Evidence map›Paper›PMID 36435510›Full record

ArticleAging2022

Prognostic value and immunological role of FOXM1 in human solid tumors.

Guohua Wei, Xin Yang, Huangzhou Lu, Lan Zhang, Yong Wei, Hai Li, Mingxia Zhu, Xin Zhou

Open access · hybridAbstract read
In one paragraph

Article in Aging, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

7 citing papers in PubMed, 10 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 1 country.

Guohua WeiDepartment of Anesthesiology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.
Xin YangDepartment of Urology, The Second Affiliated Hospital of Nanjing Medical University, Nanjing 210000, China.
Huangzhou LuDepartment of Emergency, Changshu No.2 People's Hospital, The Fifth Affiliated Clinical Medical College of Yangzhou University, Changshu 215500, Jiangsu, China.
Lan ZhangDepartment of Radiation Oncology, Shanghai Tenth People's Hospital of Tongji University, Shanghai 200072, China.
Yong WeiDepartment of Urology, The Second Affiliated Hospital of Nanjing Medical University, Nanjing 210000, China.
Hai LiDepartment of Pathology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.
Mingxia ZhuDepartment of Radiation Oncology, The First Affiliated Hospital of Soochow University, Suzhou 215006, China.
Xin ZhouDepartment of Oncology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.
Nanjing Medical University · CNSecond Affiliated Hospital of Nanjing Medical University · CNJiangsu Province Hospital · CNSoochow University · CNTongji University · CNYangzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

FOXM1 acts as an oncogenic transcription factor and is involved in multiple hallmarks of human malignancies. Recent studies have demonstrated that FOXM1 is upregulated and correlated with poor prognosis in a majority of cancers. However, there are few pan-cancer analyses of FOXM1. This study aimed to investigate the expression profiles and clinical significance of FOXM1 in 31 types of solid tumors. We explored the expression profiles and the prognostic value of FOXM1 in pan-cancer across The Cancer Genome Atlas (TCGA). We further used lung adenocarcinoma (LUAD) tissues combined with quantitative real-time PCR (qRT-PCR) and immunohistochemistry (IHC) for experimental validation of FOXM1 expression. Besides, we verified the function of FOXM1 in a lung cancer cell line. Gene set enrichment analysis (GSEA) was conducted to explore signaling pathways related to FOXM1 expression. We observed that up-regulated FOXM1 was significantly related to poor survival in most tumors. Furthermore, there are significant correlations between FOXM1 expression and the infiltrating levels of different types of immune cells, TMB, MSI and immune checkpoint genes in a variety of cancers. Additional analysis based on IMvigor 210 cohort confirmed that patients with high level of FOXM1 exhibited a superior response to anti-PD-L1 therapy, and had a prolonged OS. In conclusion, this study indicated that FOXM1 could serve as a prognostic biomarker for most types of cancers and played a crucial role in the tumor immune microenvironment.

Indexed as

Lung NeoplasmsOncogenesCarcinogenesisForkhead Box Protein M1HumansPrognosisTumor MicroenvironmentForkhead Box Protein M1FOXM1 protein, humanFOXM1immune infiltrationpan-cancerprognosisTMB

Identifiers

PMID36435510
PMCPMC9740373
OpenAlexW4309754296

What OpenQuestion holds

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LicenceCC BY
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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.