Zoref-Shani E, Lavie R, Bromberg Y, Beery E, Sidi Y, Sperling O, Nordenberg J
Department of Chemical Pathology, Sackler School of Medicine, Tel Aviv University, Israel.
J Cancer Res Clin Oncol. 1994;120(12):717-22. doi: 10.1007/BF01194269.
The effects of the differentiation-inducing agents sodium butyrate (NaOBt), dimethylsulfoxide (DMSO) and mycophenolic acid (MA), on purine nucleotide metabolism, was studied in an ovarian carcinoma cell line (GZL-8). Exposure to these agents inhibited cell proliferation, but did not affect cell viability. Three hours following exposure, NaOBt and DMSO moderately decelerated purine synthesis de novo, but MA accelerated it three-fold, this being associated with a two-fold increase in the excretion of hypoxanthine and xanthine into the incubation medium. NaOBt and DMSO did not affect the cellular nucleotide content, but MA caused a 73% decrease in GTP content and about a 50% increase in the cellular content of UTP. The following alterations in cellular enzyme activity were observed 72 h following exposure: NaOBt decreased the activity of hypoxanthine-guanine phosphoribosyltransferase and increased the activity of IMP and of AMP 5'-nucleotidases, DMSO increased the activity of IMP 5'-nucleotidase, and MA increased the activity of the two nucleotidases. The results suggest that, in the carcinoma cell line studied, the differentiation process induced by NaOBt and DMSO may be associated with a general shift in the direction of purine metabolism from anabolism to catabolism, whereas that induced by MA is associated with a specific decrease in the production of GTP.
在一种卵巢癌细胞系(GZL-8)中研究了分化诱导剂丁酸钠(NaOBt)、二甲基亚砜(DMSO)和霉酚酸(MA)对嘌呤核苷酸代谢的影响。暴露于这些试剂会抑制细胞增殖,但不影响细胞活力。暴露三小时后,NaOBt和DMSO适度减缓了嘌呤的从头合成,但MA使其加速了三倍,这与次黄嘌呤和黄嘌呤向孵育培养基中的排泄增加两倍有关。NaOBt和DMSO不影响细胞核苷酸含量,但MA导致GTP含量降低73%,UTP细胞含量增加约50%。暴露72小时后观察到细胞酶活性有以下变化:NaOBt降低了次黄嘌呤-鸟嘌呤磷酸核糖转移酶的活性,增加了IMP和AMP 5'-核苷酸酶的活性,DMSO增加了IMP 5'-核苷酸酶的活性,MA增加了这两种核苷酸酶的活性。结果表明,在所研究的癌细胞系中,NaOBt和DMSO诱导的分化过程可能与嘌呤代谢方向从合成代谢向分解代谢的总体转变有关,而MA诱导的分化过程与GTP产生的特异性降低有关。