Evidence map›Paper›PMID 39927632›Full record

ReviewCancer medicine2025

Tumor-Associated Macrophages: Key Players in the Non-Small Cell Lung Cancer Tumor Microenvironment.

Tongtong Lv, Rui Fan, Jiaqi Wu, Haolan Gong, Xiaoru Gao, Xin Liu, Yixin Gong, Bo Luo, Yanhua Zhang, Xiaochun Peng and 1 more

Abstract readReview
In one paragraph

Review in Cancer medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
–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

17 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  15. Smart nanoplatforms for early detection and immune modulation in lung cancer.Frontiers in bioengineering and biotechnology · 2025
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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

11 authors.

Tongtong LvDepartment of Hematology, The First Affiliated Hospital of Yangtze University, Jingzhou, China.
Rui FanDepartment of Hematology, The First Affiliated Hospital of Yangtze University, Jingzhou, China.
Jiaqi WuDepartment of Hematology, The First Affiliated Hospital of Yangtze University, Jingzhou, China.
Haolan GongDepartment of Hematology, The First Affiliated Hospital of Yangtze University, Jingzhou, China.
Xiaoru GaoDepartment of Hematology, The First Affiliated Hospital of Yangtze University, Jingzhou, China.
Xin LiuDepartment of Hematology, The First Affiliated Hospital of Yangtze University, Jingzhou, China.
Yixin GongDepartment of Hematology, The First Affiliated Hospital of Yangtze University, Jingzhou, China.
Bo LuoDepartment of Radiation Oncology, Hubei Cancer Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Yanhua ZhangDepartment of Hematology, The First Affiliated Hospital of Yangtze University, Jingzhou, China.
Xiaochun PengDepartment of Hematology, The First Affiliated Hospital of Yangtze University, Jingzhou, China.ORCID https://orcid.org/0000-0001-9443-0439
Gai LiangDepartment of Radiation Oncology, Hubei Cancer Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLung cancer is among the most common and deadliest malignant tumors worldwide. It is often detected at late stages, resulting in unfavorable outcomes, with tumor cell heterogeneity and medication resistance. Tumor-associated macrophages are among the key cells contributing to cancer progression. They are categorized into two primary phenotypes: Proinflammatory (M1) and anti-inflammatory (M2) which are involved in the onset and progression of NSCLC. The role of common cytokines secreted by macrophages in the progression of lung cancer are described, and the effects of various substances such as RNA or protein on the differentiation and polarization of two phenotypes of macrophages are highlighted to characterize the impact of the immune state of tumors on therapeutic effect of treatments and patient prognosis. Researchers have primarily aimed to investigate innovative carriers and strategies based on macrophages to modify the tumor microenvironment.

objectivesThese approaches are often integrated with other treatments, particularly immunotherapy, to enhance therapeutic efficacy.

methodsA comprehensive review was carried out by systematically synthesizing existing literature on PubMed, using the combination of the keywords "TAMs", "NSCLC", "Drug resistance", and "therapy". The available studies were screened for selection based on quality and relevance.

conclusionsTAMs promote tumor invasion, growth, and metastasis by promoting angiogenesis and EMT. In addition, they contribute to the development of drug resistance and the immunosuppressive microenvironment establishment. The immunosuppressive factors secreted by TAM can weaken the activity of immune cells, inhibit their killing effect on tumors, leading to immune suppression and hindering the effectiveness of treatment. Therefore, TAM is a key target for the development of cancer immunotherapy. Various strategies are being explored, including reducing the recruitment of TAMs and influencing their polarization to treat NSCLC. In addition, TAMs based treatment systems can achieve precise delivery of drugs or gene interfering molecules without causing side effects.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsTumor-Associated MacrophagesTumor MicroenvironmentAnimalsDrug Resistance, NeoplasmHumansImmunotherapybiomarkersdrug resistanceNSCLCTAMstreatment

Identifiers

PMID39927632
PMCPMC11808749

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Registered trials

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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.