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细胞存活是9L肿瘤原位反应的决定因素吗?

Is cell survival a determinant of the in situ response of 9L tumours?

作者信息

Wheeler K T, Wallen C A

出版信息

Br J Cancer Suppl. 1980 Apr;4:299-303.

PMID:6932940
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2149259/
Abstract

The influence fo growth rate, location, size and PLD recovery on the cellular radiosensitivity, the tumour response (increase in life-span) and the relationship between these two end points was studied using two sublines of the 9L rat brain tumour, designated 9L/Ro and 9L/SF. The median day of death of rats bearing the intracerebral (i.c.) 9L/Ro tumours was 16-18 days; for i.c. 9L/SF tumours it was 23-25 days. The doubling time of 9L/Ro cells was slightly faster than that for 9L/SF cells both in culture and in the brain. The cellular radiosensitivity of both i.c. tumour cell sublines was identical when measured immediately after irradiation by an in vitro colony formation assay. However, subcutaneous (s.c.) 9L/Ro tumour cells were more resistant (D0 = 332 rad cf 180 rad). There was no evidence of a substantial hypoxic fraction in either site. When i.c. 9L/Ro and 9L/SF tumours of similar size were treated with fractionated doses of BCNU, X-rays or combinations of the two, the responses of the two tumours were essentially identical. The rate of recovery from radiation-induced potentially lethal damage (PLD) was identical in the two sublines and the two sites, although the extent of the PLD recovery was apparently greater in s.c. tumours. Increase in life-span of rats bearing i.c. 9L/Ro tumours appeared to be correlated with the tumour cell kill measured after completion of PLD recovery rather than with the tumour cell kill determined immediately after irradiation.

摘要

利用9L大鼠脑肿瘤的两个亚系(分别命名为9L/Ro和9L/SF),研究了生长速率、位置、大小和潜在致死性损伤(PLD)修复对细胞放射敏感性、肿瘤反应(寿命延长)以及这两个终点之间关系的影响。携带脑内(i.c.)9L/Ro肿瘤的大鼠的中位死亡天数为16 - 18天;对于脑内9L/SF肿瘤,中位死亡天数为23 - 25天。9L/Ro细胞在培养中和脑内的倍增时间均略快于9L/SF细胞。通过体外集落形成试验在照射后立即测量时,两个脑内肿瘤细胞亚系的细胞放射敏感性相同。然而,皮下(s.c.)9L/Ro肿瘤细胞更具抗性(D0 = 332拉德,而9L/SF为180拉德)。在两个部位均未发现大量缺氧部分的证据。当用分次剂量的卡莫司汀(BCNU)、X射线或两者组合治疗大小相似的脑内9L/Ro和9L/SF肿瘤时,两种肿瘤的反应基本相同。两个亚系和两个部位从辐射诱导的潜在致死性损伤(PLD)中的修复速率相同,尽管皮下肿瘤中PLD修复的程度明显更大。携带脑内9L/Ro肿瘤的大鼠寿命延长似乎与PLD修复完成后测量的肿瘤细胞杀伤相关,而非与照射后立即确定的肿瘤细胞杀伤相关。

相似文献

1
Is cell survival a determinant of the in situ response of 9L tumours?细胞存活是9L肿瘤原位反应的决定因素吗?
Br J Cancer Suppl. 1980 Apr;4:299-303.
2
Relationship between the repair of radiation-induced DNA damage and recovery from potentially lethal damage in 9L rat brain tumor cells.
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3
Response of 9L rat brain tumor multicellular spheroids to single and fractionated doses of 1,3-bis(2-chloroethyl)-1-nitrosourea.9L大鼠脑肿瘤多细胞球体对单次和分次剂量1,3-双(2-氯乙基)-1-亚硝基脲的反应
Cancer Res. 1984 Feb;44(2):571-6.
4
Combination therapy with 1,3-bis(2-chloroethyl)-1-nitrosourea and low dose rate radiation in the 9L rat brain tumor and spheroid models: implications for brain tumor brachytherapy.
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Hypoxic cells and in situ chemopotentiation of the nitrosoureas by misonidazole.缺氧细胞与米索硝唑对亚硝基脲的原位化学增敏作用。
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Radiat Res. 1980 Sep;83(3):633-43.
9
The effect of radiation on tumour growth delay, cell survival and cure of the animal using a single tumour system.使用单一肿瘤系统研究辐射对动物肿瘤生长延迟、细胞存活及治愈情况的影响。
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10
Radiobiological studies of tumours in situ compared with cell survival.原位肿瘤与细胞存活的放射生物学研究。
Br J Cancer Suppl. 1980 Apr;4:259-65.

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本文引用的文献

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Development of an in vitro colony formation assay for the evaluation of in vivo chemotherapy of a rat brain tumor.用于评估大鼠脑肿瘤体内化疗效果的体外集落形成试验的开发。
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Factors influencing the survival of rat brain tumor cells after in vitro treatment with 1,3-bis(2-chloroethyl)-1-nitrosourea.体外经1,3-双(2-氯乙基)-1-亚硝基脲处理后影响大鼠脑肿瘤细胞存活的因素
Cancer Res. 1975 Jun;35(6):1464-9.
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In vitro evaluation of in vivo brain tumor chemotherapy with 1,3-bis(2-chloroethyl)-1-nitrosourea.1,3-双(2-氯乙基)-1-亚硝基脲对体内脑肿瘤化疗的体外评估
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