Evidence map›Paper›PMID 36798830›Full record

ReviewFrontiers in oncology2023

Interleukin-34 and immune checkpoint inhibitors: Unified weapons against cancer.

Fadhl Alshaebi, Mohammed Safi, Yousif A Algabri, Mahmoud Al-Azab, Abdullah Aldanakh, Mohammed Alradhi, Alariqi Reem, Caiqing Zhang

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.8field-weighted citation impact, top 9% of its field
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

5 citing papers in PubMed, 12 citations in OpenAlex.

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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

8 authors at 6 institutions in 2 countries.

Fadhl AlshaebiDepartment of Respiratory, Shandong Second Provincial General Hospital, Shandong University, Jinan, Shandong, China.
Mohammed SafiDepartment of Respiratory, Shandong Second Provincial General Hospital, Shandong University, Jinan, Shandong, China.
Yousif A AlgabriDepartment of Biomedical Engineering, School of Control Science and Engineering, Shandong University, Jinan, Shandong, China.
Mahmoud Al-AzabDepartment of Immunology, Guangzhou Institute of Pediatrics, Guangzhou Women and Children's Medical Center, Guangdong Provincial Clinical Research Center for Child Health, Guangzhou Medical University, Guangzhou, China.
Abdullah AldanakhDepartment of Urology, First Affiliated Hospital of Dalian Medical University, Dalian, Liaoning, China.
Mohammed AlradhiDepartment of Urology, The Affiliated Hospital of Qingdao Binhai University, Qingdao, Shandong, China.
Alariqi ReemFaculty of Medicine and Health Sciences, Amran University, Amran, Yemen.
Caiqing ZhangDepartment of Respiratory, Shandong Second Provincial General Hospital, Shandong University, Jinan, Shandong, China.
Second Hospital of Shandong University · CNAmran University · YEDalian Medical University · CNGuangzhou Medical University · CNQingdao University · CNShandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interleukin-34 (IL-34) is a cytokine that is involved in the regulation of immune cells, including macrophages, in the tumor microenvironment (TME). Macrophages are a type of immune cell that can be found in large numbers within the TME and have been shown to have a role in the suppression of immune responses in cancer. This mmune suppression can contribute to cancer development and tumors' ability to evade the immune system. Immune checkpoint inhibitors (ICIs) are a type of cancer treatment that target proteins on immune cells that act as "checkpoints," regulating the activity of the immune system. Examples of these proteins include programmed cell death protein 1 (PD-1) and cytotoxic T-lymphocyte-associated protein 4 (CTLA-4). ICIs work by blocking the activity of these proteins, allowing the immune system to mount a stronger response against cancer cells. The combination of IL-34 inhibition with ICIs has been proposed as a potential treatment option for cancer due to the role of IL-34 in the TME and its potential involvement in resistance to ICIs. Inhibiting the activity of IL-34 or targeting its signaling pathways may help to overcome resistance to ICIs and improve the effectiveness of these therapies. This review summarizes the current state of knowledge concerning the involvement of IL-34-mediated regulation of TME and the promotion of ICI resistance. Besides, this work may shed light on whether targeting IL-34 might be exploited as a potential treatment option for cancer patients in the future. However, further research is needed to fully understand the mechanisms underlying the role of IL-34 in TME and to determine the safety and efficacy of this approach in cancer patients.

Indexed as

cancer therapycytotoxic T-lymphocyte-associated protein 4 (CTLA-4)immune checkpoint inhibitors (ICIs)interluikin-34 (IL-34)programmed cell death protein 1 (PD-1)tumor microenvironment

Identifiers

PMID36798830
PMCPMC9927403
OpenAlexW4318592090

What OpenQuestion holds

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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.