期刊文献+

纳米材料调控肿瘤相关巨噬细胞进行肿瘤免疫治疗的研究进展

Progress of Nanomaterials Regulating Tumor-Associated Macrophages for Tumor Immunotherapy
下载PDF
导出
摘要 骨髓源巨噬细胞和组织常驻巨噬细胞,统称为肿瘤相关巨噬细胞(Tumor-Associated Macrophages, TAMs),存在于肿瘤微环境中,在肿瘤治疗方面备受关注。本文在阐明TAMs促肿瘤生长机制的基础上,总结了靶向TAMs的作用机制和治疗策略,重点介绍了纳米药物载体如何通过靶向调控TAMs进行肿瘤的免疫治疗。纳米药物载体主要通过阻断TAMs的存活或影响其信号级联、限制TAMs向肿瘤的募集以及逆转促肿瘤的M2型TAMs至抗肿瘤的M1型发挥抗肿瘤作用。以上内容显示纳米材料由于其特殊的物化性质,能够靶向TAMs,并通过多种途径调控TAMs,增强抗肿瘤免疫反应,具有非常好的免疫治疗的发展前景。 Macrophages derived from bone marrow and tissue resident macrophages, collectively referred to as tumor associated macrophages (TAMs), are present in the tumor microenvironment and have attracted considerable attention in the treatment of tumors. Based on the clarification of the mechanism of TAMs to promote tumor growth, this article summarizes the mechanism of action and treatment strategies of targeted TAMs and focuses on how nanomedicine carriers can target tumor immunotherapy through targeted TAMs regulation. Nanodrug carriers have an antitumor effect mainly by preventing the survival of TAMs or disrupting their signal cascades, reducing the recruitment of TAMs to tumors, and reversing the tumor promoting M2 type TAMs to the antitumor type M1. The above content shows that, due to their different physical and chemical properties, nanomaterials can target TAMs and regulate TAMs in a number of ways to enhance the antitumor immune response, which has very good prospects for growth in immunotherapy.
作者 徐睿 刘晨光
机构地区 中国海洋大学
出处 《材料科学》 CAS 2020年第2期75-83,共9页 Material Sciences
基金 受山东省重点研发项目(2019GSF107031)资助。
  • 相关文献

参考文献1

二级参考文献20

  • 1Oh SC.Update of adjuvant chemotherapy for resected gastric can-cer[J].J Gastric Cancer,2012,12(1):3-6.
  • 2Ishigami S,Natsugoe S,Tokuda K,et al.Tumor-associated macro-phage(TAM)infiltration in gastric cancer[J].Anticancer Res,2003,23(5A):4079-4083.
  • 3Ohno S,Inagawa H,Dhar DK,et al.The degree of macrophage in-filtration into the cancer cell nest is a significant predictor of survivalin gastric cancer patients[J].Anticancer Res,2003,23(6D):5015-5022.
  • 4Solinas G,Germano G,Mantovani A,et al.Tumor-associated mac-rophages(TAM)as major players of the cancer-related inflamma-tion[J].J Leukoc Biol,2009,86(5):1065-1073.
  • 5Biswas SK,Sica A,Lewis CE.Plasticity of macrophage functionduring tumor progression:regulation by distinct molecular mecha-nisms [J].J Immunol,2008,180(4):2011-2017.
  • 6Senovilla L,Vacchelli E,GaIon J,et al.Trial watch:Prognostic andpredictive value of the immune infiltrate in cancer[J].Oncoimmunol-ogy,2012,1(8):1323-1343.
  • 7Ohta M,Kitadai Y,Tanaka S,et al.Monocyte chemoattractant pro-tein-I expression correlates with macrophage infiltration and tu-mor vascularity in human gastric carcinomas[J].IntJ Oncol,2003,22(4):773-778.
  • 8Oshima H,Hioki K,Popivanova BK,et al.Prostaglandin E2 signal-ing and bacterial infection recruit tumor-promoting macrophagesto mouse gastric tumors[J].Gastroenterology,2011,140(2):596-607.
  • 9Quiding-Jarbrink M,Raghavan S,Sundquist M.Enhanced Mlmacrophage polarization in human helicobacter pylori-associatedatrophic gastritis and in vaccinated mice[J].PLoS One,2010,5(11):el5018.
  • 10Lu P,Weaver VM,Werb Z.The extracellular matrix:a dynamicniche in cancer progression[J].J Cell Biol,2012,196(4):395-406.

共引文献5

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部