Biological characteristics and genetic abnormalities in very, young patients with lung cancer (【less than or equal】30 years of age)
极年轻肺癌患者(【小于等于】30岁)的生物学特征及基因异常
基本信息
- 批准号:12670424
- 负责人:
- 金额:$ 1.92万
- 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:2000
- 资助国家:日本
- 起止时间:2000 至 2003
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Retrospectively, 20 patients with lung cancer aged【less than or equal】30 years from three Institutions were compared with 1848 patients of aged >30 years admitted to National Shikoku Cancer Center between 1981 and 2001. Median survival time (MST) and other factors were assessed using the Cox regression model and the chi-square test, respectively. In a multivariate analysis of the all population of lung cancer (n=1851), male gender, clinical symptoms, weight loss, a high LDH level, performance status (PS) of 【greater than or equal】2, and advanced-stage were independent negative prognostic factors. We found four patients with mucoepidermoid carcinoma among 20 patients of aged 【less than or equal】30 years. Mucoepidermoid carcinoma was excluded because of a high incidence (p<0.001) in the very young population, relatively early stage and longer survival time. The incidence of nonsmokers (p<0.001) and poorly differentiated non-small cell lung cancer (p=0.018) was also high in the very young … More group. In a multivariate analysis (n=16), clinical symptoms, LDH levels, and PS were also independent prognostic factors. There was no difference in survival between the young population and the general population. According to LDH levels and clinical symptoms, we classified the very young patients into three groups ; Group I : LDH (normal) and no clinical symptoms, Group II : LDH (normal) and clinical symptoms, and Group III : LDH (high) and clinical symptoms. The MST for group I, II and III were 50.0, 13.4, and 2.5 months, respectively (p=0.002). Excluding mucoepidermoid carcinoma, patients with a high LDH level and clinical symptoms showed poor prognosis in the very young population. Survival in the very young population was similar to that in the general population.We analyzed human lung cancer cell lines, SBC-3 and EBC-2 established in our laboratory. SBC-3 cells were derived from 24-year-old man with small-cell lung cancer, and EBC-2 cells from 20-year-old man with squamous cell carcinoma of the lung. SBC-3 cells showed heterozygous mutation codon 175 CGG to CAC (Arg to his) in Exon 5 of p58. EBC-2 showed desmosome and tonofilament be electron microscopy, and expressed drug resistant genes, MRP1, 3, 4, 5, and LRP, but LRP-2 and P-glycoprotein were not detected. Both SBC-3 and EBC-2 cells expressed CD34 by flow cytometry. Less
回顾性分析了1981年至2001年间,来自三个机构的20例年龄小于或等于30岁的肺癌患者与国立四国癌症中心收治的1848例年龄>30岁的肺癌患者。分别采用考克斯回归模型和卡方检验评估中位生存时间(MST)和其他因素。在对所有肺癌人群(n=1851)的多变量分析中,男性、临床症状、体重减轻、高LDH水平、体力状态(PS)[大于或等于]2和晚期是独立的阴性预后因素。我们在20例年龄小于或等于30岁的患者中发现了4例粘液表皮样癌。由于粘液表皮样癌在非常年轻的人群中发病率高(p<0.001),相对早期和生存时间较长,因此将其排除在外。非吸烟者(P<0.001)和低分化非小细胞肺癌(P=0.018)的发病率在非常年轻的人群中也很高 ...更多信息 组在多变量分析中(n=16),临床症状,LDH水平和PS也是独立的预后因素。年轻人和普通人的存活率没有差别。根据LDH水平和临床症状,我们将非常年轻的患者分为三组; I组:LDH(正常)和无临床症状,II组:LDH(正常)和临床症状,和III组:LDH(高)和临床症状。第I、II和III组的MST分别为50.0、13.4和2.5个月(p=0.002)。排除粘液表皮样癌,在非常年轻的人群中,LDH水平和临床症状高的患者预后差。我们分析了本实验室建立的人肺癌细胞系SBC-3和EBC-2。SBC-3细胞来源于患有小细胞肺癌的24岁男性,EBC-2细胞来源于患有肺鳞状细胞癌的20岁男性。SBC-3细胞p58基因外显子5密码子175 CGG → CAC(Arg → His)杂合突变。EBC-2细胞电镜下可见桥粒和张力丝,表达耐药基因MRP 1、3、4、5和LRP,但未检测到LRP-2和P-糖蛋白。流式细胞仪检测SBC-3和EBC-2细胞均表达CD 34。少
项目成果
期刊论文数量(34)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Kawai H, Kiura K.Tabata M., et al.: "Characterization of Non-Small-Cell lung Cancer Cell Lines Established before and after Chemotherapy"Lung Cancer. 35・3. 305-314 (2003)
Kawai H、Kiura K.Tabata M.等人:“化疗前后建立的非小细胞肺癌细胞系的表征”35・3(2003)。
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- 影响因子:0
- 作者:
- 通讯作者:
Y Segawa,H Ueoka, K Kiura, et al.: "A phase II study of cisplatin and 5-fluorouracil with concurrent hyperfractionated thoracic radiation for locally advanced non-small-cell lung cancer"British Journal of Cancer. 82・1. 104-111 (2000)
Y Sekawa、H Ueoka、K Kiura 等人:“顺铂和 5-氟尿嘧啶联合超分割胸部放射治疗局部晚期非小细胞肺癌的 II 期研究”,《英国癌症杂志》82・1。 -111 (2000)
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- 影响因子:0
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- 通讯作者:
Mimoto J., Kiura K, Matsuo K, et al.: "(-)-Epigallocatechin Gallate (EGCG) Can Prevent Cisplatin-Induced Lung Tumorigenesis in A/J Mice"Carcinogenesis. 81・4. 104-111 (2000)
Mimoto J.、Kiura K、Matsuo K 等:“(-)-表没食子儿茶素没食子酸酯 (EGCG) 可以预防 A/J 小鼠中顺铂诱导的肺肿瘤发生”81・4 (2000)。
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
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- 通讯作者:
Junko Mimoto,Katsuyuki Kiura,Mine Harada, et al.: "(-)-Epigallocatechin Gallate (EGCG) Can Prevent Cisplatin-Induced Lung Tumorigenesis in A/J Mice."Carcinogenesis. 21・5. 915-919 (2000)
Junko Mimoto、Katsuyuki Kiura、Mine Harada 等人:“(-)-表没食子儿茶素没食子酸酯 (EGCG) 可以预防 A/J 小鼠中顺铂诱导的肺肿瘤发生”。致癌作用 21・5。
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
- 作者:
- 通讯作者:
Kawai H, Kiura K, Tabata M., et al.: "Characterization of Non-Small-Cell Lung Cancer Cell Lines Established before an after Chemotherapy."Lung Cancer. 35・3. 305-314 (2002)
Kawai H、Kiura K、Tabata M. 等人:“化疗前后建立的非小细胞肺癌细胞系的特征”35・3 (2002)。
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- 影响因子:0
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KIURA Katsuyuki其他文献
KIURA Katsuyuki的其他文献
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{{ truncateString('KIURA Katsuyuki', 18)}}的其他基金
Basic study on combined modality therapy for advanced lung cancer harboring activated EGFR gene mutation
EGFR基因突变晚期肺癌联合治疗的基础研究
- 批准号:
25670399 - 财政年份:2013
- 资助金额:
$ 1.92万 - 项目类别:
Grant-in-Aid for Challenging Exploratory Research
Basic and clinical study of EGFR gene mutation-positive lung cancer using a genetically modified mouse
使用转基因小鼠进行EGFR基因突变阳性肺癌的基础和临床研究
- 批准号:
23390221 - 财政年份:2011
- 资助金额:
$ 1.92万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
A basic studyon malignant mesothelioma pathogenesis by internal radiation exposure of radium contained in the iron-containing protein
含铁蛋白镭内辐射照射恶性间皮瘤发病机制的基础研究
- 批准号:
23659432 - 财政年份:2011
- 资助金额:
$ 1.92万 - 项目类别:
Grant-in-Aid for Challenging Exploratory Research
Chemoprevention of Lung Cancer using Epidermal Growth Factor Receptor Transgenic Mice
使用表皮生长因子受体转基因小鼠化学预防肺癌
- 批准号:
19590895 - 财政年份:2007
- 资助金额:
$ 1.92万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Chemoprevention of second primary cancer in the patients with lung cancer
肺癌患者第二原发癌的化学预防
- 批准号:
16590746 - 财政年份:2004
- 资助金额:
$ 1.92万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
The Relationship between Mojor Histocompatibility Complex Class I Molccules and Natural Killer Cells
主要组织相容性复合物I类分子与自然杀伤细胞的关系
- 批准号:
08670519 - 财政年份:1996
- 资助金额:
$ 1.92万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
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