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塞替派诱发人支气管上皮恶性转化成瘤细胞的染色体畸变
引用本文:周喆,袁素波,郭巧珍,廖明阳. 塞替派诱发人支气管上皮恶性转化成瘤细胞的染色体畸变[J]. 中国药理学与毒理学杂志, 2002, 16(4): 302-305
作者姓名:周喆  袁素波  郭巧珍  廖明阳
作者单位:军事医学科学院毒物药物研究所,北京,100850
摘    要:目的 旨在了解转化细胞在成瘤过程中的细胞遗传学改变。方法 运用染色体G显带技术研究永生化人支气管上皮细胞 (BEAS 2B)恶性转化后的裸小鼠接种成瘤细胞 (BEAS TT)的染色体畸变。结果 瘤细胞在传代早期基本以近二倍体细胞为主 ,随着细胞代龄的增加 ,各肿瘤细胞系的细胞染色体数目变化趋势不同 ,其中BEAS TTa逐渐形成以多倍体细胞为主的细胞群 ,而BEAS TTb ,BEAS TTc则以近二倍体细胞为主份额细胞。核型分析表明 3个瘤细胞系的核型与BEAS TE不同 ,在其基础上有新的染色体 (14号染色体 )丢失和标记染色体 (M4 )的增加。结论 细胞染色体数目不稳定 ,14号染色体的丢失和M4染色体的增加 ,可能与BEAS TE的裸小鼠成瘤性有关

关 键 词:塞替派  上皮细胞,支气管,人  转化,恶性  染色体
收稿时间:2001-11-21

Chromosome aberration of tumorigenic human bronchial epithelial cells induced by thiotepa
ZHOU Zhe, YUAN Su-Bo, GUO Qiao-Zhen, LIAO Ming-Yang. Chromosome aberration of tumorigenic human bronchial epithelial cells induced by thiotepa[J]. Chinese Journal of Pharmacology and Toxicology, 2002, 16(4): 302-305
Authors:ZHOU Zhe   YUAN Su-Bo   GUO Qiao-Zhen   LIAO Ming-Yang
Affiliation:(Institute of Pharmacology and Toxicology, Academy of Military Medical Sciences, Beijing 100850, China)
Abstract:AIM To analyze cytogenetical changes in transformed cells in tumorigenesis. METHODS G-banding technique was used to analyze the karyotype of BEAS-TTs. BEAS- TTa, BEAS-TTb and BEAS-TTc are tumor cells derived from subcutaneously implanted malignantly transformed immortalized non-tumorigenic human bronchial epithelial cells by thiotepa (BEAS-TE) in nude mice. RESULTS The modal chromosomal number of three tumor cells was near diploid at passage 7, 6, 6 for tumor cell BEAS-TTa, BEAS-TTb and BEAS-TTc, respectively. Proceeding with subcultures, there was a shift for BEAS-TTa from near diploid toward poly-ploid at passage 27,the proportion of poly- ploid cells was up to 96%, while the BEAS-TTb and BEAS-TTc were maintained near diploid. On the chromosomal basis of BEAS-2B and BEAS-TE,BEAS-TT contin ued to loss the chromosome 14 and showed a new abnormal chromosome, the marker 4. CONCLUSION The progressive chromosomal changes that occurred during tumorigenesis process in nude mice was significantly related to BEAS-TE acquisition of strong tumorigenicity in nude mice.
Keywords:thiotepa  epithelial cells  bronchial  human  transformation  malignant  chromosome
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