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化学致癌作用中的自由基

Free radicals in chemical carcinogenesis.

作者信息

Clemens M R

机构信息

Abteilung Innere Medizin II, Eberhard-Karls-Universität Tübingen.

出版信息

Klin Wochenschr. 1991 Dec 15;69(21-23):1123-34. doi: 10.1007/BF01645172.

Abstract

During the past decade, remarkable progress has been made in our understanding of cancer-causing agents, mechanisms of cancer formation and the behavior of cancer cells. Cancer is characterized primarily by an increase in the number of abnormal cells derived from a given normal tissue, invasion of adjacent tissues by these abnormal cells, and lymphatic or blood-borne spread of malignant cells to regional lymph nodes and to distant sites (metastasis). It has been estimated that about 75-80% of all human cancers are environmentally induced, 30-40% of them by diet. Only a small minority, possibly no more than 2% of all cases, result purely from inherent genetic changes. Several lines of evidence confirm that the fundamental molecular event or events that cause a cell to become malignant occur at the level of the DNA and a variety of studies indicate that the critical molecular event in chemical carcinogenesis is the interaction of the chemical agent with DNA. The demonstration that DNA isolated from tumor cells can transfect normal cells and render them neoplastic provides direct proof that an alteration of the DNA is responsible for cancer. The transforming genes, or oncogenes, have been identified by restriction endonuclease mapping. One of the characteristics of tumor cells generated by transformation with viruses, chemicals, or radiation is their reduced requirement for serum growth factors. A critical significance of electrophilic metabolites of carcinogenes in chemical carcinogenesis has been demonstrated. A number of "proximate" and "ultimate" metabolites, especially those of aromatic amines, were described. The "ultimate" forms of carcinogens actually interact with cellular constituents to cause neoplastic transformation and are the final metabolic products in most pathways. Recent evidence indicates that free radical derivatives of chemical carcinogens may be produced both metabolically and nonenzymatically during their metabolism. Free radicals carry no charge but do possess a single unpaired electron, making the radical extremely reactive. That such forms may be important in the introduction of neoplastic transformation by chemicals from two lines of evidence. (1) Various molecules that inhibit the formation of free radicals, many of which are termed antioxidants, can inhibit the carcinogenic action of a variety of chemical carcinogens. (2) There are relatively specific metabolic reactions of certain chemical carcinogens, particularly of polycyclic hydrocarbons, for which it has been shown to proceed through free radical intermediates. In conclusion, free radical processes with direct effects on DNA can be proposed for a variety of human and animal carcinogens.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

在过去十年中,我们对致癌物质、癌症形成机制以及癌细胞行为的理解取得了显著进展。癌症的主要特征是源自特定正常组织的异常细胞数量增加、这些异常细胞侵袭相邻组织以及恶性细胞通过淋巴或血液扩散至局部淋巴结和远处部位(转移)。据估计,所有人类癌症中约75 - 80%是由环境因素诱发的,其中30 - 40%是由饮食引起的。只有极少数情况,可能不超过所有病例的2%,纯粹是由内在基因变化导致的。多条证据证实,导致细胞恶变的一个或多个基本分子事件发生在DNA水平,并且各种研究表明化学致癌作用中的关键分子事件是化学物质与DNA的相互作用。从肿瘤细胞中分离出的DNA能够转染正常细胞并使其发生肿瘤性转化,这一事实提供了直接证据,证明DNA的改变是癌症的病因。通过限制性内切酶图谱分析已经鉴定出了转化基因,即癌基因。用病毒、化学物质或辐射转化产生的肿瘤细胞的一个特征是它们对血清生长因子的需求降低。已经证明致癌物的亲电子代谢产物在化学致癌过程中具有关键意义。描述了许多“近端”和“最终”代谢产物,尤其是芳香胺的代谢产物。致癌物的“最终”形式实际上与细胞成分相互作用以导致肿瘤性转化,并且是大多数代谢途径中的最终代谢产物。最近的证据表明,化学致癌物的自由基衍生物在其代谢过程中可能通过代谢和非酶促方式产生。自由基不带电荷,但确实具有一个未成对的单电子,这使得自由基极具反应性。从两方面证据表明这些形式在化学物质引发肿瘤性转化过程中可能很重要。(1)各种抑制自由基形成的分子,其中许多被称为抗氧化剂,能够抑制多种化学致癌物的致癌作用。(2)某些化学致癌物,特别是多环烃,存在相对特定的代谢反应,已表明这些反应通过自由基中间体进行。总之,对于多种人类和动物致癌物,可以提出对DNA有直接影响的自由基过程。(摘要截取自400字)

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