Evidence map›Paper›PMID 35975458›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2022

FOXM1 Inhibition Enhances the Therapeutic Outcome of Lung Cancer Immunotherapy by Modulating PD-L1 Expression and Cell Proliferation.

Hamadi Madhi, Jeon-Soo Lee, Young Eun Choi, Yan Li, Myoung Hee Kim, Yongdoo Choi, Sung-Ho Goh

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 1 pooled it
6.6field-weighted citation impact, top 2% 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

57 citing papers in PubMed, 1 synthesis or guideline pooled it, 78 citations in OpenAlex.

  1. Antibiotic adoption effects on nutrition and quality of life in lung cancer patients undergoing radiotherapy and chemotherapy: A meta-analysis.Technology and health care : official journal of the European Society for Engineering and Medicine · 2024
    Pooled it
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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

7 authors at 2 institutions in 1 country.

Hamadi MadhiResearch Institute, National Cancer Center, 323 Ilsan-ro, Goyang, Gyeonggi-Do, 10408, Republic of Korea.
Jeon-Soo LeeResearch Institute, National Cancer Center, 323 Ilsan-ro, Goyang, Gyeonggi-Do, 10408, Republic of Korea.
Young Eun ChoiResearch Institute, National Cancer Center, 323 Ilsan-ro, Goyang, Gyeonggi-Do, 10408, Republic of Korea.
Yan LiResearch Institute, National Cancer Center, 323 Ilsan-ro, Goyang, Gyeonggi-Do, 10408, Republic of Korea.
Myoung Hee KimDepartment of Anatomy, Graduate School of Medical Sciences, Yonsei University College of Medicine, Seoul, 03722, Republic of Korea.
Yongdoo ChoiResearch Institute, National Cancer Center, 323 Ilsan-ro, Goyang, Gyeonggi-Do, 10408, Republic of Korea.ORCID 0000-0003-4231-6946
Sung-Ho GohResearch Institute, National Cancer Center, 323 Ilsan-ro, Goyang, Gyeonggi-Do, 10408, Republic of Korea.
National Cancer Center · KRYonsei University · KR

Funding

National Cancer Center 2110540National Cancer Center 2210721
6 · The paper itself

Abstract

Programmed death-ligand 1 (PD-L1) is a major target to cancer immunotherapy, and anti-PD-L1 and anti-PD-1 antibody-mediated immunotherapy are being increasingly used. However, immune checkpoint inhibitors (ICIs) are ineffective in treating large tumors and cause various immune-related adverse events in nontarget organs, including life-threatening cardiotoxicity. Therefore, the development of new therapeutic strategies to overcome these limitations is crucial. The focus of this study is the forkhead box protein M1 (FOXM1), which is identified as a potential therapeutic target for cancer immunotherapy and is associated with the modulation of PD-L1 expression. Selective small interfering RNA knockdown of FOXM1 or treatment with thiostrepton (TST) significantly reduces PD-L1 expression in non-small-cell lung cancer (NSCLC) cells and inhibits proliferation. Chromatin immunoprecipitation-PCR reveals that FOXM1 selectively upregulates PD-L1 expression by binding directly to the PD-L1 promoter. In vivo animal studies have shown that TST treatment significantly downregulates PD-L1 expression in human NSCLC tumors, while greatly reducing tumor size without side effects on normal tissues. Combined treatment with TST and anti-4-1BB antibody in the LLC-1 syngeneic tumor model induces synergistic therapeutic outcomes against immune resistant lung tumors as well as 2.72-folds higher CD3

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsAnimalsB7-H1 AntigenCell ProliferationForkhead Box Protein M1HumansImmune Checkpoint InhibitorsImmunotherapyProgrammed Cell Death 1 ReceptorRNA, Small InterferingThiostreptonTreatment OutcomeB7-H1 AntigenCD274 protein, humanForkhead Box Protein M1FOXM1 protein, humanImmune Checkpoint InhibitorsProgrammed Cell Death 1 ReceptorRNA, Small InterferingThiostreptonforkhead box protein M1immunotherapylung cancerprogrammed death-ligand 1thiostrepton

Identifiers

PMID35975458
PMCPMC9561767
OpenAlexW4292260712

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.