Tumor Associated Macrophages and TAMs-Based Anti-Tumor Nanomedicines

被引:64
作者
Cheng, Yuxi [1 ]
Song, Siyang [1 ]
Wu, Peiyao [1 ]
Lyu, Bochen [1 ]
Qin, Mengmeng [1 ]
Sun, Yanan [1 ]
Sun, Aning [1 ]
Mu, Limin [1 ,2 ]
Xu, Fei [1 ]
Zhang, Lu [1 ]
Wang, Jiancheng [1 ]
Zhang, Qiang [1 ,2 ]
机构
[1] Peking Univ, State Key Lab Nat & Biomimet Drugs, Beijing 100191, Peoples R China
[2] Shenyang Pharmaceut Univ, Sch Pharm, Shenyang 110016, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
anti-tumor medicine; cell carriers; molecular mechanisms; nanomedicines; targeting; tumor associated macrophages; ALBUMIN-BOUND PACLITAXEL; BREAST-CANCER; INFILTRATING MACROPHAGES; IMMUNE MICROENVIRONMENT; TARGETED DELIVERY; DRUG; NANOPARTICLES; LIPOSOMES; HYPOXIA; CELLS;
D O I
10.1002/adhm.202100590
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
As an important part of tumor microenvironment, tumor associated macrophages (TAMs) play a vital role in the occurrence, development, invasion, and metastasis of many malignant tumors and can significantly promote the formation of tumor blood vessels and lymphatic vessels, hence TAMs are greatly associated with poor prognosis. The research on nanomedicine has achieved huge progress, and nano-drugs have been widely utilized to treat various diseases through different mechanisms. Therefore, developing nano-drugs that are based on TAMs-associated anti-tumor mechanisms to effectively suppress tumor growth is expected to be a promising research filed. This paper introduces relevant information about TAMs in terms of their origin, and their roles in tumor genesis, development and metastasis. Furthermore, TAMs-related anti-tumor nano-drugs are summarized. Specifically, a wide range of nano-drugs targeting at TAMs are introduced, and categorized according to their therapeutic mechanisms toward tumors. Additionally, various nano delivery platforms using TAMs as cell carriers which aim at inhibiting tumor growth are reviewed. These two parts elucidate that the exploration of nanomedicine is essential to the study on TAMs-related anti-tumor strategies. This review is also intended to provide novel ideas for in-depth investigation on anti-tumor molecular mechanisms and nano-drug delivery systems based on TAMs.
引用
收藏
页数:21
相关论文
共 111 条
[1]   Mechanisms of phagocytosis in macrophages [J].
Aderem, A ;
Underhill, DM .
ANNUAL REVIEW OF IMMUNOLOGY, 1999, 17 :593-623
[2]  
Al-Sarireh B, 2000, J ROY COLL SURG EDIN, V45, P1
[3]   Role of therapeutic agents on repolarisation of tumour-associated macrophage to halt lung cancer progression [J].
Aldawsari, Hibah M. ;
Gorain, Bapi ;
Alhakamy, Nabil A. ;
Md, Shadab .
JOURNAL OF DRUG TARGETING, 2020, 28 (02) :166-175
[4]   The inflammatory micro-environment in tumor progression: The role of tumor-associated macrophages [J].
Allavena, Paola ;
Sica, Antonio ;
Solinas, Graziella ;
Porta, Chiara ;
Mantovani, Alberto .
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2008, 66 (01) :1-9
[5]  
[Anonymous], 2006, DRUG DISCOV TODAY
[6]   Nanomedicine Strategies to Target Tumor-Associated Macrophages [J].
Binnemars-Postma, Karin ;
Storm, Gert ;
Prakash, Jai .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2017, 18 (05)
[7]   Anti-Tumour Effects of Bisphosphonates - What have we Learned from In Vivo Models? [J].
Brown, H. K. ;
Holen, I. .
CURRENT CANCER DRUG TARGETS, 2009, 9 (07) :807-823
[8]   The Antitumor Efficacy of CpG Oligonucleotides is Improved by Encapsulation in Plant Virus-Like Particles [J].
Cai, Hui ;
Shukla, Sourabh ;
Steinmetz, Nicole F. .
ADVANCED FUNCTIONAL MATERIALS, 2020, 30 (15)
[9]   Metabolic modulation via mTOR pathway and anti-angiogenesis remodels tumor microenvironment using PD-L1-targeting codelivery [J].
Chen, Binfan ;
Gao, Ang ;
Tu, Bin ;
Wang, Yonghui ;
Yu, Xiaolu ;
Wang, Yingshu ;
Xiu, Yanfeng ;
Wang, Bing ;
Wan, Yakun ;
Huang, Yongzhuo .
BIOMATERIALS, 2020, 255
[10]   A nanoparticle-incorporated STING activator enhances antitumor immunity in PD-L1-insensitive models of triple-negative breast cancer [J].
Cheng, Ning ;
Watkins-Schulz, Rebekah ;
Junkins, Robert D. ;
David, Clement N. ;
Johnson, Brandon M. ;
Montgomery, Stephanie A. ;
Peine, Kevin J. ;
Darr, David B. ;
Yuan, Hong ;
Mckinnon, Karen P. ;
Liu, Qi ;
Miao, Lei ;
Huang, Leaf ;
Bachelder, Eric M. ;
Ainslie, Kristy M. ;
Ting, Jenny P-Y .
JCI INSIGHT, 2018, 3 (22)