法上的改进,包括在每张显微镜载玻片上放置多个样本以及进行快速LC90评估。利用这些改进,成功检测了450个样本中的412个。失败主要是由于样本运输时间延长。所测试的所有38种药物均表现出剂量依赖性细胞杀伤作用,并且观察到了广泛的LC90结果范围。对2天和4天孵育的比较强调了喷司他丁和类固醇需要进行4天孵育。这里介绍的快速、简单且简化的DiSC试验有助于选择最佳治疗方案、识别新型抗癌药物并用于研究耐药性。

相似文献

1
Enhanced ex vivo drug sensitivity testing of chronic lymphocytic leukaemia using refined DiSC assay methodology.使用改良的DiSC检测方法增强慢性淋巴细胞白血病的体外药敏试验
Leuk Res. 1996 Feb;20(2):143-53. doi: 10.1016/0145-2126(95)00127-1.
2
Ex vivo assessment of drug response by differential staining cytotoxicity (DiSC) assay suggests a biological basis for equality of chemotherapy irrespective of age for patients with chronic lymphocytic leukaemia.通过差异染色细胞毒性(DiSC)测定法对药物反应进行的体外评估表明,慢性淋巴细胞白血病患者化疗效果不受年龄影响,存在生物学基础。
Leukemia. 2000 Apr;14(4):712-5. doi: 10.1038/sj.leu.2401727.
3
Drug cross-resistance and therapy-induced resistance in chronic lymphocytic leukaemia by an enhanced method of individualised tumour response testing.通过一种改进的个体化肿瘤反应检测方法研究慢性淋巴细胞白血病中的药物交叉耐药性和治疗诱导的耐药性。
Br J Haematol. 2009 Aug;146(4):384-95. doi: 10.1111/j.1365-2141.2009.07741.x. Epub 2009 Jun 22.
4
Novel ex vivo analysis of nonclassical, pleiotropic drug resistance and collateral sensitivity induced by therapy provides a rationale for treatment strategies in chronic lymphocytic leukemia.对治疗诱导的非经典、多效性耐药和协同敏感性进行的新型体外分析为慢性淋巴细胞白血病的治疗策略提供了理论依据。
Blood. 1996 Mar 1;87(5):1962-71.
5
Methylprednisolone in advanced chronic lymphocytic leukaemia: rationale for, and effectiveness of treatment suggested by DiSC assay.甲泼尼龙用于晚期慢性淋巴细胞白血病:Disc 检测提示的治疗原理及有效性
Acta Haematol. 1995;93(2-4):73-9. doi: 10.1159/000204115.
6
Rituximab and 17-allylamino-17-demethoxygeldanamycin induce synergistic apoptosis in B-cell chronic lymphocytic leukaemia.利妥昔单抗和17-烯丙胺基-17-去甲氧基格尔德霉素可诱导B细胞慢性淋巴细胞白血病细胞发生协同凋亡。
Br J Haematol. 2007 Dec;139(5):837-44. doi: 10.1111/j.1365-2141.2007.06878.x. Epub 2007 Oct 19.
7
Prognosis for fludarabine therapy of chronic lymphocytic leukaemia based on ex vivo drug response by DiSC assay.基于DiSC分析的体外药物反应对慢性淋巴细胞白血病氟达拉滨治疗的预后评估
Br J Haematol. 1999 Jul;106(1):71-7. doi: 10.1046/j.1365-2141.1999.01516.x.
8
Comparison of the in vitro effects of the anti-CD20 antibodies rituximab and GA101 on chronic lymphocytic leukaemia cells.比较抗 CD20 抗体利妥昔单抗和 GA101 对慢性淋巴细胞白血病细胞的体外作用。
Br J Haematol. 2011 Feb;152(3):295-306. doi: 10.1111/j.1365-2141.2010.08428.x. Epub 2010 Dec 13.
9
Actions of the selective protein kinase C inhibitor PKC412 on B-chronic lymphocytic leukemia cells in vitro.选择性蛋白激酶C抑制剂PKC412对B细胞慢性淋巴细胞白血病细胞的体外作用
Haematologica. 2002 Feb;87(2):167-76.
10
Laboratory determination of chemotherapeutic drug resistance in tumor cells from patients with leukemia, using a fluorometric microculture cytotoxicity assay (FMCA).使用荧光微量培养细胞毒性测定法(FMCA)对白血病患者肿瘤细胞中的化疗药物耐药性进行实验室测定。
Int J Cancer. 1992 Jan 21;50(2):177-85. doi: 10.1002/ijc.2910500204.

引用本文的文献

1
The first-in-Africa ex vivo drug sensitivity testing platform identifies novel drug combinations for South African leukaemia patient cohort.非洲首个离体药敏试验平台为南非白血病患者群体确定了新型药物组合。
Sci Rep. 2025 Mar 17;15(1):9160. doi: 10.1038/s41598-025-93634-w.
2
Individualized tumor response testing for prediction of response to Paclitaxel and Cisplatin chemotherapy in patients with advanced gastric cancer.个体化肿瘤反应测试预测晚期胃癌患者对紫杉醇和顺铂化疗的反应。
J Korean Med Sci. 2010 May;25(5):684-90. doi: 10.3346/jkms.2010.25.5.684. Epub 2010 Apr 21.
3
In vitro assays for the evaluation of drug resistance in tumor cells.
用于评估肿瘤细胞耐药性的体外试验。
Clin Exp Med. 2009 Mar;9(1):1-7. doi: 10.1007/s10238-008-0011-3. Epub 2008 Sep 26.
4
In B-CLL, the codon 72 polymorphic variants of p53 are not related to drug resistance and disease prognosis.在B细胞慢性淋巴细胞白血病中,p53基因第72位密码子的多态性变体与耐药性及疾病预后无关。
BMC Cancer. 2005 Aug 18;5:105. doi: 10.1186/1471-2407-5-105.
5
Determination of caspase-3 activation fails to predict chemosensitivity in primary acute myeloid leukemia blasts.半胱天冬酶-3激活的测定无法预测原发性急性髓系白血病母细胞的化疗敏感性。
BMC Cancer. 2005 Jun 11;5:60. doi: 10.1186/1471-2407-5-60.
6
Ex vivo cytotoxic drug evaluation by DiSC assay to expedite identification of clinical targets: results with 8-chloro-cAMP.通过DiSC分析进行体外细胞毒性药物评估以加速临床靶点的鉴定:8-氯-cAMP的研究结果
Br J Cancer. 1997;76(4):511-8. doi: 10.1038/bjc.1997.417.