Analysis of Thermotolerance of Cancer by Introduction of Oncogeges
通过引入癌基因来分析癌症的耐热性
基本信息
- 批准号:07671015
- 负责人:
- 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 Scientific Research (C)
- 财政年份:1995
- 资助国家:日本
- 起止时间:1995 至 1996
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Hyperthermia is introduced as a new modality of cancer treatment. As thermosensitivity varies to tumors in ten times, all tumors can not be applied to hyperthermia. Oncogenesis of cells is induced by expression of mutated oncogenes. We introduced oncogenes to normal cells and obtained transformed cells, and examined thermosensitivity of cells, analyzing oncogenes which determine thermosensitivity. This study will predict results of cancer treatment by hyperthermia before its treatment, and most effective treatment would be selected.In this study, mouse cultured cells, NIH3T3, were used for normal cells. Following oncogenes were introduced to normal cells and obtained transformed cells : myc, Ki-ras, N-ras, H-ras, int-2, fgr, sis, and src.Thermosensitivity of transformed cells as well as normal cells to 44゚C was examined. The transformed cells by Ki-ras showed resistant to hyperthermia. This means that tumors induced by Ki-ras is not desirable to treat by hyperthermia.Thermotolerance induced by the treatment of 44゚C,for 15 min was examined for above transformed cells. The thermotolerant ratio analyzed at 4 hour-interval was 2.06 for transformed cells by Ha-ras which was the smallest in examined cells. This means that tumors induced by Ha-ras is desirable to treat by fractionated hyperthermia.
热疗作为一种新的癌症治疗方式被引入。由于肿瘤的热敏感性相差十倍,因此不能对所有肿瘤进行热疗。细胞的肿瘤发生由突变的癌基因的表达诱导。我们将癌基因导入正常细胞并获得转化细胞,并检查细胞的热敏性,分析决定热敏性的癌基因。本研究将在治疗前预测热疗治疗癌症的效果,并选择最有效的治疗方法。在本研究中,小鼠培养细胞NIH 3 T3被用作正常细胞。将myc、Ki-ras、N-ras、H-ras、int-2、fgr、sis和src等癌基因导入正常细胞,获得转化细胞,并检测转化细胞和正常细胞对44 ℃的温度敏感性。Ki-ras基因转化的细胞对高温有抵抗作用。用44 ℃处理上述转化细胞15分钟,观察其耐热性。Ha-ras转化细胞每隔4小时分析的耐热率为2.06,这是受检细胞中最小的。这意味着由Ha-ras诱导的肿瘤需要通过分次热疗来治疗。
项目成果
期刊论文数量(21)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
K.Komatsu et al: "The scid factor on human chromosome 8 restores V (D) J recombination in addition to double-strand break repair" Cancer Res. 55. 1774-1779 (1995)
K.Komatsu 等人:“除了双链断裂修复之外,人类 8 号染色体上的 scid 因子还能恢复 V (D) J 重组”Cancer Res。
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
- 作者:
- 通讯作者:
T.Matsuo: "Inhibition of epidermal growth factor binding system by ionizing radiation in A431 human squamous carcinoma cells." Cancer Letters. 89. 153-159 (1995)
T.Matsuo:“电离辐射对 A431 人鳞状癌细胞中表皮生长因子结合系统的抑制。”
- DOI:
- 发表时间:
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- 影响因子:0
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- 通讯作者:
N.Sadamori: "Incidence of intracranial meningiomas in Nagasaki atomic-bomb survivors" Int.J.Cancer. 67. 318-322 (1996)
N.Sadamori:“长崎原子弹幸存者颅内脑膜瘤的发病率”Int.J.Cancer。
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
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- 通讯作者:
M.Ihara et al: "Thermosensitivity and DNA-PK activity fibroblast cells derived from scid mouse containing fragment of human 8 chromosome" Nagasaki Medical Journal. 71. 352-354 (1996)
M.Ihara 等人:“含有人类 8 号染色体片段的 scid 小鼠成纤维细胞的热敏感性和 DNA-PK 活性”长崎医学杂志。
- DOI:
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- 影响因子:0
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- 通讯作者:
H.Kondo: "Statistical associations between radiation exposure and the clinical examination data of Japanese radiology technicalans." J.Epidemiol. 5(2). 51-57 (1995)
H.Kondo:“辐射暴露与日本放射学技术人员的临床检查数据之间的统计关联。”
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- 影响因子:0
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OKUMURA Yutaka其他文献
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{{ truncateString('OKUMURA Yutaka', 18)}}的其他基金
Combined effects of light and naphthalene on marine microalgae
光和萘对海洋微藻的联合影响
- 批准号:
17510034 - 财政年份:2005
- 资助金额:
$ 1.47万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Radiosensitivity of Scid Cells Deficient in Repair of DNA Damages Induced by High LET Irradiation
高 LET 辐射诱导的 DNA 损伤修复缺陷的 Scid 细胞的放射敏感性
- 批准号:
12670885 - 财政年份:2000
- 资助金额:
$ 1.47万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Radiosensitivity of scid cells for heavy ion particles
scid细胞对重离子粒子的放射敏感性
- 批准号:
09670943 - 财政年份:1997
- 资助金额:
$ 1.47万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
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