Evidence map›Paper›PMID 38448802›Full record

ArticleBMC genomics2024

Integrated analysis reveals FLI1 regulates the tumor immune microenvironment via its cell-type-specific expression and transcriptional regulation of distinct target genes of immune cells in breast cancer.

Jianying Pei, Ying Peng, Kexin Ma, Chunyan Lan, Tingting Zhang, Yan Li, Xiaofang Chen, Huafang Gao

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 12% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
  2. International journal of molecular medicine · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. LncRNA CKMT2-AS1 Promotes Hepatocellular Carcinoma Development Via Sponging miR-142-5p and Targeting IFITM3.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2025
    Article
  8. Review
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 4 institutions in 1 country.

Jianying PeiNational Research Institute for Family Planning, Beijing, 100081, China.
Ying PengDepartment of General Surgery, Peking University Third Hospital, Beijing, 100191, China.
Kexin MaNational Research Institute for Family Planning, Beijing, 100081, China.
Chunyan LanNational Research Institute for Family Planning, Beijing, 100081, China.
Tingting ZhangMedical College of Northwest Minzu University, Lanzhou, 730030, China.
Yan LiMedical College of Northwest Minzu University, Lanzhou, 730030, China.
Xiaofang ChenSchool of Biological Science and Medical Engineering, Beihang University, Beijing, 100083, China. xfchen@buaa.edu.cn.
Huafang GaoNational Research Institute for Family Planning, Beijing, 100081, China. gaohuafang@nrifp.org.cn.
Minzu University of China · CNTianjin Municipal Research Institute for Family Planning · CNPeking Union Medical College Hospital · CNPeking University · CN

Funding

the Lanzhou Science and Technology Bureau 2022-ZD-62the Natural Science Foundation of Gansu Province 22JR5RA191the Natural Science Foundation of Gansu Province 23JRRA1381
6 · The paper itself

Abstract

backgroundImmunotherapy is a practical therapeutic approach in breast cancer (BRCA), and the role of FLI1 in immune regulation has gradually been unveiled. However, the specific role of FLI1 in BRCA was conflicted; thus, additional convincing evidence is needed.

methodsWe explored the upstream regulation of FLI1 expression via summary data-based Mendelian randomization (SMR) analysis and ncRNA network construction centering on FLI1 using BRCA genome-wide association study (GWAS) summary data with expression quantitative trait loci (eQTLs) and DNA methylation quantitative trait loci (mQTLs) from the blood and a series of in silico analyses, respectively. We illuminated the downstream function of FLI1 in immune regulation by integrating a series of analyses of single-cell RNA sequence data (scRNA-seq).

resultsWe verified a causal pathway from FLI1 methylation to FLI1 gene expression to BRCA onset and demonstrated that FLI1 was downregulated in BRCA. FLI1, a transcription factor, served as myeloid and T cells' communication regulator by targeting immune-related ligands and receptor transcription in BRCA tissues. We constructed a ceRNA network centering on FLI1 that consisted of three LncRNAs (CKMT2-AS1, PSMA3-AS1, and DIO3OS) and a miRNA (hsa-miR-324-5p), and the expression of FLI1 was positively related to a series of immune-related markers, including immune cell infiltration, biomarkers of immune cells, and immune checkpoints.

conclusionLow-methylation-induced or ncRNA-mediated downregulation of FLI1 is associated with poor prognosis, and FLI1 might regulate the tumor immune microenvironment via a cell-type-specific target genes manner in BRCA.

Indexed as

MicroRNAsNeoplasmsCreatine Kinase, Mitochondrial FormGene Expression RegulationGenome-Wide Association StudyHumansMicrofilament ProteinsQuantitative Trait LociTrans-ActivatorsTranscription FactorsTumor MicroenvironmentCKMT2 protein, humanCreatine Kinase, Mitochondrial FormFLII protein, humanMicrofilament ProteinsMicroRNAsMIRN324 microRNA, humanTrans-ActivatorsTranscription FactorsBreast cancerCell communicationFLI1Immune cellsscRNA-seqTranscription factor

Identifiers

PMID38448802
PMCPMC10916124
OpenAlexW4392517227

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LicenceCC BY
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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.