Singh N, Aggarwal S
Department of Biochemistry, All India Institute of Medical Sciences, New Delhi.
Int J Cancer. 1995 Jul 4;62(1):107-14. doi: 10.1002/ijc.2910620120.
To gain insight into the gene regulation and signal transduction effects of active oxygen in tumour promotion and progression, we studied the effect of active oxygen generated extracellularly by xanthine/xanthine oxidase (X/XO) in promotion-insensitive (P-), promotion-sensitive (P+) and transformed (Tx) mouse epidermal JB6 cells. Active oxygen inhibited growth, particularly of P- cells and increased poly ADPR transferase activity and PKC activity more significantly in P- cells. No phenotypic differences in the distribution pattern of PKC isotypes alpha, beta and gamma were seen in JB6 cells. PKC alpha was expressed abundantly, whereas beta and gamma were not detected. Basal levels of the antioxidant enzymes catalase and CuZn. Superoxide dismutase were higher in P+ and Tx cells. X/XO resulted in an initial decrease in the activity of these enzymes, followed by recovery or transient induction in Tx and P+ cells. X/XO induced c-myc and c-fos expression in JB6 cells, with c-fos induction being more pronounced in P- cells, whereas a biphasic increase in c-jun was seen in P+ cells. These early genes may play a role in proliferation whereas post-translational poly ADP-ribosylation and, perhaps, phosphorylation suggest a genetic-epigenetic mechanism in oxidant tumour promotion and progression.
为深入了解活性氧在肿瘤促进和进展过程中的基因调控及信号转导作用,我们研究了黄嘌呤/黄嘌呤氧化酶(X/XO)在促进不敏感(P-)、促进敏感(P+)和转化(Tx)的小鼠表皮JB6细胞中细胞外产生的活性氧的作用。活性氧抑制细胞生长,尤其是P-细胞的生长,并更显著地增加P-细胞中的多聚ADPR转移酶活性和PKC活性。在JB6细胞中未观察到PKC同工型α、β和γ分布模式的表型差异。PKCα大量表达,而未检测到β和γ。抗氧化酶过氧化氢酶和铜锌超氧化物歧化酶的基础水平在P+和Tx细胞中较高。X/XO导致这些酶的活性最初下降,随后在Tx和P+细胞中恢复或短暂诱导。X/XO诱导JB6细胞中c-myc和c-fos的表达,c-fos的诱导在P-细胞中更明显,而在P+细胞中c-jun呈双相增加。这些早期基因可能在增殖中起作用,而翻译后多聚ADP-核糖基化以及可能的磷酸化表明在氧化剂诱导的肿瘤促进和进展中存在一种遗传-表观遗传机制。