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1
Can cell survival parameters be deduced from non clonogenic assays of radiation damage to normal tissues?能否从正常组织辐射损伤的非克隆形成试验中推断细胞存活参数?
Br J Cancer Suppl. 1984;6:257-61.
2
A critical appraisal of clonogenic survival assays in the evaluation of radiation damage to normal tissues.对克隆形成存活试验在评估正常组织辐射损伤中的批判性评价。
Radiother Oncol. 1984 Jan;1(3):241-6. doi: 10.1016/s0167-8140(84)80006-7.
3
[The capacity of rat clonogenic precursor cells of the hemopoietic stroma (CFU-F) to recover from radiation damages].[大鼠造血基质克隆前体细胞(CFU-F)从辐射损伤中恢复的能力]
Radiobiologiia. 1993 Mar-Apr;33(2):236-43.
4
Dose response curves for clonogenic cell survival or functional impairment of irradiated normal tissues.克隆形成细胞存活或受照射正常组织功能损伤的剂量反应曲线。
Br J Radiol. 1984 Jan;57(673):105. doi: 10.1259/0007-1285-57-673-105.
5
Effects of radiation on normal tissues: hypothetical mechanisms and limitations of in situ assays of clonogenicity.辐射对正常组织的影响:克隆形成能力原位检测的假设机制及局限性
Radiat Environ Biophys. 1981;19(3):157-72. doi: 10.1007/BF01324183.
6
Recovery from potentially lethal damage and recruitment time of noncycling clonogenic cells in 9L confluent monolayers and spheroids.9L汇合单层细胞和球体中潜在致死性损伤的恢复及非循环克隆形成细胞的招募时间。
Radiat Res. 1988 Jun;114(3):515-27.
7
[The effect of the gas hypoxic mixture GHM-8 on the capacity of the stromal clonogenic cells (CFU-F) in rat bone marrow for postradiation recovery].
Radiobiologiia. 1993 Mar-Apr;33(2):244-54.
8
Can dose-survival parameters be deduced from in situ assays?能否从原位分析中推断出剂量-存活参数?
Br J Cancer Suppl. 1980 Apr;4:79-87.
9
Response to continuous irradiation (CI) in relation to the initial slope of the cell survival curve for tumours and bone marrow.肿瘤和骨髓细胞存活曲线初始斜率与连续照射(CI)的反应
Br J Cancer Suppl. 1984;6:271-4.
10
[Thermosensitivity of clonogenic cells and the induction of thermal tolerance].[克隆形成细胞的热敏感性及热耐受的诱导]
Med Radiol (Mosk). 1987 Jan;32(1):67-9.

引用本文的文献

1
Assays of damage to the alimentary canal.消化道损伤检测
Br J Cancer Suppl. 1986;7:1-6.
2
Alternative models for the proliferative structure of normal tissues and their response to irradiation.正常组织增殖结构及其对辐射反应的替代模型。
Br J Cancer Suppl. 1986;7:382-5.
3
Cell kinetics and radiation pathology.细胞动力学与放射病理学
Experientia. 1989 Jan 15;45(1):33-41. doi: 10.1007/BF01990450.
4
Early and late changes in the normal mouse bladder reservoir function due to irradiation and cis-DDP.放疗和顺铂对正常小鼠膀胱储尿功能的早期及晚期影响
Br J Cancer. 1992 Jul;66(1):99-105. doi: 10.1038/bjc.1992.224.

本文引用的文献

1
Radiation effects on cell renewal and related systems.辐射对细胞更新及相关系统的影响。
Physiol Rev. 1963 Jul;43:357-96. doi: 10.1152/physrev.1963.43.3.357.
2
Comparative mortality following single whole-body exposures of mice to fission neutrons and Co60 gamma rays.小鼠单次全身暴露于裂变中子和钴60γ射线后的比较死亡率。
Radiology. 1957 Mar;68(3):386-98. doi: 10.1148/68.3.386.
3
Action of x-rays on mammalian cells.X射线对哺乳动物细胞的作用。
J Exp Med. 1956 May 1;103(5):653-66. doi: 10.1084/jem.103.5.653.
4
The effect of irradiation on function in self-renewing normal tissues with differing proliferative organisation.辐射对具有不同增殖组织的自我更新正常组织功能的影响。
Br J Radiol. 1982 Oct;55(658):759-66. doi: 10.1259/0007-1285-55-658-759.
5
Histologic examination of the influence of dietary protein on rat radiation nephropathy.
Radiat Res. 1982 Mar;89(3):546-58.
6
Early and late pulmonary toxicity in mice evaluated 180 and 420 days following localized lung irradiation.
Radiat Res. 1982 Feb;89(2):396-407.
7
Dose-dependence of the time of appearance of lung damage in mice given thoracic irradiation.给予胸部照射的小鼠肺部损伤出现时间的剂量依赖性。
Int J Radiat Biol Relat Stud Phys Chem Med. 1982 Sep;42(3):245-52. doi: 10.1080/09553008214551171.
8
A quantitative technique for measuring renal damage after irradiation.一种测量辐射后肾损伤的定量技术。
Radiology. 1973 Nov;109(2):457-62. doi: 10.1148/109.2.457.
9
A cell kinetic model to explain the time of appearance of skin reaction after X-rays or ultraviolet light irradiation.一种细胞动力学模型,用于解释X射线或紫外线照射后皮肤反应出现的时间。
Cell Tissue Kinet. 1979 May;12(3):281-9. doi: 10.1111/j.1365-2184.1979.tb00150.x.

能否从正常组织辐射损伤的非克隆形成试验中推断细胞存活参数?

Can cell survival parameters be deduced from non clonogenic assays of radiation damage to normal tissues?

作者信息

Michalowski A, Wheldon T E, Kirk J

出版信息

Br J Cancer Suppl. 1984;6:257-61.

PMID:6582914
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2149134/
Abstract

Though dose-response curves for large scale radiation injury to tissues are undoubtedly related to survival curves for clonogenic cells, the relationship between the two sets of curves is not necessarily simple. Sterilization of clonogenic cells occurs near-instantaneously by comparison with the protracted lag period for gross injury to tissues. Moreover, with some types of macroscopic damage, the shapes of the dose-response curves may depend on time of assay. Changes in the area or volume of irradiated tissue may also influence the shapes of these curves. The temporal pattern of expression of large scale injury also varies between tissues, and two distinct groups can be recognized. In rapidly proliferating tissues, the lag period is almost independent of dose, whilst in slowly proliferating tissues, it is inversely proportional to dose. This might be explained by invoking differences in corresponding proliferative structures of the tissues (Three compartmental Type H versus One compartmental Type F proliferative organization). For the second group of tissues, in particular, mathematical modelling suggests a systematic dissociation of the dose-response curves for clonogenic cell survival and for large scale injury. This dissociation, which arises even in the case of single doses, may be even more important when radiation is fractionated. In particular, it may be difficult to disentangle the contributions made to inter-fraction sparing by cellular repair processes and by proliferation-related factors.

摘要

尽管组织大规模辐射损伤的剂量反应曲线无疑与克隆细胞的存活曲线相关,但这两组曲线之间的关系不一定简单。与组织出现明显损伤的漫长延迟期相比,克隆细胞的失活几乎是瞬间发生的。此外,对于某些类型的宏观损伤,剂量反应曲线的形状可能取决于检测时间。受照射组织面积或体积的变化也可能影响这些曲线的形状。大规模损伤的表达时间模式在不同组织之间也有所不同,可分为两个不同的组。在快速增殖组织中,延迟期几乎与剂量无关,而在缓慢增殖组织中,延迟期与剂量成反比。这可能是由于组织相应增殖结构的差异(三室H型与一室F型增殖组织)所致。特别是对于第二组组织,数学模型表明克隆细胞存活和大规模损伤的剂量反应曲线存在系统性分离。这种分离即使在单次剂量照射的情况下也会出现,当进行分次照射时可能更为重要。特别是,可能难以区分细胞修复过程和增殖相关因素对分次照射时剂量节省的贡献。