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1
The oncogenic potential of a combination of hyperthermia and chemotherapy agents.热疗与化疗药物联合使用的致癌潜力。
Br J Cancer. 1988 Jan;57(1):59-63. doi: 10.1038/bjc.1988.9.
2
Trimodality therapy (drug/hyperthermia/radiation) with BCNU or mitomycin C.采用卡氮芥或丝裂霉素C的三联疗法(药物/热疗/放疗)。
Int J Radiat Oncol Biol Phys. 1990 Feb;18(2):375-82. doi: 10.1016/0360-3016(90)90103-q.
3
Hyperthermia, chemotherapeutic agents and oncogenic transformation.热疗、化疗药物与致癌转化
Int J Hyperthermia. 1986 Jul-Sep;2(3):311-20. doi: 10.3109/02656738609016488.
4
X-ray induction of O6-alkylguanine-DNA alkyltransferase protects against some of the biological effects of N-methyl-N'-nitro-N-nitrosoguanidine in C3H 10T1/2 cells.X射线诱导的O6-烷基鸟嘌呤-DNA烷基转移酶可保护C3H 10T1/2细胞免受N-甲基-N'-硝基-N-亚硝基胍某些生物学效应的影响。
Radiat Res. 1991 Aug;127(2):220-5.
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Interaction of hyperthermia and chemotherapy agents; cell lethality and oncogenic potential.热疗与化疗药物的相互作用;细胞致死率和致癌潜力。
Int J Hyperthermia. 1994 Jan-Feb;10(1):89-99. doi: 10.3109/02656739409009335.
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Hyperthermic enhancement of cell killing by mitomycin C in mitomycin C-resistant Chinese hamster ovary cells.丝裂霉素C对耐丝裂霉素C的中国仓鼠卵巢细胞杀伤作用的热增强效应
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Oncogenic transformation systems involving mammalian cells in vitro to determine the relative risks of different treatment modalities.
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Effects of hyperthermia on DNA interstrand crosslinking after treatment with BCNU in 9L rat brain tumor cells.
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引用本文的文献

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The combined effects of high-energy shock waves and cytostatic drugs or cytokines on human bladder cancer cells.高能冲击波与细胞毒性药物或细胞因子对人膀胱癌细胞的联合作用。
Br J Cancer. 1994 Jan;69(1):58-65. doi: 10.1038/bjc.1994.9.
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Modulating factors in the expression of radiation-induced oncogenic transformation.辐射诱导致癌转化表达中的调节因素。
Environ Health Perspect. 1990 Aug;88:149-55. doi: 10.1289/ehp.9088149.

本文引用的文献

1
Oncogenic transformation and hyperthermia.致癌转化与热疗。
Br J Radiol. 1980 May;53(629):479-82. doi: 10.1259/0007-1285-53-629-479.
2
Antipain, but not cycloheximide, suppresses radiation transformation when present for only one day at five days post-irradiation.
Carcinogenesis. 1982;3(9):1093-5. doi: 10.1093/carcin/3.9.1093.
3
Biological effects of heat.热的生物学效应。
Cancer Res. 1984 Oct;44(10 Suppl):4708s-4713s.
4
An update on the anticancer effects of a combination of chemotherapy and hyperthermia.化疗与热疗联合应用的抗癌作用最新进展
Cancer Res. 1984 Oct;44(10 Suppl):4853s-4856s.
5
Quantitative and qualitative studies of chemical transformation of cloned C3H mouse embryo cells sensitive to postconfluence inhibition of cell division.对汇合后细胞分裂抑制敏感的克隆C3H小鼠胚胎细胞化学转化的定量和定性研究。
Cancer Res. 1973 Dec;33(12):3239-49.
6
Establishment and characterization of a cloned line of C3H mouse embryo cells sensitive to postconfluence inhibition of division.对汇合后分裂抑制敏感的C3H小鼠胚胎细胞克隆系的建立与鉴定
Cancer Res. 1973 Dec;33(12):3231-8.
7
Protein synthesis, thermotolerance and step down heating.蛋白质合成、耐热性与逐步降温加热
Int J Radiat Oncol Biol Phys. 1985 Jan;11(1):159-64. doi: 10.1016/0360-3016(85)90375-x.
8
Oncogenic transformation with radiation and chemicals.辐射与化学物质导致的致癌转化。
Int J Radiat Biol Relat Stud Phys Chem Med. 1985 Jul;48(1):1-18. doi: 10.1080/09553008514551021.

热疗与化疗药物联合使用的致癌潜力。

The oncogenic potential of a combination of hyperthermia and chemotherapy agents.

作者信息

Komatsu K, Miller R C, Hall E J

机构信息

Department of Radiation Oncology, College of Physicians & Surgeons of Columbia University, New York, NY 10032.

出版信息

Br J Cancer. 1988 Jan;57(1):59-63. doi: 10.1038/bjc.1988.9.

DOI:10.1038/bjc.1988.9
PMID:3126790
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2246689/
Abstract

The modulating effect of 43 degrees C hyperthermia on the induction of oncogenic transformation by the antineoplastic agents, actinomycin D, mitomycin C, and 1,3-bis(2-chloroethyl)-1-nitrosourea (BCNU) was examined using the C3H 10T1/2 cell line. For any given level of cytotoxicity, cells exposed to the three chemotherapy agents at 37 degrees C showed similar frequencies of transformation. Transformation frequencies induced by all three drugs were reduced by hyperthermia. The reduction was most pronounced for cells exposed to BCNU, and to a lesser extent, by cells exposed to actinomycin D and mitomycin C. The modulating effects of heat on drug-induced transformation incidence appeared to be independent of whether application of heat and drug was concurrent or sequential.

摘要

使用C3H 10T1/2细胞系研究了43摄氏度高温对抗肿瘤药物放线菌素D、丝裂霉素C和1,3-双(2-氯乙基)-1-亚硝基脲(BCNU)诱导致癌转化的调节作用。对于任何给定的细胞毒性水平,在37摄氏度下暴露于这三种化疗药物的细胞显示出相似的转化频率。高温降低了所有三种药物诱导的转化频率。对于暴露于BCNU的细胞,这种降低最为明显,而对于暴露于放线菌素D和丝裂霉素C的细胞,降低程度较小。热对药物诱导的转化发生率的调节作用似乎与热和药物的应用是同时进行还是相继进行无关。