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与VP 16 - 213孵育后造血细胞的生长

Growth of hemopoietic cells after incubation with VP 16-213.

作者信息

Schulze E, Hofmann U, Woetzel M, Helbig W

机构信息

Department of Internal Medicine, Karl-Marx-University, Leipzig, GDR.

出版信息

Folia Haematol Int Mag Klin Morphol Blutforsch. 1989;116(3-4):591-6.

PMID:2480314
Abstract

We examined the effect of various concentrations of VP 16-213 (25-125 microM/l, 2-h incubation on normal and complete remission bone marrow from patients with acute leukaemia and on leukaemic blasts. The maximal tolerated dose of the drug for normal bone marrow GM-CFC was between 75 and 100 microM/l whereas that for complete remission bone marrow was distinctly lower. More early stem cells measured by aid of LTBMC were more resistant in normal, but not in every remission bone marrow. We have to examine if these LTBMC results are influenced by a damaged microenvironment by using 2 stage LTBMC. Spontaneous leukaemic cells showed a different, sometimes lower sensitivity to VP 16-213 doses maximally tolerated by normal hemopoietic cells so that the VP 16-213 incubation must not be effective for every leukaemia.

摘要

我们研究了不同浓度的VP 16 - 213(25 - 125微摩尔/升,孵育2小时)对急性白血病患者正常及完全缓解期骨髓以及白血病原始细胞的影响。该药物对正常骨髓粒-巨噬细胞集落形成细胞(GM - CFC)的最大耐受剂量在75至100微摩尔/升之间,而对完全缓解期骨髓的最大耐受剂量则明显更低。借助长期骨髓培养(LTBMC)检测发现,更多的早期干细胞在正常骨髓中更具抗性,但在并非所有缓解期骨髓中都是如此。我们必须通过两阶段长期骨髓培养来研究这些长期骨髓培养结果是否受到受损微环境的影响。自发白血病细胞对正常造血细胞最大耐受剂量的VP 16 - 213表现出不同的敏感性,有时敏感性更低,因此VP 16 - 213孵育对每种白血病不一定都有效。

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