Evidence map›Paper›PMID 37058885›Full record

ArticleNeoplasia (New York, N.Y.)2023

Hepatocellular carcinoma-derived FOXO1 inhibits tumor progression by suppressing IL-6 secretion from macrophages.

Xiao Cui, Huiyong Zhao, Sheng Wei, Qiang Du, Kun Dong, Yihe Yan, David A Geller

Open access · goldAbstract read
In one paragraph

Article in Neoplasia (New York, N.Y.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
3.5field-weighted citation impact, top 7% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

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  11. The Role of Interferon Regulatory Factors in Liver Diseases.International journal of molecular sciences · 2024
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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 4 institutions in 2 countries.

Xiao CuiDepartment of General Surgery, The Second Hospital of Anhui Medical University, Hefei, Anhui, 230601, China; Department of Surgery, University of Pittsburgh Medical Center, Pittsburgh, PA, 15260, USA. Electronic address: cx_2077@bjmu.edu.cn.
Huiyong ZhaoDepartment of General Surgery, The Second Hospital of Anhui Medical University, Hefei, Anhui, 230601, China. Electronic address: drzhy2020@163.com.
Sheng WeiDepartment of General Surgery, The Second Hospital of Anhui Medical University, Hefei, Anhui, 230601, China. Electronic address: ws940803@163.com.
Qiang DuDepartment of Surgery, University of Pittsburgh Medical Center, Pittsburgh, PA, 15260, USA. Electronic address: qiangdu@pitt.edu.
Kun DongDepartment of Pediatric Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, 530021, China. Electronic address: dongkun007@163.com.
Yihe YanDepartment of General Surgery, The Second Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, 530007, China. Electronic address: yanyihe12@sr.gxmu.edu.cn.
David A GellerDepartment of Surgery, University of Pittsburgh Medical Center, Pittsburgh, PA, 15260, USA. Electronic address: gellerda@upmc.edu.
Anhui Medical University · CNUniversity of Pittsburgh Medical Center · USFirst Affiliated Hospital of GuangXi Medical University · CNGuangxi Medical University · CN

Funding

NLM NIH HHS HHSN276201200017C
6 · The paper itself

Abstract

Tumor heterogeneity dominates tumor biological behavior and shapes the tumor microenvironment. However, the mechanisms of tumor genetic features modulate immunity response were not clearly clarified. Tumor associated macrophages (TAMs) exert distinct immune functions in the progression of hepatocellular carcinoma (HCC) based on the inducible phenotype. FOXO family members sense changes in the extracellular or intracellular environment by activating a series of signaling pathways. FOXO1, a transcription factor that a common suppressor in hepatocellular carcinoma, correlated with a better tumor biological behavior in HCC through shaping macrophages anti-tumour response. Here, we found that human HCC tissue microarray (TMA) slides were employed to showed tumor derived FOXO1 negatively related with distribution of protumour macrophages. This phenomenon was confirmed in mouse xenograft model and in vitro. HCC-derived FOXO1 inhibits tumorigenesis not only by targeting tumor cells but also by synchronizing with re-educated macrophages. These effects may be partially dependent on FOXO1 transcriptionally modulates IRF-1/nitrio oxide (NO) axis in exerting effects in macrophages and decreasing IL-6 releasing from macrophages in tumor microenvironment indirectly. This feedback suppressed the progression of HCC by inactivation of IL-6/STAT3 in HCC. It implicates the potential role of FOXO1 in the therapeutic effects for modulating immune response by targeting macrophages.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsAnimalsCell Line, TumorForkhead Box Protein O1HumansInterleukin-6MacrophagesMiceSignal TransductionTumor MicroenvironmentForkhead Box Protein O1FOXO1 protein, humanIL6 protein, humanInterleukin-6FOXO1Hepatocellular carcinomaInflammationMacrophages

Identifiers

PMID37058885
PMCPMC10123375
OpenAlexW4365152614

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.