Effects of culture temperatures on radio- and thermosensitivity of human cancer cells.
Effects of culture temperatures on radio- and thermosensitivity of human cancer cells.
批准号:
62570470
负责人:
NAKATSUGAWA Shigekazu
金额:
$1.47万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for General Scientific Research (C)
财政年份:
1987
资助国家:
日本
项目状态:
已结题
起止时间:
1987 至 1989
中文摘要
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英文摘要
So far, most of the characteristics of cancer cells have been investigated through culturing at 37.0゚C. However, 37.0゚C is not always optimal temperature for the growth of cells or repairing damage induced by radiation or hyperthermia. In the treatment for cancer by radiation and other modalities, on the other hand, local control is one of the main purpose, in relevance to cell death. Another purpose pf the therapy may be the prevention and treatment of metastasis. So far, very few metastasis. models derived from human malignancies have been available. As for human lung cancer xenograft, both hematogenous and lymphatogenic route of metastasis has been observed in only one report. In this study, various radio- biological parameters of AOI cells, a cell line derived from human lung cancer, were examined at various culture temperatures, that is 35.0, 36.0, 37.0, 38.0 39.0゚C. Culture temperatures showed apparent influences on growth rate, cell density in the plateau phase, thermosensitivit … More ies and Elkind-Sutton type recovery in AOI cells. At 37.0゚C, X-ray survival curve in a semilogarithmic graph increased its slope as the doses increased. Moreover, feeder layer AOI cells (1.0- 20x 10^4/6cm petri dish) which were irradiated with 25Gy of X-rays showed a potent cytotoxicities on intact AOI cells at 37.0゚C. At 35.0゚C, the cytotoxicity of feeder layer was ten times as much as at 37.0゚C, while at 39.0゚C it was one tenth as much as at 37.0゚C. Conditioned media from the feeder layer did show a potent cytotoxic effects on intact AOI cells, irrespective of culture temperatures. So far, feeder layer has been regarded as a growth stimulant. In AOI cells, some toxic substances may be excreted from heavily X-irradiated cells. This cytotoxicity may not be attributed to chromosome aberrations induced by X-rays.When AOI tumors intradermally inoculated into hind legs of KSN nude mice reached 2.5cm in diameter, spontaneous multiple metastases were observed in 100% of the mice. The site of metastases included spleen, lung, kidney, liver and adrenal gland other than lymphnodes of various areas. Each metastatic foci were investigated both macroscopically and microscopically. ^<31>P spectra of AOI tumors were also investigated with MRS (BEM, 2T) after local X-irradiation and or hyperthermia. This system may be very useful for the study on both local control and metastasis of cancer. Less
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中津川重一: "潜在的致死損傷からの回復阻害剤" 医学のあゆみ. 150. 947-952 (1989)
Shigekazu Nakatsukawa:“潜在致命伤害恢复的抑制剂”《医学史》150. 947-952 (1989)。
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河野寛一: "悪性神経膠腫のACNU、増感剤併用照射療法の試み" 脳神経. 41. 1071-1075 (1989)
Hirokazu Kono:“ACNU 治疗恶性神经胶质瘤,与敏化剂联合放射治疗的试验”《颅神经病学》41. 1071-1075 (1989)。
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中津川重一: "PLD回復修飾因子について--ヒト癌細胞におけるPLD回復と修飾(2)--" 日本医学放射線学会生物部会試. 1. 12-15 (1988)
Shigekazu Nakatsukawa:“关于PLD恢复修饰剂--人癌细胞中的PLD恢复和修饰(2)-”日本医学放射学会生物学小组委员会试验1. 12-15(1988)。
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Eiji kidoya: "Influence of convection on temperature distribution in a dynamic phantom during RF capacitive heating." Hyperthermic Oncology,1988.1. 688-690 (1988)
Eiji Kidoya:“射频电容加热过程中对流对动态体模温度分布的影响。”
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Hirokazu Kouno, et al: "A trial of ACNU and radiation therapy with sensitizing agents for malignant gliomas." Central Nervous System. 41, 1071-1075, 1989.
Hirokazu Kouno 等人:“ACNU 和使用致敏剂进行放射治疗治疗恶性神经胶质瘤的试验。”
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