• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

衰老巨噬细胞与肺癌微环境:肿瘤免疫逃逸的新视角

Senescent Macrophages and the Lung Cancer Microenvironment: A New Perspective on Tumor Immune Evasion.

作者信息

Qin Lexin, Liang Tingting, Zhu Xinyu, Hu Wentao, Li Bo, Wei Meidan, Zhang Jiaxin, Li Jianxiang, Wang Jin

出版信息

Aging Dis. 2024 Dec 31. doi: 10.14336/AD.2024.1404.

DOI:10.14336/AD.2024.1404
PMID:39751858
Abstract

Lung cancer treatment is evolving, and the role of senescent macrophages in tumor immune evasion has become a key focus. This study explores how senescent macrophages interact with lung cancer cells, contributing to tumor progression and immune dysfunction. As aging impairs macrophage functions, including phagocytosis and metabolic signaling, it promotes chronic inflammation and cancer development. p16-positive macrophages are common in aged mice, and their clearance slows tumor growth, suggesting these cells support tumor proliferation and immune evasion. Targeting the senescence-associated secretory phenotype (SASP) and reprogramming senescent macrophages offers potential therapeutic benefits, including reversing immune aging and boosting anti-tumor immunity. However, translating these findings into clinical practice requires further molecular understanding and rigorous clinical trials.

摘要

肺癌治疗正在不断发展,衰老巨噬细胞在肿瘤免疫逃逸中的作用已成为关键焦点。本研究探讨衰老巨噬细胞如何与肺癌细胞相互作用,促进肿瘤进展和免疫功能障碍。随着衰老损害巨噬细胞功能,包括吞噬作用和代谢信号传导,它会促进慢性炎症和癌症发展。p16阳性巨噬细胞在老年小鼠中很常见,清除它们可减缓肿瘤生长,表明这些细胞支持肿瘤增殖和免疫逃逸。靶向衰老相关分泌表型(SASP)并对衰老巨噬细胞进行重编程具有潜在的治疗益处,包括逆转免疫衰老和增强抗肿瘤免疫力。然而,将这些发现转化为临床实践需要进一步的分子理解和严格的临床试验。

相似文献

1
Senescent Macrophages and the Lung Cancer Microenvironment: A New Perspective on Tumor Immune Evasion.衰老巨噬细胞与肺癌微环境:肿瘤免疫逃逸的新视角
Aging Dis. 2024 Dec 31. doi: 10.14336/AD.2024.1404.
2
Combined targeting of senescent cells and senescent macrophages: A new idea for integrated treatment of lung cancer.衰老细胞与衰老巨噬细胞的联合靶向治疗:肺癌综合治疗的新思路。
Semin Cancer Biol. 2024 Nov;106-107:43-57. doi: 10.1016/j.semcancer.2024.08.006. Epub 2024 Aug 29.
3
A new model and precious tool to study molecular mechanisms of macrophage aging.一种研究巨噬细胞衰老分子机制的新模型和宝贵工具。
Aging (Albany NY). 2024 Oct 3;16(19):12697-12725. doi: 10.18632/aging.206124.
4
Aging of mice is associated with p16(Ink4a)- and β-galactosidase-positive macrophage accumulation that can be induced in young mice by senescent cells.小鼠衰老与p16(Ink4a)和β-半乳糖苷酶阳性巨噬细胞的积累有关,衰老细胞可在年轻小鼠中诱导这种积累。
Aging (Albany NY). 2016 Jul;8(7):1294-315. doi: 10.18632/aging.100991.
5
Tumor cell senescence-induced macrophage CD73 expression is a critical metabolic immune checkpoint in the aging tumor microenvironment.肿瘤细胞衰老诱导的巨噬细胞 CD73 表达是衰老肿瘤微环境中关键的代谢免疫检查点。
Theranostics. 2024 Jan 20;14(3):1224-1240. doi: 10.7150/thno.91119. eCollection 2024.
6
Cellular Senescence in Diabetes Mellitus: Distinct Senotherapeutic Strategies for Adipose Tissue and Pancreatic β Cells.糖尿病中的细胞衰老:脂肪组织和胰腺 β 细胞的独特衰老治疗策略。
Front Endocrinol (Lausanne). 2022 Mar 31;13:869414. doi: 10.3389/fendo.2022.869414. eCollection 2022.
7
Clearance of senescent macrophages ameliorates tumorigenesis in KRAS-driven lung cancer.清除衰老的巨噬细胞可改善 KRAS 驱动的肺癌的肿瘤发生。
Cancer Cell. 2023 Jul 10;41(7):1242-1260.e6. doi: 10.1016/j.ccell.2023.05.004. Epub 2023 Jun 1.
8
Similarities and interplay between senescent cells and macrophages.衰老细胞与巨噬细胞之间的相似性和相互作用。
J Cell Biol. 2021 Feb 1;220(2). doi: 10.1083/jcb.202010162.
9
SASP-induced macrophage dysfunction may contribute to accelerated senescent fibroblast accumulation in the dermis.柳氮磺胺吡啶诱导的巨噬细胞功能障碍可能导致真皮中衰老成纤维细胞加速积累。
Exp Dermatol. 2021 Jan;30(1):84-91. doi: 10.1111/exd.14205. Epub 2020 Dec 20.
10
Tumor suppressor and aging biomarker p16(INK4a) induces cellular senescence without the associated inflammatory secretory phenotype.肿瘤抑制因子和衰老生物标志物 p16(INK4a) 在没有相关炎症分泌表型的情况下诱导细胞衰老。
J Biol Chem. 2011 Oct 21;286(42):36396-403. doi: 10.1074/jbc.M111.257071. Epub 2011 Aug 31.

引用本文的文献

1
GART promotes the proliferation and migration of human non-small cell lung cancer cell lines A549 and H1299 by targeting PAICS-Akt-β-catenin pathway.GART通过靶向PAICS-Akt-β-连环蛋白通路促进人非小细胞肺癌细胞系A549和H1299的增殖和迁移。
Front Oncol. 2025 Mar 25;15:1543463. doi: 10.3389/fonc.2025.1543463. eCollection 2025.
2
Exploring the classification and treatment of osteoporosis from the perspectives of natural medicines, molecular targets, and symptom clusters.从天然药物、分子靶点和症状群的角度探索骨质疏松症的分类与治疗。
Sci Rep. 2025 Mar 25;15(1):10218. doi: 10.1038/s41598-025-95304-3.