Cell biological effects of hyperthermia alone or combined with radiation or drugs: A short introduction to newcomers in the field

被引:194
作者
Kampinga, HH
机构
关键词
protein denaturation; protein aggregation; radiosensitization; chemosensitization; heat shock proteins; chaperone activity;
D O I
10.1080/02656730500532028
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hyperthermia results in protein unfolding that, if not properly chaperoned by Heat Shock Proteins (HSP), can lead to irreversible and toxic protein aggregates. Elevating HSP prior to heating makes cells thermotolerant. Hyperthermia also can enhance the sensitivity of cells to radiation and drugs. This sensitization to drugs or radiation is not directly related to altered HSP expression. However, altering HSP expression before heat and radiation or drug treatment will affect the extent of thermal sensitization because the HSP will attenuate the heat-induced protein damage that is responsible for radiation- or drug-sensitization. For thermal radiosensitization, nuclear protein damage is considered to be responsible for hyperthermic effects on DNA repair, in particular base excision repair. Hyperthermic drug sensitization can be seen for a number of anti-cancer drugs, especially of alkylating agents. Synergy between heat and drugs may arise from multiple events such as heat damage to ABC transporters (drug accumulation), intra-cellular drug detoxification pathways and repair of drug-induced DNA adducts. This may be why cells with acquired drug resistance (often multi-factorial) can be made responsive to drugs again by combining the drug treatment with heat.
引用
收藏
页码:191 / 196
页数:6
相关论文
共 22 条
[1]  
[Anonymous], 1995, THERMORADIOTHERAPY T
[2]   ARRHENIUS RELATIONSHIPS FROM THE MOLECULE AND CELL TO THE CLINIC [J].
DEWEY, WC .
INTERNATIONAL JOURNAL OF HYPERTHERMIA, 1994, 10 (04) :457-483
[3]  
DEWEY WC, 1978, CANC THERAPY HYPERTH, P149
[4]  
Dewhirst M.W., 2003, CANC MED, P623
[5]   MOLECULAR CHAPERONES [J].
ELLIS, RJ ;
VANDERVIES, SM .
ANNUAL REVIEW OF BIOCHEMISTRY, 1991, 60 :321-347
[6]   HYPERTHERMIC POTENTIATION OF CISPLATIN TOXICITY IN A HUMAN SMALL-CELL LUNG-CARCINOMA CELL-LINE AND A CISPLATIN-RESISTANT SUBLINE [J].
HETTINGA, JVE ;
LEMSTRA, W ;
MEIJER, C ;
MULDER, NH ;
KONINGS, AWT ;
DEVRIES, EGE ;
KAMPINGA, HH .
INTERNATIONAL JOURNAL OF HYPERTHERMIA, 1994, 10 (06) :795-805
[7]   Reduction of cellular cisplatin resistance by hyperthermia - a review [J].
Hettinga, JVE ;
Konings, AWT ;
Kampinga, HH .
INTERNATIONAL JOURNAL OF HYPERTHERMIA, 1997, 13 (05) :439-457
[8]   THE RELATIONSHIP OF INCREASED NUCLEAR-PROTEIN CONTENT INDUCED BY HYPERTHERMIA TO KILLING OF HELA S3 CELLS [J].
KAMPINGA, HH ;
TURKELUYGUR, N ;
ROTI, JLR ;
KONINGS, AWT .
RADIATION RESEARCH, 1989, 117 (03) :511-522
[9]   Mechanism of radiosensitization by hyperthermia (≥43°C) as derived from studies with DNA repair defective mutant cell lines [J].
Kampinga, HH ;
Dynlacht, JR ;
Dikomey, E .
INTERNATIONAL JOURNAL OF HYPERTHERMIA, 2004, 20 (02) :131-139
[10]   Hyperthermic radiosensitization: mode of action and clinical relevance [J].
Kampinga, HH ;
Dikomey, E .
INTERNATIONAL JOURNAL OF RADIATION BIOLOGY, 2001, 77 (04) :399-408