Lamprecht S A, Schwartz B, Avigdor A, Guberman R
Gastroenterology Laboratory, Soroka Medical Center, Beer-Sheva, Israel.
Anticancer Res. 1990 May-Jun;10(3):773-8.
The activities of the growth-related enzymes ornithine decarboxylase (ODC) and casein kinase II (CK-II) were assayed along the colon crypt axis in a precise temporal sequence following administration of 1,2-dimethylhydrazine (DMH) to male rats. The time course of events monitored in colonic cell populations sequentially harvested by a scraping procedure shows that the potent carcinogenic insult induces an early and late ODC activity peak: the distinct biphasic response of the decarboxylase was observed in all colonic crypt compartments. The activity gradient of CK-II was markedly altered in DMH-treated cell populations: brisk activity of the kinase was observed in the upper crypt zone, the preserve of the mature, non-dividing colonocyte. The enhanced responses of ODC and of CK-II to DMH proceeded the actual polyp and tumor formation. The polycations spermine and spermidine, bioactive molecules formed in the ODC-controlled polyamine pathway, were shown to markedly activate colonic CK-II. This observation suggests that ODC and CK-II, enzymes with different catalytic purposes, crosstalk within the colonic crypt continuum. The present findings indicate that the differentiation arrest of colonic cells and their misplacement in forbidden zones of the crypt axis during DMH-induced carcinogenesis is accompanied by early alterations in the activity and topology of disparate enzymes which are part of the orderly growth program of the normal colonic cell.
在给雄性大鼠注射1,2 - 二甲基肼(DMH)后,按照精确的时间顺序,沿着结肠隐窝轴对与生长相关的鸟氨酸脱羧酶(ODC)和酪蛋白激酶II(CK-II)的活性进行了测定。通过刮取程序依次收获结肠细胞群体来监测事件的时间进程,结果表明,强烈的致癌刺激诱导了ODC活性的早期和晚期峰值:在所有结肠隐窝区室中均观察到脱羧酶明显的双相反应。在经DMH处理的细胞群体中,CK-II的活性梯度发生了显著改变:在隐窝上部区域观察到激酶的活跃活性,该区域是成熟的、不分裂的结肠细胞所在之处。ODC和CK-II对DMH的增强反应先于实际的息肉和肿瘤形成。在ODC控制的多胺途径中形成的生物活性分子多阳离子精胺和亚精胺,被证明能显著激活结肠CK-II。这一观察结果表明,具有不同催化功能的ODC和CK-II在结肠隐窝连续体中相互作用。目前的研究结果表明在DMH诱导的致癌过程中,结肠细胞的分化停滞及其在隐窝轴禁区的错位伴随着不同酶的活性和拓扑结构的早期改变,这些酶是正常结肠细胞有序生长程序的一部分。