Research on Mechanism of miR-214 Packaged with Lipidosome Nanoparticles on Prompting the Apoptosis of Intestinal Cancer Through Regulating p53 Pathway

敌手 细胞凋亡 兴奋剂 癌细胞 化学 细胞生物学 药理学 癌症研究 癌症 内科学 生物 医学 受体 生物化学
作者
Fan Yang,Runjia Fan,Miaomiao Gou,Qinna Yang,Tian‐Lan Zhang,Guanghai Dai,Niansong Qian
出处
期刊:Journal of Biomedical Nanotechnology [American Scientific Publishers]
卷期号:17 (12): 2391-2398 被引量:5
标识
DOI:10.1166/jbn.2021.3212
摘要

Our study aimed at studying mechanism of miR-214 packaged with lipidosome nanoparticles on prompting apoptosis of intestinal cancer through regulating p53 pathway. SW480 cells were divided into blank group, empty carrier group, agonist group and group with carrier and antagonist. The negative control group was set, and groups related to p53 pathway were set as agonist group, inhibitor group and group with antagonist and inhibitor. The effect of miR-214 packaged with lipidosome nanoparticles on proliferation and apoptosis of intestinal cancer cells and p53 pathway in intestinal cancer cells was observed. Expression level of miR-214 in group with carrier and antagonist was lower than in other groups. The proportion of active cells in the group with carrier and antagonist started to be reduced notably from the second day. There was no notable declining tendency active cells' proportion from other groups. The quantity of cell apoptosis in group with carrier and antagonist was higher than in the other groups. The expression level of cleaved Caspase-3 in the group with carrier and antagonist was notably higher than in the other groups. Moreover, expression of Bcl-2/Bax protein was reversed, while expression of p53 protein in the carrier and antagonist groups was notably higher than in the other groups. The antagonist of miR-214 packaged with lipidosome nanoparticles could target on p53 pathway. The activity of p53 pathway was reduced by miR-214, and expression of Bcl-2 was increased. The expressions levels of Bax and cleaved Caspase-3 were also reversed, and molecular mechanism was mainly related with restraining of p53 signal pathway.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
大幅提高文件上传限制,最高150M (2024-4-1)

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
刻苦从阳完成签到,获得积分10
5秒前
8秒前
阿木木发布了新的文献求助10
13秒前
langzhiquan完成签到,获得积分10
17秒前
七月星河完成签到 ,获得积分10
19秒前
从容芮应助科研通管家采纳,获得10
22秒前
从容芮应助科研通管家采纳,获得10
22秒前
danli完成签到 ,获得积分10
27秒前
李健春完成签到 ,获得积分10
27秒前
策策策策策完成签到 ,获得积分0
28秒前
WoeL.Aug.11完成签到 ,获得积分10
31秒前
yu_z完成签到 ,获得积分10
39秒前
111完成签到 ,获得积分10
41秒前
阿木木完成签到,获得积分10
43秒前
马大翔完成签到,获得积分10
46秒前
celia完成签到 ,获得积分10
51秒前
53秒前
一叶飘红完成签到,获得积分10
57秒前
alys发布了新的文献求助10
59秒前
nicheng完成签到 ,获得积分0
1分钟前
小潘完成签到 ,获得积分10
1分钟前
NOTHING完成签到 ,获得积分10
1分钟前
alys完成签到,获得积分10
1分钟前
1分钟前
柠檬完成签到 ,获得积分10
1分钟前
Laow发布了新的文献求助10
1分钟前
粥粥完成签到,获得积分10
1分钟前
英俊的铭应助Laow采纳,获得10
1分钟前
车水完成签到 ,获得积分10
1分钟前
ekko完成签到 ,获得积分10
1分钟前
1分钟前
lmz完成签到,获得积分10
1分钟前
sheila完成签到 ,获得积分10
1分钟前
安静严青完成签到 ,获得积分10
1分钟前
今后应助木光采纳,获得10
1分钟前
FF完成签到,获得积分10
2分钟前
Yuchengliu完成签到 ,获得积分10
2分钟前
平常雨泽完成签到 ,获得积分10
2分钟前
领导范儿应助Wang采纳,获得10
2分钟前
谜语完成签到 ,获得积分10
2分钟前
高分求助中
Evolution 2024
Impact of Mitophagy-Related Genes on the Diagnosis and Development of Esophageal Squamous Cell Carcinoma via Single-Cell RNA-seq Analysis and Machine Learning Algorithms 2000
Experimental investigation of the mechanics of explosive welding by means of a liquid analogue 1060
Die Elektra-Partitur von Richard Strauss : ein Lehrbuch für die Technik der dramatischen Komposition 1000
How to Create Beauty: De Lairesse on the Theory and Practice of Making Art 1000
Gerard de Lairesse : an artist between stage and studio 670
大平正芳: 「戦後保守」とは何か 550
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 催化作用 物理化学 免疫学 量子力学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 3004819
求助须知:如何正确求助?哪些是违规求助? 2664111
关于积分的说明 7220039
捐赠科研通 2300641
什么是DOI,文献DOI怎么找? 1220172
科研通“疑难数据库(出版商)”最低求助积分说明 594585
版权声明 593226