摘要
目的 探讨分析肝癌细胞的凋亡基因,并分析相应的基因序列,探讨三氧化二砷对肝癌细胞凋亡产生分子机制。方法 本次研究在实验时采用三氧化二砷对人肝癌HCC-9204细胞进行诱导凋亡,并采用抑制性消减杂交技术,对凋亡细胞中的差异性表达,cDNA进行克隆,针对已知基因序列进行对比分析同源性特点。结果 在本次研究结果中,克隆到18个与已知基因有高度同源性的cdna序列其中的基因组控制类型包括抗氧化损伤、线粒体跨膜运输细胞骨架以及系统相关基因。结论 三氧化二砷诱导的肝癌HCC-9204细胞出现凋亡后,大量的基因表达出现上调的特征,而这些基因与三氧化二砷处理肝癌系细胞后的应激反应与细胞凋亡有密切的关联性,针对本次研究结果进行判断,提示细胞凋亡具有多基因参与的特征,受到诸多基因类型的调控是一个极为复杂的过程。
关键词: 肝癌;细胞凋亡;基因类型;研究分析
Abstract
Objective To explore and analyze the apoptosis genes of liver cancer cells, analyze the corresponding gene sequence, and explore the molecular mechanism of arsenic trioxide on the apoptosis of liver cancer cells. Methods In this study, arsenic trioxide was used to induce apoptosis of human liver cancer HCC-9204 cells, and the differential expression in apoptotic cells was cloned by using inhibitory subtractive hybridization technology. Comparative analysis of homology characteristics. Results In this study, 18 cDNA sequences with high homology to known genes were cloned. The types of genome control include anti-oxidative damage, mitochondrial transmembrane transport cytoskeleton and system-related genes. Conclusion After arsenic trioxide-induced apoptosis of liver cancer HCC-9204 cells, a large number of gene expressions are up-regulated, and these genes are closely related to the stress response and apoptosis of liver cancer cells after arsenic trioxide treatment. Judging from the results of this study, it is suggested that apoptosis is characterized by the participation of multiple genes, and it is an extremely complex process that is regulated by many gene types.
Key words: liver cancer; apoptosis; gene type; research analysis
参考文献 References
[1] 鞠宝玲,海艳洁,鄂志野,张红军. miRNA–193a–3p靶向TGF–β2基因诱导肝癌细胞凋亡的分子机制研究[J]. 中国现代医生,2022,60(20):1-5.
[2] 陈科谚,何海洪,柯娟玉,余蕙君,张立俊,王静,周义文. Survivin基因在肝癌细胞增殖、凋亡过程中的表达及意义[J]. 海南医学,2021,32(04):409-412.
[3] 鲁斌,程敏,周凡. Bad联合Caspase-8促凋亡基因共表达对SK-HEP-1肝癌细胞体外增殖、凋亡、迁移和体内成瘤影响的实验研究[J]. 实用医学杂志,2020,36(08):1030-1034.
[4] 冯桂银,张庚,王海伦,梁东启,袁媛,樊艳. SOX7基因对肝癌细胞凋亡、氧化应激及Wnt/β-catenin信号通路的影响[J]. 蚌埠医学院学报,2019,44(07):846-849+854.
[5] 王浩南,李康,闫融,陈威,孙团鹤,王璇,朱琨,党诚学. 通过Crispr-cas9介导抑制KIAA0101基因可诱导肝癌细胞凋亡[J]. 山西医科大学学报,2019,50(06):709-714.
[6] 张俊,薛新波,申铭,郑建伟,肖朝文. 1mda-7/IL-24基因致肝癌细胞凋亡及增强其对ADM化疗敏感性的机制研究[J]. 世界最新医学信息文摘,2017,17(84):3-5+13.
[7] 李波,刘峰舟,刘明莉,李嘉琦,杨懿,宋子煜,张洪新,牟佼. NPAS2基因敲除的HepG2细胞系构建及其对肝癌细胞凋亡的影响[J]. 现代生物医学进展,2017,17(29):5618-5622.
[8] 肖朝文,王从俊,李明杰,蔡常春,郑建伟,申铭. 携带人黑色素瘤分化相关基因-7/白细胞介素-24基因的溶瘤腺病毒SG600-IL24选择性促进肝癌细胞凋亡和增殖阻滞[J]. 中华实验外科杂志,2017,34(07):1091-1094.