Evidence map›Paper›PMID 25755696›Full record

ArticleInternational journal of clinical and experimental pathology2015

FOXA1 positively regulates gene expression by changing gene methylation status in human breast cancer MCF-7 cells.

Lu Zheng, Bo Qian, Duo Tian, Tong Tang, Shengyun Wan, Lei Wang, Lixin Zhu, Xiaoping Geng

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

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  6. Time-varying effects of FOXA1 on breast cancer prognosis.Breast cancer research and treatment · 2021
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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 1 institution in 1 country.

Lu ZhengDepartment of General Surgery, The Second Hospital of Anhui Medical University Anhui, Hefei 230601, China.
Bo QianDepartment of General Surgery, The Second Hospital of Anhui Medical University Anhui, Hefei 230601, China.
Duo TianDepartment of General Surgery, The Second Hospital of Anhui Medical University Anhui, Hefei 230601, China.
Tong TangDepartment of General Surgery, The Second Hospital of Anhui Medical University Anhui, Hefei 230601, China.
Shengyun WanDepartment of General Surgery, The Second Hospital of Anhui Medical University Anhui, Hefei 230601, China.
Lei WangDepartment of General Surgery, The Second Hospital of Anhui Medical University Anhui, Hefei 230601, China.
Lixin ZhuCental Laboratory, The First Hospital of Anhui Medical University Anhui, Hefei 230022, China.
Xiaoping GengDepartment of General Surgery, The Second Hospital of Anhui Medical University Anhui, Hefei 230601, China.
Anhui Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveDNA methylation is an important epigenetic modification with tumor suppressor gene silencing in cancer. The mechanisms underlying DNA methylation patterns are still poorly understood. This study aims to evaluate the potential value of FOXA1 for controlling gene CpG island methylation in breast cancer.

methodsFOXA1 was down-regulated by transfection with siRNA and up-regulated by transfection with plasmid in MCF-7 cell lines. The DNA methylation and mRNA levels were examined by qMSP and qRT-PCR. The cell proliferation and apoptosis was detected by MTT and Flow cytometry.

resultsSuppression of FOXA1 enhanced the methylation status of DAPK, MGMT, RASSF1A, p53, and depressed mRNA levels of these tumor suppressor genes, whereas over-expression of FOXA1 showed the opposite effects. DNMT1, DNMT3A and DNMT3B mRNA were up-regulated by siRNA knock-down of FOXA1. At the same time, FOXA1 suppression promoted cell growth and inhibited apoptosis.

conclusionsFOXA1 may be associated with methylation of the tumor suppressor genes promoter through changing DNMTs expression. FOXA1 could be a potential demethylation target for prevention and treatment of breast cancer.

Indexed as

Breast NeoplasmsDNA MethylationFlow CytometryGene Expression Regulation, NeoplasticHepatocyte Nuclear Factor 3-alphaHumansMCF-7 CellsReal-Time Polymerase Chain ReactionTransfectionFOXA1 protein, humanHepatocyte Nuclear Factor 3-alphaFOXA1MCF-7methylationtumor suppressor gene expression

Identifiers

PMID25755696
PMCPMC4348911
OpenAlexW125948116

What OpenQuestion holds

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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.