Evidence map›Paper›PMID 33008330›Full record

ArticleBMC cancer2020

Oncogenic miR-20b-5p contributes to malignant behaviors of breast cancer stem cells by bidirectionally regulating CCND1 and E2F1.

Liqin Xia, Feng Li, Jun Qiu, Zhongming Feng, Zihan Xu, Zhengtang Chen, Jianguo Sun

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

24 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Article
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  5. Review
  6. Article
  7. Exploring the time-dependent regulatory potential of microRNAs in breast cancer cells treated with proteasome inhibitors.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
    Article
  8. Review
  9. Review
  10. Effect ofMicroorganisms · 2023
    Article
  11. The dual role of microRNA (miR)-20b in cancers: Friend or foe?Cell communication and signaling : CCS · 2023
    Review
  12. Article
  13. Article
  14. Review
  15. Mitochondrial micropeptide STMP1 promotes G1/S transition by enhancing mitochondrial complex IV activity.Molecular therapy : the journal of the American Society of Gene Therapy · 2022
    Article
  16. Article
  17. Review
  18. HepaticeLife · 2021
    Article
  19. Review
  20. 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

7 authors at 3 institutions in 1 country.

Liqin XiaInstitute of Cancer, Xinqiao Hospital, Army Medical University, Chongqing, 400037, China.
Feng LiInstitute of Cancer, Xinqiao Hospital, Army Medical University, Chongqing, 400037, China.
Jun QiuXiamen Humanity Hospital Fujian Medical University, Xiamen, 361000, Fujian, China.
Zhongming FengInstitute of Cancer, Xinqiao Hospital, Army Medical University, Chongqing, 400037, China.
Zihan XuInstitute of Cancer, Xinqiao Hospital, Army Medical University, Chongqing, 400037, China.
Zhengtang ChenInstitute of Cancer, Xinqiao Hospital, Army Medical University, Chongqing, 400037, China.
Jianguo SunInstitute of Cancer, Xinqiao Hospital, Army Medical University, Chongqing, 400037, China. sunjg09@aliyun.com.
Army Medical University · CNXinqiao Hospital · CNFujian Medical University · CN

Funding

National Natural Science Foundation of China 30772108National Natural Science Foundation of China 81272910Natural Science Foundation of Chongqing cstc2012jjB10003
6 · The paper itself

Abstract

backgroundBreast cancer is the leading cause of cancer mortality in women worldwide. Therefore, it is of great significance to identify the biological mechanism of tumorigenesis and explore the development of breast cancer to achieve a better prognosis for individuals suffering from breast cancer. MicroRNAs (miRNAs) have become a hot topic in cancer research, but the underlying mechanism of its involvement in cancer remains unclear.

methodsThe miRNA profile between breast cancer stem cells (BCSCs, CD44

resultsMiR-20b-5p had the highest degree in both the miRNA-gene network and miRNA-GO network to regulate BCSCs. Overexpression of miR-20b-5p significantly promoted the migration and wound healing ability of MCF-7 cells and T47D cells compared with the control (P < 0.05). In addition, miR-20b-5p facilitated the proliferation of MCF-7 cells and T47D-CSCs (P < 0.05) and inhibited the apoptosis of T47D-CSCs (P < 0.05). Moreover, miR-20b-5p promoted xenograft growth compared with the control group (P < 0.05). Accordingly, potential targets of both CCND1 and E2F1 were predicted by bioinformatics analysis. MiR-20b-5p directly targeted both CCND1 and E2F1 in a dual luciferase assay, while antagomir-20b-5p downregulated the protein levels of CCND1 and E2F1.

conclusionsOncogenic miR-20b-5p was confirmed to promote the malignant behaviors of breast cancer cells and BCSCs. The underlying mechanism lies in that miR-20b-5p overall enhanced both CCND1 and E2F1 targets via bidirectional regulation probably involving direct downregulation and indirect upregulation.

Indexed as

AnimalsBreast NeoplasmsCell ProliferationCyclin D1E2F1 Transcription FactorFemaleHumansMiceMice, NudeNeoplastic Stem CellsOncogenesTransfectionCCND1 protein, humanCyclin D1E2F1 protein, humanE2F1 Transcription FactorBidirectional regulationBreast cancerCancer stem cellsCCND1E2F1miR-20b-5p

Identifiers

PMID33008330
PMCPMC7531112
OpenAlexW3090659807

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.