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辐射诱导的细胞凋亡及其与克隆存活丧失的关系。

Radiation-induced apoptosis and its relationship to loss of clonogenic survival.

作者信息

Held K D

机构信息

Department of Radiation Oncology, Massachusetts General Hospital, Harvard Medical School, Boston 02114, USA.

出版信息

Apoptosis. 1997;2(3):265-82. doi: 10.1023/a:1026485003280.

Abstract

Ionizing radiation can be an effective inducer of apoptosis and studies of many aspects of the pathways and mechanisms involved in this apoptosis induction have been published. This review stresses two aspects: the relationship between apoptosis and loss of clonogenic ability in irradiated cells and the time course for the appearance of apoptosis after radiation exposure. Although it was initially assumed that apoptosis occurred relatively quickly (within hours) after irradiation, evidence is presented and discussed here showing that apoptosis can occur at long times after irradiation (out to 20 days) in some cell types. This late, or delayed, apoptosis occurs after the cells have divided once or several times. The impact of delayed apoptosis on loss of clonogenicity after irradiation remains unclear. It seems likely that in some cell types, e.g., fibroblasts, the occurrence of late apoptosis is minimal and may have little impact on long term cell survival of the population, but in at least one instance, with a cell line of hematopoietic origin, it appears that late apoptosis can account for all the loss of clonogenicity in irradiated cells. The role of p53 in radiation-induced apoptosis is also discussed, with data presented showing that both p53-dependent and independent pathways for radiation-induced apoptosis exist, depending on the cell type.

摘要

电离辐射可以有效地诱导细胞凋亡,并且关于这种凋亡诱导所涉及的途径和机制的许多方面的研究已经发表。本综述强调两个方面:照射后细胞凋亡与克隆形成能力丧失之间的关系以及辐射暴露后凋亡出现的时间进程。尽管最初认为凋亡在照射后相对较快(数小时内)发生,但这里展示并讨论了证据,表明在某些细胞类型中,凋亡可在照射后很长时间(长达20天)发生。这种晚期或延迟凋亡发生在细胞分裂一次或几次之后。照射后延迟凋亡对克隆形成能力丧失的影响仍不清楚。在某些细胞类型中,例如成纤维细胞,似乎晚期凋亡的发生极少,可能对群体的长期细胞存活影响很小,但至少在一个实例中,对于一种造血来源的细胞系,似乎晚期凋亡可以解释照射后细胞克隆形成能力的全部丧失。还讨论了p53在辐射诱导凋亡中的作用,所呈现的数据表明,根据细胞类型的不同,辐射诱导凋亡存在p53依赖和非依赖途径。

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