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^(60)C0γ射线诱发人支气管上皮细胞恶性转化模型的建立 被引量:3

^(60)Coγ-ray irradiation induced malignant transformation model of human bronchus epithelium cell
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摘要 目的:建立γ射线辐射诱导支气管上皮细胞恶性转化模型。方法:永生化人支气管上皮细胞BEAS-2B经总剂量22 Gy ^(60)Coγ射线分3次照射后进行传代培养,应用平板克隆实验、血清抗性实验、细胞软琼脂集落实验检测该细胞系恶性程度;裸鼠皮下种植辐射细胞检测其成瘤能力,成瘤组织H-E染色及免疫组化进行病理学观察。结果:(1)平板克隆实验表明照射细胞培养至35代后其增殖能力明显增加(P<0.05或P<0.01),血清抗性实验显示照射组细胞在第45代后克隆形成增加(P<0.01),而在照射后50代细胞软琼脂集落的形成能力明显增加(P<0.01),显示BEAS-2B细胞经辐射后出现了恶性转化。(2)皮下种植22 Gy 50代细胞的8只裸鼠50 d后1只成瘤,种植22 Gy 60代辐射细胞的8只裸鼠中有4只成瘤;成瘤组织病理检测及免疫组化证实为上皮细胞癌。结论:成功地建立了^(60)Coγ射线诱导的支气管上皮细胞恶性转化模型。 Objective : To establish a malignant transformation model of human bronchus epithelium cells (BEAS-2B) by ^60Co γ-ray irradiation. Methods: Immortalized BEAS-2B cells were subjected to a irradiation with ^60Co γ-ray for three times, with a total dose of 22 Gy. Then the cells were cultured and subjected to colony-forming test, serum antibody experiment, and colony formation experiment in soft agar to detect the level of cellular malignant transformation. Nude mice were implanted subcutaneously with radiated cells to examine the tumor-forming ability of the irradiated cells; the formed tumor tissues were stained with H-E and immunohistochemistry methods for pathology observation. Results: (1) Colonyforming test showed that the proliferation ability of the cells was significantly increased after the 35th passage after 22 Gy radiation (P 〈0.05 or P 〈0.01 ) ; serum antibody experiment demonstrated that the colony forming ability was increased at the 45th passage after irradiation(P 〈0.01 ) ; and in the soft agar colony formaing experiment, colony forming ability of the 50th passage cells was increased significantly(P 〈0.01 ). All the above 3 test indicated the malignant transformation of BEAS-2B cells after irradiation. (2) Eight nude mice were implanted with the 50th passage cells after irradiation, and one mice had tumor formed at the nape 50 days after implantation; another 8 nude mice were implanted with 60th passage cells and 4 mice had tumor formed. Pathological observation indicated the formed tumor was epithelial cell carcinoma. Conclusion: We have successfully established the malignant transformation model of human bronchus epithelium cells (BEAS-2B) by ^60Co γ-ray irradiation.
出处 《中国肿瘤生物治疗杂志》 CAS CSCD 2007年第5期435-439,共5页 Chinese Journal of Cancer Biotherapy
基金 国家自然科学基金(No.30370359) Supported by the National Natural Science Foundation of China(No.30370359)
关键词 辐射 恶性转化 人支气管上皮细胞 上皮细胞癌 irradiation malignant transformation human bronchus epithelium cell (BEAS-2B) epithelial cell
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  • 1赵永成,王继先,张卫,李本孝,樊体强,张景源.我国医用诊断X射线工作者1950—1995年肿瘤死亡危险分析[J].中华放射医学与防护杂志,2002,22(4):243-245. 被引量:11
  • 2王玉民.我国辐射致癌基础实验研究成果概述[J].山西医药杂志,1999,28(2):91-97. 被引量:2
  • 3韩玲,蔡建明,李百龙,黄定德,黄越承,赵芳,孙顶,傅志超,陈杞.^(60)Coγ射线照射诱发小鼠恶性肿瘤[J].第二军医大学学报,2003,24(7):745-748. 被引量:22
  • 4Yang TC, Georgy KA, Craise LM, et al. Initiation of oncogenic transformation in human mammary epithelial cells by charged particles[J]. Radiat Oncol Investig, 1997, 5(3) : 134-138.
  • 5Hei TK, Zhao YL, Roy D, et al. Molecular alterations in tumorigenic human bronchial and breast epithelial cells induced by high LET radiation [J]. Adv Space Res, 2001,27(2) :411-419.
  • 6Yamada S, Yang TC, George K, et al. Microsatellite instability in human mammary epithelial cells transformed by heavy ions [ J ]. Adv Space Res, 1998,22 (12) : 1709-1717.
  • 7Roti JL, Malyapa RS, Bisht KS, et al. Neoplastic transformation in C3H 10T(1/2) cells after exposure to 835.62 MHz FDMA and 847, 74 MHz CDMA radiations[J]. Radiat Res, 2001, 155( 1 ) : 239-247.
  • 8Rhim JS, Thraves P, Dfitschilo A, et al. Radiation-induced neoplastic transformation of human cells [ J ]. Scanning Microsc, 1993,7( 1 ) :209-215.
  • 9Hei TK, Piao CQ, Willey JC,et al. Malignant transformation of human bronchial epithelial cells by random-simulated α-particles[ J ]. Carcinogenesis, 1994, 15 (3) : 431-437.
  • 10葛世丽,楼铁柱,项晓琼,陈伟,吴德昌.α粒子照射诱发BEP2D细胞恶性转化模型的建立[J].癌症,2001,20(9):901-905. 被引量:21

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  • 1Ying W, Zhang K, Qian X, et al. Proteome analysis on an early transformed human bronchial epithelial cell line, BEP2D, after alpha-particle irradiation [J]. Proteomics, 2003, 3(1):64-72.
  • 2Joseph S, David W R. Molecular Cloing: A Laboratory Manual [M]. Third edition. New York: Cold Spring Harbor Laboratory Press, 1713-1726.
  • 3Shihuya M. Molecular mechanism of carcinogenesis [J]. Gan To Kagaku Ryoho, 1993,20 ( 5 ) : 677-683.
  • 4Demura Y, Ameshima S, Ishizaki T, et al. Glutathione peroxidase [J].Nippon Rinsho, 1999,57 (Suppl) : 448-450.
  • 5Doroshow J H, Akman S, Chu F F, et al. Role of the glutathione-glutathione peroxidase cycle in the cytotoxicity of the anticancer quinones [J]. Pharmacol Ther, 1990,47 (3):359- 370.
  • 6Finley J W, Davis C D. Selenium (Se) from high-selenium broccoli is utilized differently than selenite, selenate and selenomethionine, but is more effective in inhibiting colon carcinogenesis [J]. Biofactors, 2001,14(1-4) : 191-196.
  • 7Spallholz J E. Selenium and glutathione peroxidase: essential nutrient and antioxidant component of the immune system [J]. Adv Exp Med Biol, 1990,262: 145-158.
  • 8Michelson A M. Selenium glutathione peroxidase: some aspects in man [J]. J Environ Pathol Toxicol Oncol, 1998, 17(3-4): 233-239.
  • 9Jefferies S, Kote-Jarai Z, Goldgar D, et al. Association between polymorphisms of the GPX1 gene and second primary tumours after index squamous cell cancer of the head and neck [J]. Oral Oncol, 2005,41 (5) : 455-461.
  • 10Ichimura Y, Habuchi T, Tsuchiya N, et al. Increased risk of bladder cancer associated with a glutathione peroxidase 1 codon 198 variant [J]. J Urol, 2004,172(2) :728-732.

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