Tumor-educated Neutrophils Induce Epithelial-mesenchymal Transition and Metastasis in Colorectal Cancer Through Interleukin-17a Secretion

IF 3.7 3区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Cytokine Pub Date : 2025-06-01 Epub Date: 2025-03-28 DOI:10.1016/j.cyto.2025.156928
Yibing Gong , Qingshuang Luo , Haiqi Tan , Jingyi Long , Longtai Hu , Moyed abd alhussain Hamza Al-saadawe , Jinke Yao , Xiaoming Lyu , Lizhen Qiu , Gongfa Wu
{"title":"Tumor-educated Neutrophils Induce Epithelial-mesenchymal Transition and Metastasis in Colorectal Cancer Through Interleukin-17a Secretion","authors":"Yibing Gong ,&nbsp;Qingshuang Luo ,&nbsp;Haiqi Tan ,&nbsp;Jingyi Long ,&nbsp;Longtai Hu ,&nbsp;Moyed abd alhussain Hamza Al-saadawe ,&nbsp;Jinke Yao ,&nbsp;Xiaoming Lyu ,&nbsp;Lizhen Qiu ,&nbsp;Gongfa Wu","doi":"10.1016/j.cyto.2025.156928","DOIUrl":null,"url":null,"abstract":"<div><div>The role of neutrophils in defending against infections and regulating immune responses is well-known. In cancer, tumor-associated neutrophils also play a significant role in the progression of tumors. However, the specific mechanisms of their interaction with human colorectal tumors have not been fully elucidated. Our study found that tumor-educated neutrophils can activate the STAT3 signaling pathway in colorectal cancer cells by secreting IL-17a. This leads to increased migration and invasion of colorectal cancer cells, promoting tumor growth by triggering epithelial-to-mesenchymal transition (EMT). These findings suggest that IL-17a secreted by tumor-educated neutrophils contributes to the development of colorectal cancer through the IL-17a/STAT3 signaling pathway. This provides new insights for potential treatments for colorectal cancer.</div></div>","PeriodicalId":297,"journal":{"name":"Cytokine","volume":"190 ","pages":"Article 156928"},"PeriodicalIF":3.7000,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cytokine","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1043466625000754","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/3/28 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

The role of neutrophils in defending against infections and regulating immune responses is well-known. In cancer, tumor-associated neutrophils also play a significant role in the progression of tumors. However, the specific mechanisms of their interaction with human colorectal tumors have not been fully elucidated. Our study found that tumor-educated neutrophils can activate the STAT3 signaling pathway in colorectal cancer cells by secreting IL-17a. This leads to increased migration and invasion of colorectal cancer cells, promoting tumor growth by triggering epithelial-to-mesenchymal transition (EMT). These findings suggest that IL-17a secreted by tumor-educated neutrophils contributes to the development of colorectal cancer through the IL-17a/STAT3 signaling pathway. This provides new insights for potential treatments for colorectal cancer.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
肿瘤诱导的中性粒细胞通过白细胞介素-17a分泌诱导结直肠癌上皮-间质转化和转移
中性粒细胞在防御感染和调节免疫反应中的作用是众所周知的。在癌症中,肿瘤相关的中性粒细胞在肿瘤的进展中也起着重要的作用。然而,它们与人类结直肠肿瘤相互作用的具体机制尚未完全阐明。我们的研究发现,肿瘤诱导的中性粒细胞可以通过分泌IL-17a激活结直肠癌细胞中的STAT3信号通路。这导致结直肠癌细胞的迁移和侵袭增加,通过触发上皮-间质转化(EMT)促进肿瘤生长。这些发现表明,由肿瘤诱导的中性粒细胞分泌的IL-17a通过IL-17a/STAT3信号通路参与结直肠癌的发展。这为结直肠癌的潜在治疗提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Cytokine
Cytokine 医学-免疫学
CiteScore
7.60
自引率
2.60%
发文量
262
审稿时长
48 days
期刊介绍: The journal Cytokine has an open access mirror journal Cytokine: X, sharing the same aims and scope, editorial team, submission system and rigorous peer review. * Devoted exclusively to the study of the molecular biology, genetics, biochemistry, immunology, genome-wide association studies, pathobiology, diagnostic and clinical applications of all known interleukins, hematopoietic factors, growth factors, cytotoxins, interferons, new cytokines, and chemokines, Cytokine provides comprehensive coverage of cytokines and their mechanisms of actions, 12 times a year by publishing original high quality refereed scientific papers from prominent investigators in both the academic and industrial sectors. We will publish 3 major types of manuscripts: 1) Original manuscripts describing research results. 2) Basic and clinical reviews describing cytokine actions and regulation. 3) Short commentaries/perspectives on recently published aspects of cytokines, pathogenesis and clinical results.
期刊最新文献
Association between neutrophil percentage-to-albumin ratio and sleep disorders risk: insights from a large US population-based study Experimental and data modeling approaches of umbilical cord blood allogenic response identify cytokine profiles as potential biomarkers associated with the initial stages of alloreactivity and immunomodulation Changes in the gut intra-epithelial lymphocyte landscape induced by erythropoietin treatment in a non-diseased mouse model Cytokine polarized natural killer T cells modulate effector T cell function in leprosy Combination therapy with amphotericin B and Ultradiluted Leishmania donovani antigen skews cytokine balance towards protective immunity in visceral leishmaniasis
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1