亲爱的研友该休息了!由于当前在线用户较少,发布求助请尽量完整地填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!身体可是革命的本钱,早点休息,好梦!

[Expression changes of tumor metastasis-related genes after overexpression of KAI1 in retinoblastoma Y79 cells].

视网膜母细胞瘤 转染 分子生物学 转移抑制基因 嘌呤霉素 绿色荧光蛋白 信使核糖核酸 基因 生物 细胞培养 基因表达 癌症研究 蛋白质生物合成 遗传学
作者
Xunda Ji,Hui Yan,Peiquan Zhao
出处
期刊:PubMed [National Institutes of Health]
卷期号:48 (12): 1097-101 被引量:1
链接
标识
摘要

To investigate the expression changes of tumor metastasis-related genes after overexpression of KAI1 in retinoblastoma Y79 cells.Experimental study. Y79 cells were transfected with a lentivirus vector containing KAI1 and enhanced green fluorescent protein (EGFP) fusion gene, or a control lentivirus vector containing EGFP. Positive transfectants stably expressing high levels of KAI1 were named Y79-KAI1 and control transfectants were named Y79-KAI1/zero. These transfectants were selected by puromycin resistance and analysis with fluorescent microscopy. The expression of KAI1 mRNA and its protein among Y79, Y79-KAI1 and Y79-KAI1/zero were detected by fluorescent quantitative RT-PCR and Western blot. Differential expression of tumor metastasis-related genes in Y79-KAI1 and Y79-KAI1/zero was analyzed with human tumor metastasis PCR array. One-way ANOVA was used to analyze the differences of KAI1 mRNA and protein expression among the three groups.The stably transfected cell lines of Y79-KAI1 and Y79-KAI1/zero were established. The result of fluorescent quantitative real-time PCR showed that the relative quantification of mRNA level of KAI1 gene in the three kinds of cells above was 183.67 ± 21.20, 1.42 ± 0.55, 1.00 ± 0.00, respectively. And the expression level of KAI1 mRNA in Y79-KAI1 cells was significantly higher than those in Y79-KAI1/zero and Y79 cells (F = 108.74, P = 0.000). The results of Western blot showed that the expression level of the KAI1 protein in Y79-KAI1 cells was significantly higher than those in Y79-KAI1/zero and Y79 cells (F = 34.36, P = 0.001). Immunofluorescent staining showed that Y79 and Y79-KAI1/zero cells had no detectable KAI1 expression, while Y79-KAI1 cells expressed KAI1 in the cytoplasm surrounding the nuclei. Among the 84 tumor metastasis-related genes examined, 7 genes were up-regulated more than 2 folds and 6 genes were down-regulated over 50%.Over-expression of KAI1 may result in differential expression of tumor metastasis-related genes in Y79 cells, which may be related to the inhibitory effect on the tumor metastasis of retinoblastoma.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
luckyaaahealthy完成签到,获得积分10
3秒前
13秒前
Liberty发布了新的文献求助10
18秒前
20秒前
WANG发布了新的文献求助10
26秒前
幸福海之完成签到,获得积分10
28秒前
WANG完成签到,获得积分10
36秒前
Liberty完成签到,获得积分10
41秒前
CipherSage应助WYZ采纳,获得10
42秒前
修辛完成签到 ,获得积分10
45秒前
zzz完成签到 ,获得积分10
47秒前
龙猫抱枕完成签到,获得积分10
50秒前
54秒前
hhuajw完成签到,获得积分10
57秒前
WYZ发布了新的文献求助10
58秒前
59秒前
shenjuan1674发布了新的文献求助10
1分钟前
心灵美若蓝完成签到 ,获得积分10
1分钟前
寒冷的映冬完成签到,获得积分10
1分钟前
Zhou完成签到,获得积分10
1分钟前
zhu完成签到,获得积分10
1分钟前
小马甲应助shenjuan1674采纳,获得10
1分钟前
Ru完成签到 ,获得积分10
1分钟前
1分钟前
生动的向日葵完成签到,获得积分10
1分钟前
cc应助科研通管家采纳,获得10
1分钟前
1分钟前
cc应助科研通管家采纳,获得10
1分钟前
cdercder应助科研通管家采纳,获得10
1分钟前
单纯水桃完成签到,获得积分10
2分钟前
2分钟前
小吉利完成签到,获得积分10
2分钟前
2分钟前
小吉利发布了新的文献求助10
2分钟前
shenjuan1674发布了新的文献求助10
2分钟前
学不完了发布了新的文献求助10
2分钟前
chen发布了新的文献求助10
3分钟前
shenjuan1674完成签到,获得积分10
3分钟前
悲凉的雁芙完成签到,获得积分10
3分钟前
青梅煮酒完成签到,获得积分10
3分钟前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
Practical Process Research and Development 500
Discerning Saints: Moralization of Intrinsic Motivation and Selective Prosociality at Work 500
Handbuch Trainingswissenschaft – Trainingslehre 500
Additive Manufacturing Design and Applications (ASM Handbook, Volume 24A) 500
Exploring Entrepreneurial Psychology Through AI 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7585568
求助须知:如何正确求助?哪些是违规求助? 9163893
关于积分的说明 19611696
捐赠科研通 7166722
什么是DOI,文献DOI怎么找? 3266600
关于科研通互助平台的介绍 2431601
邀请新用户注册赠送积分活动 2258310