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异种移植人胃癌的热耐受性

Thermotolerance of xenografted human gastric cancer.

作者信息

Fujimoto S, Ohta M, Shrestha R D, Kokubun M, Kobayashi K, Kiuchi S, Konno C, Takahashi M, Fujita M, Taguchi T

机构信息

First Department of Surgery, School of Medicine, Chiba University, Japan.

出版信息

Jpn J Surg. 1989 Mar;19(2):203-7. doi: 10.1007/BF02471586.

DOI:10.1007/BF02471586
PMID:2724719
Abstract

To compare the thermotolerance in vivo of two human gastric cancers with different doubling times, the xenografted tumors were warmed twice at 43.5 +/- 0.1 degree C in a water bath for 20 minutes at a predetermined interval. In the tumors with doubling times of 5.2 and 10.9 days, a 7-day interval heat treatment resulted in a prolongation in tumor tripling times by 156 per cent and 132 per cent, respectively, compared with a single heat treatment for 40 minutes. On the contrary, two heat treatments given at intervals of 3 to 5 days had a short tumor tripling time, compared to that of the 40-minute single treatment. Thus, the thermotolerance of these human gastric cancers gradually increased to a maximum within a 3- to 4-day interval and disappeared completely after a 7-day interval. These results indicate that the times required to reach maximal thermotolerance in these human gastric cancers were longer than those previously demonstrated for human and rodent cancer cell lines in vitro. The development and decay of thermotolerance in these human gastric cancers need to be considered in the design of multiple-fractionated regimens.

摘要

为比较两种倍增时间不同的人胃癌在体内的耐热性,将移植瘤在43.5±0.1摄氏度的水浴中按预定间隔进行两次加热,每次20分钟。对于倍增时间分别为5.2天和10.9天的肿瘤,与单次40分钟热处理相比,7天间隔的热处理使肿瘤三倍增长时间分别延长了156%和132%。相反,与40分钟单次处理相比,间隔3至5天进行的两次热处理使肿瘤三倍增长时间缩短。因此,这些人胃癌的耐热性在3至4天的间隔内逐渐增加至最大值,并在7天间隔后完全消失。这些结果表明,这些人胃癌达到最大耐热性所需的时间比先前在体外对人和啮齿动物癌细胞系所证明的时间更长。在设计多分次治疗方案时,需要考虑这些人胃癌中耐热性的产生和消退。

相似文献

1
Thermotolerance of xenografted human gastric cancer.异种移植人胃癌的热耐受性
Jpn J Surg. 1989 Mar;19(2):203-7. doi: 10.1007/BF02471586.
2
Influence of cellular, microenvironmental, and growth parameters on thermotolerance kinetics in vivo in human melanoma xenografts.细胞、微环境和生长参数对人黑色素瘤异种移植瘤体内热耐受动力学的影响。
Cancer Res. 1989 Sep 15;49(18):5027-32.
3
[The relationship between thermotolerance and the tissue oxygen tension in human gastric cancer tissue].[人胃癌组织中热耐受性与组织氧张力之间的关系]
Gan No Rinsho. 1988 Dec;34(15):2075-8.
4
[Polarographic analysis of tumor tissue oxygen tension after hyperthermia combined with misonidazole].
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5
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6
Development of thermotolerance during fractionated hyperthermia in a solid tumor in vivo.体内实体瘤分次热疗过程中热耐受性的发展。
Cancer Res. 1982 May;42(5):1744-8.
7
A combination of Laserthermia and chemotherapy for the treatment human gastric cancers transplanted into nude mice.激光热疗与化疗联合治疗裸鼠移植的人胃癌。
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Local hyperthermia using a low powered Nd: YAG laser for pancreatic and gastric carcinoma.使用低功率钕钇铝石榴石激光对胰腺癌和胃癌进行局部热疗。
Hokkaido Igaku Zasshi. 1988 Nov;63(6):889-96.
9
Enhancement of thermal sensitivity of xenografted human DLD-2 tumors by administration of basic fibroblast growth factor.通过给予碱性成纤维细胞生长因子提高异种移植的人DLD - 2肿瘤的热敏感性。
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10
Thermotolerance induced by fractionated hyperthermia: dependence of the interval between fractions.分次热疗诱导的热耐受性:分次间隔的依赖性
Int J Hyperthermia. 1987 Sep-Oct;3(5):433-9. doi: 10.3109/02656738709140413.

本文引用的文献

1
The induction of thermal resistance in the ear of the mouse by heating at temperatures ranging from 41.5 to 45.5 degrees C.通过在41.5至45.5摄氏度的温度范围内加热来诱导小鼠耳部产生热抗性。
Radiat Res. 1981 Jan;85(1):126-34.
2
The effect of hyperthermia on vascular function, pH, and cell survival.热疗对血管功能、pH值和细胞存活的影响。
Radiology. 1980 Dec;137(3):795-803. doi: 10.1148/radiology.137.3.7444064.
3
Effects of hyperthermia on normal and tumor microenvironment.热疗对正常和肿瘤微环境的影响。
Radiology. 1980 Nov;137(2):523-30. doi: 10.1148/radiology.137.2.7433686.
4
Importance of preheating temperature and time for the induction of thermotolerance in a solid tumour in vivo.体内实体瘤中诱导热耐受时预热温度和时间的重要性。
Br J Cancer. 1982 Dec;46(6):894-903. doi: 10.1038/bjc.1982.299.
5
Synthesis and degradation of heat shock proteins during development and decay of thermotolerance.热耐受性发育和衰退过程中热休克蛋白的合成与降解
Cancer Res. 1982 Jun;42(6):2457-61.
6
Development of thermotolerance during fractionated hyperthermia in a solid tumor in vivo.体内实体瘤分次热疗过程中热耐受性的发展。
Cancer Res. 1982 May;42(5):1744-8.
7
The role of tissue environmental factors on the kinetics and morphology of tumor cells exposed to hyperthermia.
Ann N Y Acad Sci. 1980;335:254-80. doi: 10.1111/j.1749-6632.1980.tb50753.x.
8
Hyperthermia and the heat-shock proteins of HeLa cells.HeLa细胞的热疗与热休克蛋白
Br J Cancer. 1982 Jun;45(6):953-63. doi: 10.1038/bjc.1982.148.
9
Development of thermotolerance in a human melanoma xenograft.
Cancer Res. 1984 Feb;44(2):525-30.
10
Clinical effects of total-body hyperthermia combined with anticancer chemotherapy for far-advanced gastrointestinal cancer.全身热疗联合抗癌化疗治疗晚期胃肠道癌的临床疗效
Cancer. 1985 Apr 15;55(8):1641-7. doi: 10.1002/1097-0142(19850415)55:8<1641::aid-cncr2820550805>3.0.co;2-v.