Suppr超能文献

康普瑞他汀A-4前药对一组人恶性B淋巴细胞系的作用。

Effects of combretastatin A-4 prodrug against a panel of malignant human B-lymphoid cell lines.

作者信息

Nabha S M, Wall N R, Mohammad R M, Pettit G R, Al-Katib A M

机构信息

Division of Hematology and Oncology, Karmanos Cancer Institute, School of Medicine, Wayne State University, Detroit, Ml 48201, USA.

出版信息

Anticancer Drugs. 2000 Jun;11(5):385-92. doi: 10.1097/00001813-200006000-00009.

Abstract

Combretastatin A-4 (CA-4) is one of a family of compounds isolated from the South African willow tree Combretum caffrum. CA-4 was found to be active against murine melanoma and a variety of other human solid tumors. For the first time, we report the effect of CA-4 against a panel of malignant human B-lymphoid cell lines [early pre-B acute lymphoblastic leukemia (Reh), diffuse large cell lymphoma (WSU-DLCL2), chronic lymphocytic leukemia (WSU-CLL) and Waldenstrom's macroglobulinemia (WSU-WM)]. Our results indicate, using the prodrug form of CA-4, a concentration-dependent growth inhibition in all tested cell lines, although WSU-DLCL2 was more sensitive. Exposure to 4 nM CA-4 for 96 h induced 77% growth inhibition in Reh, 86% in WSU-CLL and 92% in WSU-WM. When used against the WSU-DLCL2 cell line, this same concentration of CA-4 was completely toxic. Morphological examination showed CA-4 induced the formation of giant, multinucleated cells, a phenomenon commonly found in mitotic catastrophe. Only minimal numbers of cells showing characteristics of apoptosis were detected. In WSU-DLCL2 cells, CA-4 (3 nM) induced the highest apoptosis (5%) after 48 h, while the percentage of dead cells was approximately 47%. Exposure of Reh, WSU-CLL, WSU-WM and WSU-DLCL2 cells for 24 h to 5 nM CA-4 induced 19, 28, 57 and 75% G2/M arrest, as determined by flow cytometry, respectively. Based on these preliminary studies, we believe that mitotic catastrophe is the predominant mechanism by which CA-4 induces cell death rather than apoptosis. Further studies to elucidate the mechanisms of CA-4 activity in vitro and in vivo are currently under investigation in our laboratory.

摘要

康普瑞他汀A - 4(CA - 4)是从南非柳树Combretum caffrum中分离出的一类化合物中的一种。人们发现CA - 4对小鼠黑色素瘤及多种其他人类实体瘤具有活性。我们首次报道了CA - 4对一组恶性人类B淋巴细胞系[早期前B急性淋巴细胞白血病(Reh)、弥漫大细胞淋巴瘤(WSU - DLCL2)、慢性淋巴细胞白血病(WSU - CLL)和华氏巨球蛋白血症(WSU - WM)]的作用。我们的结果表明,使用CA - 4的前药形式,在所有测试细胞系中均有浓度依赖性生长抑制,尽管WSU - DLCL2更敏感。暴露于4 nM CA - 4 96小时,在Reh细胞中诱导77%的生长抑制,在WSU - CLL细胞中诱导86%的生长抑制,在WSU - WM细胞中诱导92%的生长抑制。当用于WSU - DLCL2细胞系时,相同浓度的CA - 4具有完全毒性。形态学检查显示CA - 4诱导形成巨大的多核细胞,这是有丝分裂灾难中常见的现象。仅检测到极少量显示凋亡特征的细胞。在WSU - DLCL2细胞中,CA - 4(3 nM)在48小时后诱导最高凋亡率(5%),而死亡细胞百分比约为47%。通过流式细胞术测定,将Reh、WSU - CLL、WSU - WM和WSU - DLCL2细胞暴露于5 nM CA - 4 24小时,分别诱导19%、28%、57%和75%的G2/M期阻滞。基于这些初步研究,我们认为有丝分裂灾难是CA - 4诱导细胞死亡的主要机制,而非凋亡。我们实验室目前正在进行进一步研究以阐明CA - 4在体外和体内的活性机制。

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