van der Meulen N, Prindull G, Lipp K, Winge J F
Klin Wochenschr. 1980 Jun 16;58(12):639-41. doi: 10.1007/BF01477840.
A very high degree of specific dexamethasone binding to chromatin and a marked in vitro inhibition of RNA-synthesizing capacity of purified lymphoma cell nuclei was found to correlate closely with the very strong cytolethal effect of glucocorticoids on lymphoma cells (in this case neither B- nor T-cells) of a young patient, whose condition rapidly and unexpectedly deteriorated after a total dose fo 90 mg of Prednisone given during a two day period; and in spite of prophylactic antihyperuricaemia treatment, the patient subsequently died. In this case the amount of glucocorticoid bound specifically by lymphoma chromatin was about 400% larger than is normally found in chromatin isolated from normal human thymus cells in persons on this age. The in vitro inhibition of RNA-Synthesizing activity measured with the aggregate enzyme and with isolated nuclei from lymphoma cell-nuclei by dexamethasone correlates closely to the specific dexamethasone binding capacity of chromatin. Thus a better prediction of the therapeutic effect of such lymphosarcoma cells to glucocorticoid may be possible.
发现高度特异性的地塞米松与染色质结合以及纯化的淋巴瘤细胞核的RNA合成能力在体外受到显著抑制,这与糖皮质激素对一名年轻患者的淋巴瘤细胞(在这种情况下既不是B细胞也不是T细胞)具有非常强的细胞致死作用密切相关。该患者在两天内接受了总量为90毫克的泼尼松治疗后,病情迅速且意外地恶化;尽管进行了预防性抗高尿酸血症治疗,患者随后还是死亡了。在这种情况下,淋巴瘤染色质特异性结合的糖皮质激素量比这个年龄段正常人胸腺细胞分离出的染色质中通常发现的量大约多400%。用地塞米松对聚合酶和淋巴瘤细胞核分离出的细胞核进行体外RNA合成活性抑制的测量,与染色质的地塞米松特异性结合能力密切相关。因此,对于此类淋巴瘤细胞对糖皮质激素的治疗效果可能可以做出更好的预测。