Holbrook N J, Liu Y, Fornace A J
Gene Expression and Aging Section, National Institute on Aging, Baltimore, MD 21244, USA.
EXS. 1996;77:273-88. doi: 10.1007/978-3-0348-9088-5_18.
Recently, much progress has been made in defining the signal transduction pathways mediating the cellular response to genotoxic stress. Multiple pathways involving several distinct MAP kinases (ERK, JNK/SAPK, and p38/HOG1) as well as the tumor suppressor protein p53 contribute to the response; the various pathways being differentially activated by particular genotoxic agents. Although both DNA damage and extranuclear events are important in initiating the response, recent evidence suggests the response is controlled primarily through events occurring at the plasma membrane, overlapping significantly with those important in initiating mitogenic responses. Attenuation of the responses appears to be largely controlled through feedback mechanisms involving gene products produced during the activation process.
最近,在确定介导细胞对基因毒性应激反应的信号转导途径方面取得了很大进展。涉及几种不同的丝裂原活化蛋白激酶(ERK、JNK/SAPK和p38/HOG1)以及肿瘤抑制蛋白p53的多种途径参与了这一反应;各种途径被特定的基因毒性剂差异激活。虽然DNA损伤和核外事件在引发反应中都很重要,但最近的证据表明,该反应主要通过质膜上发生的事件来控制,这与引发有丝分裂反应中重要的事件有很大重叠。反应的减弱似乎主要通过涉及激活过程中产生的基因产物的反馈机制来控制。