Phosphorylated ATF1 at Thr184 promotes metastasis and regulates MMP2 expression in gastric cancer

癌症研究 MMP2型 生物 转移 染色质免疫沉淀 磷酸化 分子生物学 癌症 基因表达 发起人 细胞生物学 生物化学 基因 遗传学
作者
Tong Li,Huiyuan Cao,Sa Wu,Peimin Zhong,Jie Ding,Jing Wang,Fangfang Wang,Zhiwei He,Guoliang Huang
出处
期刊:Journal of Translational Medicine [BioMed Central]
卷期号:20 (1) 被引量:9
标识
DOI:10.1186/s12967-022-03361-3
摘要

Studies have revealed an important role of activating transcription factor 1 (ATF1) and phosphorylated ATF1 at Ser63 in tumors. Our previous study identified Thr184 as a novel phosphorylation site of ATF1. However, the role of phosphorylated ATF1 at Thr184 (p-ATF1-T184) in tumor is unclear. This study figured out the role of p-ATF1-T184 in the metastasis of gastric cancer (GC) and in the regulation of Matrix metallopeptidase 2 (MMP2).Immunohistochemical analysis (IHC) was performed to analyze the level of p-ATF1-T184 and its relationship with clinicopathological characteristics. Wound scratch test, Transwell assay were used to observe the role of p-ATF1-T184 in the invasion and metastasis of GC. The regulation of MMP2 by p-ATF1-T184 was investigated by a series of experiments including quantitative RT-PCR, western blot, gelatin zymography assay, Chromatin immunoprecipitation (ChIP), luciferase reporter assay and cycloheximide experiment. The Cancer Genome Atlas (TCGA) data were used to analyze the expression and prognostic role of ATF1 and MMP2 in GC. Mass spectrometry (MS) following co-immunoprecipitation (co-IP) assay was performed to identify potential upstream kinases that would phosphorylate ATF1 at Thr184.High expression level of p-ATF1-T184 was found and significantly associated with lymph node metastasis and poor survival in a GC cohort of 126 patients. P-ATF1-T184 promoted migration and invasion of gastric cancer cells. Phosphorylation of ATF1-T184 could regulate the mRNA, protein expression and extracellular activity of MMP2. P-ATF1-T184 further increased the DNA binding ability, transcription activity, and stabilized the protein expression of ATF1. Moreover, TCGA data and IHC results suggested that the mRNA level of ATF1 and MMP2, and protein level of p-ATF1-T184 and MMP2 could be prognosis markers of GC. Two protein kinase related genes, LRBA and S100A8, were identified to be correlated with the expression ATF1 in GC.Our results indicated that p-ATF1-T184 promoted metastasis of GC by regulating MMP2.

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
body发布了新的文献求助10
1秒前
欣喜宛亦完成签到 ,获得积分10
1秒前
赵坤煊完成签到 ,获得积分10
1秒前
12243243完成签到,获得积分10
1秒前
科研通AI5应助是莉莉娅采纳,获得30
1秒前
hecarli完成签到,获得积分0
2秒前
2秒前
SciGPT应助顶呱呱采纳,获得10
3秒前
orixero应助科研小白采纳,获得10
3秒前
科研通AI5应助科研通管家采纳,获得10
4秒前
脑洞疼应助科研通管家采纳,获得10
4秒前
4秒前
Auston_zhong应助科研通管家采纳,获得20
4秒前
FashionBoy应助科研通管家采纳,获得10
4秒前
情怀应助科研通管家采纳,获得10
4秒前
领导范儿应助科研通管家采纳,获得10
4秒前
CodeCraft应助科研通管家采纳,获得10
4秒前
斯文败类应助科研通管家采纳,获得10
4秒前
英俊的铭应助科研通管家采纳,获得10
4秒前
阿飘应助科研通管家采纳,获得10
4秒前
顾矜应助科研通管家采纳,获得10
5秒前
5秒前
852应助科研通管家采纳,获得10
5秒前
SciGPT应助科研通管家采纳,获得20
5秒前
Hello应助科研通管家采纳,获得10
5秒前
ding应助科研通管家采纳,获得10
5秒前
英俊的铭应助科研通管家采纳,获得10
5秒前
wanci应助科研通管家采纳,获得10
5秒前
慕青应助科研通管家采纳,获得10
5秒前
5秒前
5秒前
wanci应助科研通管家采纳,获得10
5秒前
6秒前
爱学习的小李完成签到 ,获得积分10
7秒前
今后应助浪者漫心采纳,获得10
7秒前
SSY完成签到,获得积分10
7秒前
等待的音响完成签到,获得积分10
8秒前
8秒前
一二完成签到,获得积分10
9秒前
9秒前
高分求助中
【此为提示信息,请勿应助】请按要求发布求助,避免被关 20000
Production Logging: Theoretical and Interpretive Elements 3000
CRC Handbook of Chemistry and Physics 104th edition 1000
Density Functional Theory: A Practical Introduction, 2nd Edition 890
Izeltabart tapatansine - AdisInsight 600
Introduction to Comparative Public Administration Administrative Systems and Reforms in Europe, Third Edition 3rd edition 500
Distinct Aggregation Behaviors and Rheological Responses of Two Terminally Functionalized Polyisoprenes with Different Quadruple Hydrogen Bonding Motifs 450
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3761311
求助须知:如何正确求助?哪些是违规求助? 3305274
关于积分的说明 10133104
捐赠科研通 3019218
什么是DOI,文献DOI怎么找? 1658046
邀请新用户注册赠送积分活动 791820
科研通“疑难数据库(出版商)”最低求助积分说明 754655