Rao P M, Laconi E, Vasudevan S, Denda A, Rajagopal S, Rajalakshmi S, Sarma D S
Toxicol Pathol. 1987;15(2):190-3. doi: 10.1177/019262338701500210.
Perturbations in DNA and/or membranes are considered to be important for the carcinogenic process. A search for nutritional and metabolic means of disturbing the homeostasis of DNA and membranes revealed that nucleotide pools offer an exciting possibility. An imbalance in nucleotide pools can exert a two-pronged attack on both DNA and membranes. When given to rats, orotic acid, a precursor of pyrimidine nucleotides, results in an imbalance in nucleotide pools (an increase in uridine nucleotides and a decrease in inosine/adenine nucleotides), alterations in both DNA and membranes, and promotion of carcinogenesis in the liver initiated by chemical carcinogens. Agents such as adenine and allopurinol, which inhibit the metabolism of orotic acid and thereby decrease the formation of uridine nucleotides, and galactosamine, which traps uridine nucleotides, inhibited the promotional effects of orotic acid in the liver. These results suggested that orotic acid needs to be metabolized to uridine nucleotides and the creation of a subsequent imbalance in nucleotide pools is important for the promotional effects of orotic acid. To determine whether the creation of a nucleotide pool imbalance is a more general mechanism of tumor promotion, two lines of approach were investigated. One was to determine the effect of orotic acid on promotion of carcinogenesis in other organs, and the second approach was to determine how to induce nucleotide pool imbalances by means other than orotic acid administration. It is interesting to note that orotic acid promotes carcinogenesis in duodenum initiated by azoxymethane. Regarding the second approach, it became apparent that several metabolic disturbances result in increased orotic acid synthesis and alterations in nucleotide pools.(ABSTRACT TRUNCATED AT 250 WORDS)
DNA和/或细胞膜的扰动被认为对致癌过程至关重要。对干扰DNA和细胞膜稳态的营养和代谢手段的研究发现,核苷酸池提供了一个令人兴奋的可能性。核苷酸池的失衡可对DNA和细胞膜发起双管齐下的攻击。给大鼠喂食嘧啶核苷酸的前体乳清酸,会导致核苷酸池失衡(尿苷核苷酸增加,肌苷/腺嘌呤核苷酸减少)、DNA和细胞膜发生改变,并促进化学致癌物引发的肝脏致癌作用。腺嘌呤和别嘌呤醇等抑制乳清酸代谢从而减少尿苷核苷酸形成的物质,以及捕获尿苷核苷酸的半乳糖胺,均抑制了乳清酸在肝脏中的促进作用。这些结果表明,乳清酸需要代谢为尿苷核苷酸,随后核苷酸池的失衡对乳清酸的促进作用很重要。为了确定核苷酸池失衡的产生是否是肿瘤促进作用更普遍的机制,研究了两条途径。一是确定乳清酸对其他器官致癌作用促进的影响,第二种方法是确定如何通过除给予乳清酸以外的其他方式诱导核苷酸池失衡。值得注意的是,乳清酸促进了由偶氮甲烷引发的十二指肠致癌作用。关于第二种方法,很明显,几种代谢紊乱会导致乳清酸合成增加和核苷酸池改变。(摘要截选至250词)