Evidence map›Paper›PMID 42046734›Full record

ReviewInternational journal of nanomedicine2026

Preclinical Nanoparticle Approaches Targeting Tumor-Associated Macrophages in Breast Cancer: From Mechanisms to Therapeutic Strategies.

Jiahui Teng, Xiaorong Zhang, Chunxiao Shen, Ling Wang, Jiali Hu, Zefen Li, Yan Liu, Jinyan Liu, Shufei Wei, Liangliang Wang

Abstract readReview
In one paragraph

Review in International journal of nanomedicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Jiahui TengThe First Clinical Medical School, Jiujiang University, Jiujiang, Jiangxi,People's Republic of China.
Xiaorong ZhangDepartment of Pathology, Affiliated Hospital of Jiujiang University, Jiujiang, Jiangxi, People's Republic of China.
Chunxiao ShenThe First Clinical Medical School, Jiujiang University, Jiujiang, Jiangxi,People's Republic of China.
Ling WangDepartment of Pathology, Affiliated Hospital of Jiujiang University, Jiujiang, Jiangxi, People's Republic of China.
Jiali HuDepartment of Pathology, Affiliated Hospital of Jiujiang University, Jiujiang, Jiangxi, People's Republic of China.
Zefen LiThe First Clinical Medical School, Jiujiang University, Jiujiang, Jiangxi,People's Republic of China.
Yan LiuDepartment of Pathology, Affiliated Hospital of Jiujiang University, Jiujiang, Jiangxi, People's Republic of China.
Jinyan LiuThe First Clinical Medical School, Jiujiang University, Jiujiang, Jiangxi,People's Republic of China.
Shufei WeiThe First Clinical Medical School, Jiujiang University, Jiujiang, Jiangxi,People's Republic of China.
Liangliang WangThe First Clinical Medical School, Jiujiang University, Jiujiang, Jiangxi,People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer is the most common malignancy among women worldwide, with high incidence and mortality rates. Tumor-associated macrophages (TAMs) are key mediators in the immunosuppressive tumor microenvironment (TME), contributing to poor prognosis and reducing immunotherapy efficacy. This review examines the dual roles of TAMs in breast cancer progression. TAMs are known to promote tumor development through angiogenesis, immune evasion, and metastasis, while M1-polarized TAMs conversely enhance antitumor immunity. Herein, the nanoparticle-based strategies targeting TAMs presented in preclinical research are explored, including reprogramming M2 to M1 macrophages, delivering MYC inhibitors, depleting TAMs, and inhibiting TAM recruitment. Integration with immune checkpoint inhibitors is also discussed. Challenges in translating these nanoparticle approaches from preclinical models to clinical practice are further addressed, with an emphasis placed on human-relevant models, optimized production processes, and personalized therapeutic approaches.

Indexed as

Breast NeoplasmsNanoparticlesTumor-Associated MacrophagesAnimalsAntineoplastic AgentsFemaleHumansImmune Checkpoint InhibitorsImmunotherapyMacrophagesTumor MicroenvironmentAntineoplastic AgentsImmune Checkpoint Inhibitorsbreast cancerimmune checkpoint inhibitorsM1/M2 Polarizationnanoparticlesnanotechnologytumor-associated macrophages

Identifiers

PMID42046734
PMCPMC13110746

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.