Fibach E, Gambari R, Shaw P A, Maniatis G, Reuben R C, Sassa S, Rifkind R A, Marks P A
Proc Natl Acad Sci U S A. 1979 Apr;76(4):1906-10. doi: 10.1073/pnas.76.4.1906.
Previous studies demonstrated that 12-O-tetradecanoyl-phorbol-13-acetate (TPA), a tumor promoter, is a potent inhibitor of inducer-mediated differentiation of murine erythroleukemia cells. Inhibition of cell differentiation was associated with inhibition of cell growth. The present studies, employing a cell line adapted for growth in TPA, demonstrate that inhibition of differentiation is not dependent upon inhibition of cell growth or a change in the cell division cycle; neither is inhibition of differentiation accompanied by detectable effect on cell uptake of [3H]hexamethylene bisacetamide, the inducer used in these studies. TPA causes an inhibition of expression of all hexamethylene bisacetamide-inducible erythroid characteristics measured, including commitment to terminal cell division, accumulation of globin mRNA, and synthesis of globins, spectrin, heme synthetic enzymes (delta-aminolevulinic acid dehydratase and uroporphyrinogen-I synthase) and heme. A hypothetical model for the inhibitory action of tumor promoters on terminal cell differentiation is discussed.
先前的研究表明,肿瘤促进剂十四酰佛波醇-13-乙酸酯(TPA)是诱导剂介导的小鼠红白血病细胞分化的有效抑制剂。细胞分化的抑制与细胞生长的抑制相关。本研究使用了适应于在TPA中生长的细胞系,结果表明分化的抑制并不依赖于细胞生长的抑制或细胞分裂周期的改变;分化的抑制也未伴随着对本研究中所用诱导剂[3H]六亚甲基双乙酰胺的细胞摄取产生可检测到的影响。TPA会抑制所测定的所有六亚甲基双乙酰胺诱导的红系特征的表达,包括对终末细胞分裂的定向、珠蛋白mRNA的积累以及珠蛋白、血影蛋白、血红素合成酶(δ-氨基乙酰丙酸脱水酶和尿卟啉原-I合成酶)和血红素的合成。本文讨论了肿瘤促进剂对终末细胞分化抑制作用的一个假设模型。