LncRNATCF7 up-regulates DNMT1 mediated by HPV-18 E6 and regulates biological behavior of cervical cancer cells by inhibiting miR-155.

基因敲除 宫颈癌 DNMT1型 癌症研究 癌症 化学 癌细胞 报告基因 细胞培养 医学 生物 内科学 基因表达 基因 DNA甲基化 遗传学 生物化学
作者
Chen Yz,Wang Jw,Meng Fc,Po Yang,Zhang Xg,Wu Hz
出处
期刊:PubMed [National Institutes of Health]
卷期号:23 (20): 8779-8787 被引量:2
标识
DOI:10.26355/eurrev_201910_19272
摘要

This work aimed to study the mechanism of lncRNATCF7 upregulating DNMT1 mediated by HPV-18 E6 and regulating the biological behavior of cervical cancer cells by inhibiting miR-155.HPV-16 E6 enhanced DNMT1 expression in cervical cancer cells, which was detected by Western blotting. The expression of miR-155 in cervical cancer was detected by qPCR, the interaction between TCF-7 and miR-155 by Dual-luciferase reporter gene. The changes in invasion ability of cervical cancer cells and the effect of miR-155 on the invasion ability of cervical cancer cells after inhibiting TCF-7 were detected by the transwell invasion assay, while changes in migration ability of cervical cancer cells and the effect of miR-155 on migration ability of cervical cancer cells after inhibiting TCF-7 were observed by the scratch assay. The effect of inhibiting TCF-7 on the tumor size and volume of cervical cancer was detected by the subcutaneous tumor formation in nude mice.E6 expression was significantly inhibited by E6 siRNA. The knockdown of endogenous HPV-16 E6 markedly inhibited the expression of DNMT1; TCF-7 specifically bound to the 3' UTR of miR-155; inhibition of TCF-7 can inhibit invasion and migration of cervical cancer cells; enhanced miR-155 after the inhibition of TCF-7 can promote the invasion and migration of cervical cancer cells; compared with NC group, the tumor volume and weight of TCF-7-siRNA group tumor-bearing was significantly reduced.TCF-7 plays an important role in the development of cervical cancer. TCF-7 can target miR-155 to regulate the invasion and migration of cervical cancer cells.

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
科目三的应助被猪猪猪采纳,获得10
3秒前
3秒前
随意吧发布了新的文献求助20
3秒前
科研通AI6.2的应助被YYYYYYY采纳,获得10
3秒前
啊哈完成签到,获得积分10
3秒前
冻结完成签到 ,获得积分10
3秒前
4秒前
5秒前
wan完成签到 ,获得积分10
5秒前
万事顺遂完成签到,获得积分10
6秒前
情怀的应助被霍金会怎么做采纳,获得10
6秒前
6秒前
杨欢完成签到,获得积分10
6秒前
7秒前
8秒前
夜挽完成签到,获得积分10
8秒前
在水一方的应助被安详向梦采纳,获得30
8秒前
周全敏完成签到 ,获得积分10
8秒前
骆凤灵完成签到,获得积分10
9秒前
9秒前
wy.he举报LYH的求助涉嫌违规
9秒前
nan11发布了新的文献求助10
9秒前
9秒前
杨欢发布了新的文献求助10
10秒前
熊翠玲的应助被compell2022采纳,获得10
10秒前
10秒前
11秒前
molihuakai的应助被Allfine采纳,获得10
11秒前
陈门若市关注了科研通微信公众号
12秒前
lcz发布了新的文献求助10
12秒前
李健的应助被糕糕采纳,获得10
13秒前
13秒前
裴浩男完成签到,获得积分10
13秒前
13秒前
14秒前
立志做个化学人完成签到,获得积分10
14秒前
Steven发布了新的文献求助10
15秒前
满意完成签到,获得积分10
15秒前
英俊的铭的应助被dhz采纳,获得10
15秒前
哈哈完成签到,获得积分10
15秒前
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
Aspects of Post-SPE Phonology 2000
Performance standards for antimicrobial disk and dilution susceptibility tests for bacteria isolated from animals 888
Rosenblum, Global Change Biology 800
Holistic Discourse Analysis, Second Edition by Robert E. Longacre (2012-09-10) 666
Final Report for the 2-D Test of Model 901 Rotor and Wing Airfoils (BSWT 592) 528
Berberine regulates the TLR4 signaling pathway to suppress hypoxia-induced proliferation and migration of pulmonary arterial smooth muscle cells 520
热门求助领域 (近24小时)
化学 材料科学 医学 生物 计算机科学 工程类 纳米技术 物理 有机化学 化学工程 内科学 生物化学 复合材料 催化作用 心理学 细胞生物学 无机化学 电极 光电子学 人工智能
热门帖子
关注 科研通微信公众号,转发送积分 7889029
求助须知:如何正确求助?哪些是违规求助? 9400684
关于积分的说明 20841505
捐赠科研通 7491735
什么是DOI,文献DOI怎么找? 3357370
关于科研通互助平台的介绍 2495942
邀请新用户注册赠送积分活动 2385693