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苯达莫司汀与抗代谢物联合对儿童急性淋巴细胞白血病细胞的作用

The combination effects of bendamustine with antimetabolites against childhood acute lymphoblastic leukemia cells.

作者信息

Goto Shoko, Goto Hiroaki, Yokosuka Tomoko

机构信息

Division of Hemato-Oncology and Regenerative Medicine, Kanagawa Children's Medical Center, 2-138-4 Mutsukawa, Minami-ku, Yokohama, 232-8555, Japan.

出版信息

Int J Hematol. 2016 May;103(5):572-83. doi: 10.1007/s12185-016-1952-z. Epub 2016 Feb 17.

Abstract

Bendamustine combined with other drugs is clinically efficacious for some adult lymphoid malignancies, but to date there are no reports of the use of such combinatorial approaches in pediatric patients. We investigated the in vitro activity of bendamustine combined with other antimetabolite drugs on B cell precursor acute lymphoblastic leukemia (BCP-ALL) cell lines established from pediatric patients with refractory or relapsed ALL. We also developed a mathematically drown improved isobologram method to assess the data objectively. Three BCP-ALL cell lines; YCUB-2, YCUB-5, and YCUB-6, were simultaneously exposed to various concentrations of bendamustine and cladribine, cytarabine, fludarabine, or clofarabine. Cell growth inhibition was determined using the WST-8 assay. Combinatorial effects were estimated using our improved isobologram method with IC80 (drug concentration corresponding to 80 % of maximum inhibition). Bendamustine alone inhibited ALL cell growth with mean IC80 values of 11.30-18.90 μg/ml. Combinations of bendamustine with other drugs produced the following effects: (1) cladribine; synergistic-to-additive on all cell lines; (2) cytarabine; synergistic-to-additive on YCUB-5 and YCUB-6, and synergistic-to-antagonistic on YCUB-2; (3) fludarabine; additive-to-antagonistic on YCUB-5, and synergistic-to-antagonistic on YCUB-2 and YCUB-6; (4) clofarabine; additive-to-antagonistic on all cell lines. Flow cytometric analysis also showed the combination effects of bendamustine and cladribine. Bendamustine/cladribine or bendamustine/cytarabine may thus represent a promising combination for salvage treatment in childhood ALL.

摘要

苯达莫司汀与其他药物联合使用对某些成人淋巴系统恶性肿瘤具有临床疗效,但迄今为止,尚无关于在儿科患者中使用这种联合治疗方法的报道。我们研究了苯达莫司汀与其他抗代谢药物联合使用对从难治性或复发性急性淋巴细胞白血病(ALL)儿科患者中建立的B细胞前体急性淋巴细胞白血病(BCP-ALL)细胞系的体外活性。我们还开发了一种数学推导的改良等效线图法来客观评估数据。将三种BCP-ALL细胞系;YCUB-2、YCUB-5和YCUB-6同时暴露于不同浓度的苯达莫司汀和克拉屈滨、阿糖胞苷、氟达拉滨或氯法拉滨中。使用WST-8法测定细胞生长抑制情况。使用我们改良的等效线图法,以IC80(对应最大抑制80%的药物浓度)估计联合效应。单独使用苯达莫司汀可抑制ALL细胞生长,平均IC80值为11.30 - 18.90μg/ml。苯达莫司汀与其他药物联合使用产生了以下效应:(1)克拉屈滨;对所有细胞系均为协同至相加效应;(2)阿糖胞苷;对YCUB-5和YCUB-6为协同至相加效应,对YCUB-2为协同至拮抗效应;(3)氟达拉滨;对YCUB-5为相加至拮抗效应,对YCUB-2和YCUB-6为协同至拮抗效应;(4)氯法拉滨;对所有细胞系均为相加至拮抗效应。流式细胞术分析也显示了苯达莫司汀和克拉屈滨的联合效应。因此,苯达莫司汀/克拉屈滨或苯达莫司汀/阿糖胞苷可能是儿童ALL挽救治疗的一种有前景的联合方案。

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