ZNF746 promotes M2 macrophage polarisation and favours tumour progression in breast cancer via the Jagged1/Notch pathway

川地163 赫斯1 癌症研究 Notch信号通路 免疫组织化学 基因敲除 细胞生长 生物 细胞迁移 癌变 巨噬细胞 细胞 癌症 信号转导 细胞生物学 细胞培养 免疫学 体外 遗传学 生物化学
作者
Lu Liu,Wenyue Zhao,Xinyu Zheng
出处
期刊:Cellular Signalling [Elsevier]
卷期号:112: 110892-110892 被引量:6
标识
DOI:10.1016/j.cellsig.2023.110892
摘要

Breast cancer (BC) is a major threat to women's health. BC is a heterogeneous disease and treatment strategies and outcomes differ between subtypes. Investigating the molecular mechanisms of BC will help to identify potential therapeutic targets and develop new therapies. Here we report that zinc finger protein 746 (ZNF746), a Krüppel-associated box and zinc finger protein, exhibits tumour-promoting properties in BC. Functional experiments (cell growth, colony formation, cell cycle analysis, and transwell analysis) were used to evaluate the proliferation, migration, and invasion capacity of BC cells. Immunohistochemistry was performed to detect the expression of ZNF746, CD163 (M2 macrophage marker), and HES1 (Notch target) in BC tissues. ZNF746 was highly expressed in BC tissues compared to adjacent paired non-tumour tissues. Patients with M1 BC had higher expression of ZNF746 compared to patients with non-metastatic (M0) BC, and higher expression of ZNF746 was associated with poorer overall survival. The immunohistochemical results showed a positive correlation between the expression of ZNF746 and the expression of CD163 or HES1. ZNF746 promoted BC cell proliferation, migration, and invasion and increased the expression of molecules essential for monocyte recruitment and differentiation (CCL2 and CSF1). Furthermore, THP-1 monocytes cultured in the conditioned medium derived from BC cells overexpressing ZNF746 exhibited enhanced M2 polarisation. In contrast, ZNF746 knockdown reduced BC cell proliferation, migration, and invasion and suppressed M2 polarisation. Mechanistically, ZNF746 promoted the activation of the Jagged1/Notch pathway, and the Jagged1 siRNA-mediated blockade of this pathway prevented the tumour-promoting functions of ZNF746. In conclusion, this study uncovers the role of ZNF746 in promoting M2 macrophage polarisation and suggests that ZNF746 may be a promising therapeutic target for limiting BC progression.
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
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
阿发发布了新的文献求助10
刚刚
1秒前
1秒前
2秒前
huihui发布了新的文献求助50
4秒前
ZHZ关闭了ZHZ文献求助
4秒前
上官若男应助努力的咩咩采纳,获得10
4秒前
6秒前
mty完成签到,获得积分10
6秒前
乐乐应助研友_nV21Vn采纳,获得10
6秒前
7秒前
7秒前
共享精神应助css采纳,获得10
7秒前
王占雪完成签到 ,获得积分10
7秒前
林志坚完成签到 ,获得积分10
7秒前
ZEABIA发布了新的文献求助10
7秒前
wz1666发布了新的文献求助10
7秒前
大力的灵雁应助罗坛坛采纳,获得20
8秒前
LUJL发布了新的文献求助10
8秒前
传奇3应助一颗杨桃采纳,获得10
8秒前
9秒前
lucky发布了新的文献求助10
10秒前
香蕉觅云应助冰淇淋真凉采纳,获得10
10秒前
小囧发布了新的文献求助10
10秒前
网络乞丐完成签到,获得积分10
11秒前
mty发布了新的文献求助10
11秒前
万能图书馆应助zzy采纳,获得10
11秒前
科滴滴发布了新的文献求助10
12秒前
12秒前
depravity发布了新的文献求助10
12秒前
renrunxue发布了新的文献求助10
12秒前
13秒前
年轻烤鸡发布了新的文献求助10
13秒前
h3rry发布了新的文献求助10
13秒前
13秒前
JamesPei应助zzz采纳,获得10
13秒前
哈哈哈哈发布了新的文献求助10
14秒前
择城发布了新的文献求助10
14秒前
小羊佳佳发布了新的文献求助10
14秒前
14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
Handbook of pharmaceutical excipients, Ninth edition 5000
Aerospace Standards Index - 2026 ASIN2026 3000
Digital Twins of Advanced Materials Processing 2000
Polymorphism and polytypism in crystals 1000
Signals, Systems, and Signal Processing 610
Discrete-Time Signals and Systems 610
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 纳米技术 有机化学 物理 生物化学 化学工程 计算机科学 复合材料 内科学 催化作用 光电子学 物理化学 电极 冶金 遗传学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 6040648
求助须知:如何正确求助?哪些是违规求助? 7777390
关于积分的说明 16231667
捐赠科研通 5186723
什么是DOI,文献DOI怎么找? 2775557
邀请新用户注册赠送积分活动 1758586
关于科研通互助平台的介绍 1642207