Evidence map›Paper›PMID 38900063›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2024

In vitro functional assays to assess the reciprocal interplay between tumor cells and macrophages.

Adelya F Karimova, Avanee Ketkar, Roman Suezov, Adelya R Khalitova, Marina Gomzikova, Yana Mukhamedshina, Matthias Lauth, Magdalena Huber, Hans-Uwe Simon, Anna Brichkina

Abstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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.

Adelya F KarimovaInstitute of Fundamental Medicine and Biology, Kazan Federal University, Kazan, Russia.ORCID https://orcid.org/0000-0003-1388-2658
Avanee KetkarInstitute of Systems Immunology, Center for Tumor- and Immune Biology, Philipps University of Marburg, Marburg, Germany.ORCID https://orcid.org/0009-0002-1131-2723
Roman SuezovInstitute of Systems Immunology, Center for Tumor- and Immune Biology, Philipps University of Marburg, Marburg, Germany.ORCID https://orcid.org/0000-0001-6014-4338
Adelya R KhalitovaInstitute of Fundamental Medicine and Biology, Kazan Federal University, Kazan, Russia.ORCID https://orcid.org/0009-0004-9517-1693
Marina GomzikovaInstitute of Fundamental Medicine and Biology, Kazan Federal University, Kazan, Russia.ORCID https://orcid.org/0000-0002-0826-7370
Yana MukhamedshinaInstitute of Fundamental Medicine and Biology, Kazan Federal University, Kazan, Russia.ORCID https://orcid.org/0000-0002-9435-340X
Matthias LauthDepartment of Gastroenterology, Endocrinology and Metabolism, Center for Tumor- and Immune Biology, Philipps University of Marburg, Marburg, Germany.ORCID https://orcid.org/0000-0001-5922-5384
Magdalena HuberInstitute of Systems Immunology, Center for Tumor- and Immune Biology, Philipps University of Marburg, Marburg, Germany.ORCID https://orcid.org/0000-0002-2963-0693
Hans-Uwe SimonInstitute of Fundamental Medicine and Biology, Kazan Federal University, Kazan, Russia.ORCID https://orcid.org/0000-0002-9404-7736
Anna BrichkinaInstitute of Fundamental Medicine and Biology, Kazan Federal University, Kazan, Russia.ORCID https://orcid.org/0000-0001-8707-9900

Funding

Deutsche Forschungsgemeinschaft (DFG) BR 5749/1-1Deutsche José Carreras Leukämie-Stiftung e.V. 14R/2020Deutsche José Carreras Leukämie-Stiftung e.V. 19R/2023Russian Government Programm 075-15-2021-600Swiss National Science Foundation 310030_184816Universitätsklinikum Giessen und Marburg 2/2019 MR
6 · The paper itself

Abstract

Tumor-associated macrophages (TAMs) are integral components of the tumor microenvironment. They are involved in various aspects of tumor cell biology, driving pathological processes such as tumor cell proliferation, metastasis, immunosuppression, and resistance to therapy. TAMs exert their tumorigenic effects by secreting growth factors, cytokines/chemokines, metabolites, and other soluble bioactive molecules. These mediators directly promote tumor cell proliferation and modulate interactions with immune and stromal cells, facilitating further tumor growth. As research into therapies targeting TAMs intensifies, there is a growing need for reliable methods to comprehend the impact of TAMs on cancer progression and to validate novel therapeutics directed at TAMs. The traditional "M1-M2" macrophage classification based on transcriptional profiles of TAMs is not only too simplistic to describe their physiological roles, it also does not explain differences observed between mouse and human macrophages. In this context, methods that assess how TAMs influence tumor or immune cells, either through direct contact or the release of soluble factors, offer a more promising approach. We describe here comprehensive protocols for in vitro functional assays to study TAMs, specifically regarding their impact on the growth of lung cancer cells. We have applied these methods to both mouse and human macrophages, achieving similar outcomes in promoting the proliferation of cancer cells. This methodology can serve as a standardized approach for testing novel therapeutic approaches, targeting TAMs with novel immunotherapeutic compounds, or utilizing gene-editing techniques. Taken together, the described methodology may contribute to our understanding of complex macrophage-tumor interactions and support the development of innovative therapeutic strategies.

Indexed as

Tumor-Associated MacrophagesTumor MicroenvironmentAnimalsCell Line, TumorCell ProliferationHumansLung NeoplasmsMacrophagesMiceNeoplasms

Identifiers

PMID38900063
PMCPMC13688220

What OpenQuestion holds

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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.