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 生物化学 遗传学
作者
Lixin Lu,Wenyue Zhao,Xinyu Zheng
出处
期刊:Cellular Signalling [Elsevier]
卷期号:112: 110892-110892
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
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
1秒前
雪山发布了新的文献求助10
1秒前
2秒前
蓝桉哦完成签到,获得积分10
2秒前
CodeCraft应助张张采纳,获得10
5秒前
狂野白梅发布了新的文献求助10
6秒前
会飞的云完成签到 ,获得积分10
6秒前
传奇3应助的如采纳,获得10
7秒前
十七完成签到,获得积分10
7秒前
Owen应助112采纳,获得10
7秒前
9秒前
科研通AI2S应助科研通管家采纳,获得10
9秒前
9秒前
orixero应助科研通管家采纳,获得10
9秒前
天天快乐应助科研通管家采纳,获得10
9秒前
9秒前
10秒前
深渊发布了新的文献求助10
10秒前
坚定的鼠标应助能干夏波采纳,获得10
10秒前
13秒前
852应助无奈鸣凤采纳,获得10
13秒前
14秒前
星辰大海应助拉萨小医生采纳,获得10
14秒前
斯文败类应助狂野白梅采纳,获得10
18秒前
无尤发布了新的文献求助10
18秒前
19秒前
qqqqq发布了新的文献求助10
21秒前
22秒前
23秒前
23秒前
24秒前
知趣完成签到 ,获得积分10
25秒前
yuan发布了新的文献求助10
26秒前
嘉月yue完成签到,获得积分10
28秒前
qqqqq完成签到,获得积分10
29秒前
29秒前
俏皮不可发布了新的文献求助30
30秒前
31秒前
31秒前
32秒前
高分求助中
Teaching Social and Emotional Learning in Physical Education 900
Plesiosaur extinction cycles; events that mark the beginning, middle and end of the Cretaceous 800
Recherches Ethnographiques sue les Yao dans la Chine du Sud 500
Two-sample Mendelian randomization analysis reveals causal relationships between blood lipids and venous thromboembolism 500
Chinese-English Translation Lexicon Version 3.0 500
[Lambert-Eaton syndrome without calcium channel autoantibodies] 440
Wisdom, Gods and Literature Studies in Assyriology in Honour of W. G. Lambert 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 有机化学 工程类 生物化学 纳米技术 物理 内科学 计算机科学 化学工程 复合材料 遗传学 基因 物理化学 催化作用 电极 光电子学 量子力学
热门帖子
关注 科研通微信公众号,转发送积分 2389985
求助须知:如何正确求助?哪些是违规求助? 2096030
关于积分的说明 5279822
捐赠科研通 1823162
什么是DOI,文献DOI怎么找? 909483
版权声明 559621
科研通“疑难数据库(出版商)”最低求助积分说明 485999