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作 者:曹波[1]
出 处:《中国优生与遗传杂志》2014年第6期28-30,F0004,共4页Chinese Journal of Birth Health & Heredity
摘 要:目的探讨染色体着丝粒点(Cd)的变异与AN3CA细胞和BMDC1细胞染色体非整倍性畸变的关系。方法肿瘤细胞株传代后用常规方法制备染色体,用直接法制备胚胎绒毛组织染色体标本,采用Cd-NOR同步银染分析技术研究AN3CA细胞和BMDC1细胞染色体Cd的变异。结果 1.AN3CA细胞染色体Cd缺失率为1.87%、Cd迟滞复制率为0.19%、小Cd率为1.52%、Cd-NOR融合率为1.88%、与正常人胚胎绒毛细胞染色体Cd相比较,AN3CA细胞染色体Cd缺失、Cd-NOR融合显著升高(P<0.0125),而小Cd、Cd迟滞复制其差异无统计学意义。2.BMDC1细胞染色体Cd缺失率为1.13%、Cd迟滞复制率为1.52%、小Cd率为1.53%、Cd-NOR融合率为0.57%、与正常人胚胎绒毛细胞染色体Cd相比较,BMDC1细胞染色体Cd缺失、Cd迟滞复制显著升高(P<0.0125),而小Cd、Cd-NOR融合其差异无统计学意义。结论 1.AN3CA细胞染色体非整倍性畸变可能主要源于Cd缺失、Cd-NOR融合;2.BMDC1细胞染色体非整倍性畸变可能主要源于Cd缺失、Cd迟滞复制。Objective: To study the relation between the centromeric dots (Cd) variation of AN3CA cells and BMDC1 cells and the chromosome aneuploidy aberration. Methods: Chromosome of tumor cells were done with general method, Chromosome of normal embryonic villi were done straightly. A Cd-NOR in-phase argentum dye analysis technique modified by this laboratory was used to study centromeric dots (Cd) variation of AN3CA cells and BMDC 1 cells. Results: 1. Frequency of Cd loss in AN3CA cells was 1.87%, Frequency of Cd duplication laggard was 0.19%, Frequency of little Cd was 1.52%, Frequency of Cd-NOR amalgamation was 1.88%. Frequency of Cd loss and Cd-NOR amalgamation in AN3CA cells were significantly higher than those of normal embryonic villi (P〈0.0125) . Frequency of Cd duplication laggard and little Cd showed no difference between AN3CA cells and normal embryonic villi cells. 2. Frequency of Cd loss in BMDC1 cells was 1.13%, Frequency of Cd duplication laggard was 1.52%, Frequency of little Cd was 1.53%, Frequency of Cd-NOR amalgamation was 0.57%. Frequency of Cd loss, Cd duplication laggard in BMDC 1 cells were significantly higher than those of normal embryonic villi cells (P〈0.0125) . Frequency of little Cd, Cd-NOR amalgamation showed no difference between BMDC1 cells and normal embryonic villi. Conclusion: 1.Cd loss and Cd-NOR amalgamation might be related with aneuploidy aberration of AN3CA cells. 2.Cd loss and Cd duplication laggard might be related with aneuploidy aberration of BMDC 1 cells.
分 类 号:R394.2[医药卫生—医学遗传学]
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