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作 者:杨梦莉[1] 陈香岭 隋旭[2] 廉亚茹 马春霞[1] 姚宇峰[1] 史荔[1] 马千里[3] 俞建昆[1] YANG Mengli CHEN Xiangling SUI Xu LIAN Yaru MA Chunxia YAO Yufeng SHI Li MA Qianli YU Jiankun(Institute of Medical Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, Kunming 650118, Yunnan , China Kunming University of Science and Technology, Kunming 650093, Yunann , China Department of Thoracic Surgery, the Third Affiliated Hospital of Kunming Medical University, Kunming 650118, Yunnan, China)
机构地区:[1]中国医学科学院,北京协和医学院,医学生物学研究所,云南昆明650118 [2]昆明理工大学,云南昆明650093 [3]昆明医科大学第三附属医院胸外科,云南昆明650118
出 处:《贵州医科大学学报》2016年第11期1279-1284,共6页Journal of Guizhou Medical University
基 金:中国医学科学院病原生物学研究所基本科研业务费项目(2012IPB107);高等学校博士学科点专项科研基金(新教师类)(20111106120056)
摘 要:目的:利用顺铂处理肺癌、宫颈癌细胞和人胚肾细胞,检测人类端粒酶逆转录酶催化亚单位(hTERT)mRNA的选择性剪接是否发生变化。方法:将培养的肺癌A549和H1299细胞,宫颈癌C33A、SiHa和Ca Ski细胞及人胚肾293FT细胞分为实验组和对照组,用顺铂处理实验组细胞,DMSO处理对照组细胞;设计hTERTα+β+、α+β-、α-β+、INS3及DEL[e2]引物,提取两组细胞的总RNA,利用RT-PCR检测hTERT mRNA剪接异构体表达。结果:与对照组细胞相比,随着顺铂浓度的增加,肺癌A549和H1299细胞,宫颈癌C33A、SiHa和Ca Ski细胞以及人胚肾293FT细胞中hTERTα+β-和INS3异构体比例升高,而DEL[e2]异构体变化不明显。结论:在顺铂引起的DNA损伤情况下,细胞可利用hTERT mRNA选择性剪接调控机制进行调节,通过改变不同异构体的量和所占比例,从而调节端粒酶功能活性。Objective:To determine whether there is any change of alternative splicing of hTERT mRNA in lung cancer and cervical cancer cells and human embryonic kidney cells after cisplatin treat-ment,different dose of cisplatin were used to treat these two types of cell line. Methods:Cultivated lung cancer A549 and H1299 cells,cervical cancer C33A,SiH aand CaSki cells and HEK 293FT cells were divided into experiment group and control group;using cisplatin to treat experiment group cells and DMSO to treat control group cells;hTERTα+β+,α+β-,α-β+,INS3 ,DEL[ e2 ]alter-native splicing sites were selected to design primers. Total RNA of treated cells and control cells after treatment with cisplatin were extracted and RT-PCR was used to test the spliced transcripts,and their ratios of hTERT mRNA in cancer cells. Results:The results indicated that the ratio of the hTERTα+β- and INS3 isoform increased with the increase of the concentration of cisplatin;but the change of DEL[e2]was not obvious. Conclusion:The activity of telomerase may be regulated through the ex-pression and ratio of different alternative splicing isoforms of hTERT when DNA impairment.
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