Growth suppression of four cancer cells by hyperbaric nitrous oxide and methotrexate

被引:1
作者
Jung, Cheol Hee [1 ]
Sim, Ji Yeon [2 ]
Ahn, Wonsik [1 ]
机构
[1] Univ Ulsan, Seoul Natl Univ Hosp, Dept Anesthesiol & Pain Med, Seoul, South Korea
[2] Univ Ulsan, Coll Med, Seoul, South Korea
关键词
Methotrexate; Nitrous oxide; Tumor growth suppression;
D O I
10.4097/kjae.2010.58.1.61
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Background: Nitrous oxide concentration is easily controlled by respiratory ventilation. It suppresses bone marrow via the inhibition of thymidylate synthesis. The aim of this work was to determine the optimal pressure and exposure duration of nitrous oxide, as well as methotrexate concentration that maximizes the suppression of 4 cancer cells: CCRF-CEM, K562, A549 and MDA-MB-231. Methods: Each cancer cell was cultured in a hyperbaric chamber at 1, 2 and 3 atmosphere of 74% nitrous oxide for 24, 48, and 72 hours at 0, 0.3, 0.7, 1, 2, 5 and 10 mu M methotrexate (MTX), respectively. The results were expressed in the ratio of the number of cancer cells cultured under specific conditions (S cells) to that under normal conditions (N cells). Results: The S/N ratio of CCRF-CEM cells was 87.4% in 24-hour culture, 95.0% in 48-hour culture and 115.9% in 72-hour culture (P < 0.05). The S/N ratio of K562 cells was 103.6% at 1 atm, 102.4% at 2 atm and 115.6% at 3 atm (P < 0.05). The S/N ratio of A549 cells was 94.3% at 1 atm, 94.1% at 2 atm, 99.3% at 3 atm, 96.2% in 24-hour culture, 99.2% in 48-hour culture and 99.3% in 72-hour culture (P > 0.05). However, the S/N ratio of MDA-MB 231 cells was 66.9% in 24-hour culture, 83.1% in 48 hour culture and 87.8% in 72-hour culture (P < 0.05). Conclusions: Only the growth of the MDA-MB-231 cells was significantly reduced after a longer exposure time to nitrous oxide, but those of the other cells were not.
引用
收藏
页码:61 / 69
页数:9
相关论文
共 20 条
[1]  
Baum Jan A, 2004, Curr Opin Anaesthesiol, V17, P513, DOI 10.1097/00001503-200412000-00012
[2]   When nitrous oxide is no laughing matter: nitrous oxide and pediatric anesthesia [J].
Baum, Victor C. .
PEDIATRIC ANESTHESIA, 2007, 17 (09) :824-830
[3]   Lesson of the week - Toxicity after intermittent inhalation of nitrous oxide for analgesia [J].
Doran, M ;
Rassam, SS ;
Jones, LM ;
Underhill, S .
BRITISH MEDICAL JOURNAL, 2004, 328 (7452) :1364-1365
[4]   EFFECT OF NITROUS-OXIDE AND METHOTREXATE ON FOLATE COENZYME POOLS OF BLAST CELLS FROM LEUKEMIA PATIENTS [J].
ERMENS, AAM ;
SCHOESTER, M ;
LINDEMANS, J ;
ABELS, J .
LEUKEMIA RESEARCH, 1991, 15 (2-3) :165-171
[5]  
Fiskerstrand T, 1997, J PHARMACOL EXP THER, V282, P1305
[6]   Optimisation and molecular signalling of apoptosis in sequential cryotherapy and chemotherapy combination in human A549 lung cancer xenografts in SCID mice [J].
Forest, V. ;
Hadjeres, R. ;
Bertrand, R. ;
Jean-Francois, R. .
BRITISH JOURNAL OF CANCER, 2009, 100 (12) :1896-1902
[7]   Benefit of a combined treatment of cryotherapy and chemotherapy on tumour growth and late cryo-induced angiogenesis in a non-small-cell lung cancer model [J].
Forest, Valerie ;
Peoc'h, Michel ;
Campos, Lydia ;
Guyotat, Denis ;
Vergnon, Jean-Michel .
LUNG CANCER, 2006, 54 (01) :79-86
[8]  
안원식, 2006, Korean Journal of Anesthesiology, V50, P308
[9]   NITROUS-OXIDE - A CAUSE OF CANCER OR CHEMOTHERAPEUTIC ADJUVANT [J].
KOBLIN, DD .
SEMINARS IN SURGICAL ONCOLOGY, 1990, 6 (03) :141-147
[10]   NITROUS-OXIDE HAS MULTIPLE DELETERIOUS EFFECTS ON COBALAMIN METABOLISM AND CAUSES DECREASES IN ACTIVITIES OF BOTH MAMMALIAN COBALAMIN-DEPENDENT ENZYMES IN RATS [J].
KONDO, H ;
OSBORNE, ML ;
KOLHOUSE, JF ;
BINDER, MJ ;
PODELL, ER ;
UTLEY, CS ;
ABRAMS, RS ;
ALLEN, RH .
JOURNAL OF CLINICAL INVESTIGATION, 1981, 67 (05) :1270-1283