Sunkara P S, Chang C C, Prakash N J, Lachmann P J
Cancer Res. 1985 Sep;45(9):4067-70.
The objective of the present study was to investigate the effect of polyamine depletion by alpha-difluoromethylornithine (DFMO), a specific irreversible inhibitor of ornithine decarboxylase, on the growth and differentiation of B16 melanoma cells grown in culture and also as solid tumors in mice. Polyamine depletion by DFMO (2.5 mM) resulted in a complete inhibition of cell growth in culture and a 90% inhibition of viability of melanoma cells as determined by clonogenic assay at the end of 7 days after DFMO treatment. These results indicate that polyamine depletion induced by DFMO is cytotoxic to B16 melanoma cells in culture. Furthermore a 2- to 5-fold increase in tyrosinase activity and 10-fold accumulation of melanine were observed in polyamine depleted cells compared to control cultures. These effects of DFMO could easily be reversed by the addition of putrescine simultaneously with DFMO. Administration of different doses of DFMO in drinking water to B16 melanoma tumor bearing mice also resulted in an increase in tyrosinase activity and a dose dependent inhibition (86-90%) of tumor growth. Although one cannot rule out the possibility of induction of differentiated phenotype as a result of antiproliferative activity of DFMO, the data presented indicate that the unique sensitivity of melanoma to DFMO may be due to a combination of cell growth inhibition and concomitant induction of differentiation upon polyamine depletion. The results of the present study indicate that polyamines play an important role in growth and differentiation of melanoma and also provide an example of inhibition of tumor cell growth by induction of cellular differentiation.
本研究的目的是调查鸟氨酸脱羧酶的特异性不可逆抑制剂α-二氟甲基鸟氨酸(DFMO)导致的多胺耗竭对培养的B16黑色素瘤细胞以及小鼠体内实体瘤生长和分化的影响。DFMO(2.5 mM)导致的多胺耗竭在培养中完全抑制了细胞生长,并且在DFMO处理7天后通过克隆形成试验测定,黑色素瘤细胞的活力受到了90%的抑制。这些结果表明,DFMO诱导的多胺耗竭对培养中的B16黑色素瘤细胞具有细胞毒性。此外,与对照培养物相比,在多胺耗竭的细胞中观察到酪氨酸酶活性增加了2至5倍,黑色素积累增加了10倍。DFMO的这些作用可通过与DFMO同时添加腐胺而轻易逆转。给携带B16黑色素瘤肿瘤的小鼠饮用不同剂量的DFMO也导致酪氨酸酶活性增加以及肿瘤生长的剂量依赖性抑制(86 - 90%)。尽管不能排除由于DFMO的抗增殖活性诱导分化表型的可能性,但所呈现的数据表明,黑色素瘤对DFMO的独特敏感性可能是由于细胞生长抑制和多胺耗竭时伴随的分化诱导共同作用的结果。本研究结果表明,多胺在黑色素瘤的生长和分化中起重要作用,并且还提供了一个通过诱导细胞分化抑制肿瘤细胞生长的例子。