Evidence map›Paper›PMID 27518550›Full record

ArticleEye (London, England)2016

MicroRNA-125b promotes tumor growth and suppresses apoptosis by targeting DRAM2 in retinoblastoma.

S Bai, B Tian, A Li, Q Yao, G Zhang, F Li

Open access · bronzeAbstract read
In one paragraph

Article in Eye (London, England), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.2field-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

37 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
  2. Molecular insight into the therapeutic potential of miR-34a in retinoblastoma.Naunyn-Schmiedeberg's archives of pharmacology · 2025
    Review
  3. Review
  4. Article
  5. Integration of human stem cell-derivedFrontiers in cell and developmental biology · 2023
    Article
  6. Article
  7. The Clinical Spectrum and Disease Course of DRAM2 Retinopathy.International journal of molecular sciences · 2022
    Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  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

6 authors at 2 institutions in 1 country.

S BaiDepartment of Ophthalmology, Xi'an No.4 Hospital, Guangren Hospital of Xi'an Jiaotong University, Xi'an, China.
B TianDepartment of Ophthalmology, Xi'an No.4 Hospital, Guangren Hospital of Xi'an Jiaotong University, Xi'an, China.
A LiDepartment of Ophthalmology, First Hospital of Jilin University, Changchun, China.
Q YaoDepartment of Ophthalmology, Xi'an No.4 Hospital, Guangren Hospital of Xi'an Jiaotong University, Xi'an, China.
G ZhangDepartment of Ophthalmology, Xi'an No.4 Hospital, Guangren Hospital of Xi'an Jiaotong University, Xi'an, China.
F LiDepartment of Ophthalmology, Xi'an No.4 Hospital, Guangren Hospital of Xi'an Jiaotong University, Xi'an, China.
Xi'an Jiaotong University · CNJilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PurposeIt is known that microRNAs (miRNAs) are a class of small, noncoding RNAs that act as key regulators in various physiological and pathological processes. However, the regulatory mechanisms involving miRNAs in retinoblastoma (RB) remain largely unknown. The miRNA miR-125b is dysregulated in various human cancers such as breast cancer, human hepatocellular carcinoma, ovarian cancer, and colorectal cancer. However, the significance of miR-125b in RB has not been sufficiently investigated. Our objective was to explore the role of the miR-125b in RB.MethodsIn this study, we measured miR-125b levels using real-time polymerase chain reaction in human RB cell lines, including HXO-Rb44, Y79, SO-RB50, and the normal human retinal pigment epithelial cell line ARPE-19; a total of 38 pairs of primary RB tissues and adjacent noncancerous tissues were also measured. In addition, overexpression of miR-125b in RB cell lines was performed to determine the role of miR-125b in RB.ResultsWe found that miR-125b is significantly upregulated in RB, and closely associated with tumor cell proliferation and apoptosis. In addition, overexpression of miR-125b apparently promotes RB cell proliferation and migration in vitro. Gain-of-function in vitro experiments further showed that the miR-125b mimic significantly suppressed RB cell apoptosis. A subsequent dual-luciferase reporter assay identified the suppressor gene DRAM2 as direct target of miR-125b.ConclusionsOur data collectively demonstrate that miR-125b is a suppressor gene miRNA that can promote RB cell proliferation and migration by downregulating the suppressor gene DRAM2, indicating that miR-125b may represent a new potential diagnostic and therapeutic target for RB treatment.

Indexed as

ApoptosisBlotting, WesternCell Line, TumorCell MovementCell ProliferationHumansMembrane ProteinsMicroRNAsReal-Time Polymerase Chain ReactionRetinal Pigment EpitheliumRetinoblastomaRNA, MessengerUp-RegulationDRAM2 protein, humanMembrane ProteinsMicroRNAsMIRN125 microRNA, humanRNA, Messenger

Identifiers

PMID27518550
PMCPMC5177757
OpenAlexW2517638660

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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.