Evidence map›Paper›PMID 32840296›Full record

Observational studyBioscience reports2020

MiR-940 promotes malignant progression of breast cancer by regulating FOXO3.

Huayao Zhang, Jingwen Peng, Jianguo Lai, Haiping Liu, Zhiyuan Zhang, Xiangdi Li, Baozhen Liang, Xuejun Chen, Baojia Zou, Siyuan Lin and 1 more

Abstract readObservational Study
In one paragraph

Observational study in Bioscience reports, 2020. 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
–field-weighted citation impact
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.

  1. Article
  2. The Role of the Fox Gene in Breast Cancer Progression.International journal of molecular sciences · 2025
    Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. LncRNACancers · 2022
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Differential Expression andIndian journal of dermatology
    Article
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

11 authors.

Huayao Zhang *Breast thyroid surgery department, SSL Central Hospital of Dongguan City, Dongguan 523326, Guangdong Province, China.
Jingwen Peng *Department of Rehabilitation Medicine, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou 510120, Guangdong Province, China.
Jianguo Lai *Department of Breast Cancer, Cancer Center, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou 510000, Guangdong Province, China.
Haiping LiuBreast thyroid surgery department, SSL Central Hospital of Dongguan City, Dongguan 523326, Guangdong Province, China.
Zhiyuan ZhangBreast thyroid surgery department, SSL Central Hospital of Dongguan City, Dongguan 523326, Guangdong Province, China.
Xiangdi LiBreast thyroid surgery department, SSL Central Hospital of Dongguan City, Dongguan 523326, Guangdong Province, China.
Baozhen LiangBreast thyroid surgery department, SSL Central Hospital of Dongguan City, Dongguan 523326, Guangdong Province, China.
Xuejun ChenBreast thyroid surgery department, SSL Central Hospital of Dongguan City, Dongguan 523326, Guangdong Province, China.
Baojia ZouDepartment of Hepatobiliary Surgery, The Fifth Affiliated Hospital, Sun Yat-sen University, Zhuhai 519000, Guangdong Province, China.
Siyuan LinBreast thyroid surgery department, SSL Central Hospital of Dongguan City, Dongguan 523326, Guangdong Province, China.
Lihua ZhangBreast thyroid surgery department, SSL Central Hospital of Dongguan City, Dongguan 523326, Guangdong Province, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer (BC) is a common cancer with poor survival. The present study aimed to explore the effect of miR-940 on the process of BC cells and its target gene FOXO3. The expression of miR-940 was assessed in BC tissues and cells using qRT-PCR. Furthermore, the correlation between miR-940 and prognosis of BC patients from the TCGA database was analyzed. CCK8 assays and colony formation assays were used to explore the effect of miR-940 on BC cell proliferation. The invasion abilities were detected by transwell assays. Luciferase reporter assay was performed to scrutinize the relationship between miR-940 and FOXO3. Finally, rescue experiments were performed through FOXO3 down-regulation and miR-940 inhibitors by using CCK8 assays, colony formation assays and transwell assays. miR-940 was significantly up-regulated in BC cells and tissues. In addition, the high level of miR-940 correlated with poor survival of BC patients (P=0.023). CCK8 assays, colony formation assays and transwell assays indicated that miR-940 promoted the proliferation and invasion abilities of BC cells. The luciferase reporter assay suggested that miR-940 directly targeted FOXO3. Moreover, we found that the effect of si-FOXO3 was rescued by miR-940 inhibitors in BC cells. miR-940 may promote the proliferation and invasion abilities of BC cells by targeting FOXO3. Our study suggested that miR-940 could be a novel molecular target for therapies against BC.

Indexed as

Gene Expression Regulation, NeoplasticAdultAgedBiomarkers, TumorBreastBreast NeoplasmsCell Line, TumorCell MovementCell ProliferationDisease ProgressionFemaleForkhead Box Protein O3HumansKaplan-Meier EstimateMastectomyMicroRNAsBiomarkers, TumorForkhead Box Protein O3FOXO3 protein, humanMicroRNAsMIRN940 microRNA, humanBreast cancerFOXO3miR-940

Identifiers

PMID32840296
PMCPMC7494982

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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.