Olinski R, Jaruga P, Zastawny T H
Department of Clinical Biochemistry, The Ludwik Rydygier Medical University in Bydgoszcz, Poland.
Acta Biochim Pol. 1998;45(2):561-72.
Reactive oxygen species can cause extensive DNA modifications including modified bases. Some of the DNA base damage has been found to possess premutagenic properties. Therefore, if not repaired, it can contribute to carcinogenesis. We have found elevated amounts of modified bases in cancerous and precancerous tissues as compared with normal tissues. Most of the agents used in anticancer therapy are paradoxically responsible for induction of secondary malignancies and some of them may generate free radicals. The results of our experiments provide evidence that exposure of cancer patients to therapeutic doses of ionizing radiation and anticancer drugs causes base modifications in genomic DNA of lymphocytes. Some of these base damages could lead to mutagenesis in critical genes and ultimately to secondary cancers such as leukemias. This may point to an important role of oxidative base damage in cancer initiation. Alternatively, the increased level of the modified base products may contribute to genetic instability and metastatic potential of tumor cells.
活性氧可导致广泛的DNA修饰,包括碱基修饰。已发现某些DNA碱基损伤具有致突变前的特性。因此,如果不进行修复,它可能会导致癌症发生。我们发现,与正常组织相比,癌组织和癌前组织中的修饰碱基含量升高。矛盾的是,大多数用于抗癌治疗的药物会导致继发性恶性肿瘤的发生,其中一些药物可能会产生自由基。我们的实验结果表明,癌症患者接受治疗剂量的电离辐射和抗癌药物会导致淋巴细胞基因组DNA中的碱基修饰。其中一些碱基损伤可能会导致关键基因发生突变,并最终导致白血病等继发性癌症。这可能表明氧化碱基损伤在癌症发生中起重要作用。或者,修饰碱基产物水平的升高可能会导致肿瘤细胞的遗传不稳定和转移潜能。