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基于八腔室玻片的染色体畸变初筛方法的建立与验证 被引量:2

Establishment and validation of a chromosomal aberration screening test using eight-well chamber slides
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摘要 目的:为简化传统体外染色体畸变试验工序并减少受试物用量,建立基于八腔室玻片的染色体畸变初筛方法。方法:首先利用环磷酰胺(CP)和丝裂霉素C(MMC)作为阳性模式药物,分别建立CP作用6 h(+S_9)和MMC作用24 h(-S_9)的八腔室玻片的染色体畸变试验方法。再用于检测5个已知遗传毒性物质苯并芘[B(a)P]、2-氨基蒽(2-AA)、甲基磺酸甲酯(MMS)、乙基磺酸甲酯(EMS)、依托泊苷(Eto)和2个非遗传毒性药物氨苄青霉素钠(AS)和氯化钠(SC)在±S_9两个条件下的染色体畸变效应,验证该法的灵敏度和特异性。结果:CP和MMC分别在±S_9活化系统中染色体结构畸变率呈浓度依赖性增加,与溶剂对照组相比,差异均具有统计学意义(P<0.05或P<0.01)。在验证试验中,B(a)P和2-AA在+S_9系统中呈染色体畸变阳性,与溶剂对照组相比,差异均具有统计学意义(P<0.05或P<0.01);MMS、EMS和Eto的染色体畸变率呈浓度依赖性增加(±S_9结果均为阳性),与溶剂对照组相比,差异均具有统计学意义(P<0.05或P<0.01);而2个已知非遗传毒性药物(AS和SC)在±S_9系统中均呈阴性结果。结论:通过上述物质的验证表明,八腔室玻片染色体畸变试验是一种简单、快速、有效的遗传毒性初筛方法。 OBJECTIVE:A chromosomal aberration(CA) screening test was established using eight-well chamber slides without adopting complicated procedures and chemical agents in the traditional chromosomal aberration test in vitro.The validation of the protocol was conducted using several genotoxic chemicals with various mechanisms of action and non-genotoxic compounds.METHODS:Optimized conditions for the test procedure in which cells were treated with cyclophosphamide(CP) for 6 h(for the +S_9 condition) and mitomycin C(MMC) for 24 h(for the -S_9 condition) were investigated.And then five known genotoxic chemicals including benzo(a)pyrene[B(a)P],2-aminoanthracene(2- AA),methyl methanesulphonate(MMS),ethyl methansulfonate(EMS),etoposide(Eto) and two non-genotoxic chemicals including ampicilin sodium salt(AS) and sodium chloride(SC) were used in the sensitive and specific validation research under these conditions.RESULTS:The CA percentage of CP(6 h,+S_9) and MMC(24 h,-S_9) showed dose-dependent accumulation.In the validation tests,B(a)P and 2-AA were positive only in(6 h,+S_9) condition while MMS,EMS and Eto showed positive results in both +/-S_9 conditions.AS and SC were negative in both +/-S_9 conditions.CONCLUSION: The chromosomal aberration test using eight-well chamber slides could be considered as a simple,rapid and effective method,which could be used in genotoxicity screening in the early research phase of drug development.
出处 《癌变.畸变.突变》 CAS CSCD 2011年第4期250-254,共5页 Carcinogenesis,Teratogenesis & Mutagenesis
基金 国家上海科委专业技术服务能力建设基金项目(09DZ2290900)
关键词 八腔室玻片 染色体畸变 初筛方法 eight-well chamber slide chromosomal aberration screening
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参考文献14

  • 1Bolognesi C. Genotoxicity of pesticides: a review of human biomonitoring studies[J]. Mutat Res, 2003, 543 (3): 251-272.
  • 2Albertini R J, Anderson D, Douglas GR, et al. IPCS guidelines for the monitoring of genotoxie effects of carcinogens in human[J]. Mutat Res, 2000, 463 (2): 111-172.
  • 3Natarajan AT. Chromosome aberrations: past, present and future[J]. MutatRes, 2002, 504(1/2): 3-16.
  • 4Organization for Economic Cooperation and Development (OECD). Guideline for the testing of chemicals: in vitro mammalian chromosome aberration test[S]. Paris : OECD, 1997 : 473.
  • 5Yamamoto M, Motegi A, Seki J. The optimized conditions for the in vitro micronucleus (MN) test procedures using chamber slides[J]. Environ Mutagen Res, 2005, 27(3): 145-151.
  • 6Fomina J, Darroudi F, Boei JJWA, et al. Discrimination between complete and incomplete chromosome exchanges in Xirradiated human lymphocytes using FISH with pancentromeric and chromosome specific DNA probes in combination with telomeric PNA probe[J]. Int J Radiat Biol, 2000, 76 (6): 817-823.
  • 7Kirsch-Volders M, Sofuni T, Aardema M, et al. Report from the in vitro micronucleus assay working group[J]. Mutat Res, 2003, 540 (2): 153-163.
  • 8李睿,熊义,陈虹颖,郑从义,屈三甫.丝裂霉素诱导CHO-K1细胞凋亡及对其细胞周期的影响[J].武汉大学学报(理学版),2004,50(2):251-255. 被引量:1
  • 9王新禹,梁前进.环磷酰胺的毒副作用机制及应对措施[J].药学进展,2006,30(10):452-456. 被引量:41
  • 10Phelps JB, Garriott ML, Hoffman WP. A protocol for the in vitro micronucleus test II: Contributions to the validation of a protocol suitable for regulatory submissions from an examination of 10 chemicals with different mechanisms of action and different levels of activity [J]. Mutat Res, 2002, 521 (1/2) : 103-112.

二级参考文献17

  • 1仪慧兰,秦海峰,李红孩.环磷酰胺诱发蚕豆体细胞遗传损伤的研究[J].植物研究,2004,24(4):439-442. 被引量:8
  • 2肖凯,李宏霞.环磷酰胺剂量、取样时间对小鼠骨髓微核率的影响[J].癌变.畸变.突变,2005,17(6):367-369. 被引量:13
  • 3周友珍,陈惠祯,杨庆忆,刘诗权,侯汉英.人卵巢癌顺铂耐药细胞株的建立及其耐药机制的研究[J].中华医学杂志,1996,76(9):680-683. 被引量:27
  • 4Liou Saou-hsing,Chen Yeong-hwang,Loh Ching-hui,et al. The Association Between Frequencies of Mitomycin C-induced Sister Chromatid Exchange and Cancer Risk in Arseniasis[J]. Toxicology Letters,2002,129(3):237-243.
  • 5Sambrook J,Russel W. Molecular Cloning a Laboratory Manual.3rd ed[M]. New York:Cold Spring Harbor Laboratorg Press,2002.
  • 6Tolskaya E,Romanova L,Kolesnikova M,et al.Apoptosis-Inducing and Apotosis-Preventing Functions of Poliovirus[J]. J Virol,1995,69:1181-1189.
  • 7Niocoletci I.A Rapid and Simple Method for Meaeuring Thymocyte Apoptosis by Propidum Iodidle Staining and Flow Cytometry [J].J Imm Neth,1991,139:271-280.
  • 8Salwa Abid-Essefi, Isabelle Baudrimont, Wafa Hassen,et al.DNA Fragmentation,Apoptosis and Cell Cycle Arrest Induced by Zearalenone in Cultured DOK, Vero and Caco-2 Cells:Prevention by Vitamin E[J].Toxicology,2003,192:237-248.
  • 9Feng Liang,Chengtai Wu, Huakuan Lin. Coppre Compex of Hydroxyl-Substituted Triazamacrocyclic Ligand and Antitumor Activity[J].Bioorganic & Medicinal Chemistry Letter,2003,13:2469-2472.
  • 10郑从义,屈三甫,胡国斌.血液肿瘤细胞凋亡形态学观察的改良荧光染色法[J].肿瘤防治研究,1998,25(6):432-433. 被引量:18

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