Evidence map›Paper›PMID 31638197›Full record

ArticleMolecular medicine reports2019

miR‑222 induces apoptosis in human intervertebral disc nucleus pulposus cells by targeting Bcl‑2.

Wei Wang, Jian Wang, Jiayi Zhang, Wei Taq, Zhenxing Zhang

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

12 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Mechanobiology of MicroRNAs in Intervertebral Disk Degeneration.Journal of spine research and surgery · 2023
    Article
  5. Review
  6. Review
  7. Panax notoginseng saponin reducesAnnals of translational medicine · 2022
    Article
  8. MiR-206 improves intervertebral disk degeneration by targeting GJA1.Journal of orthopaedic surgery and research · 2022
    Article
  9. Review
  10. M1 macrophage-derived exosomes transfer miR-222 to induce bone marrow mesenchymal stem cell apoptosis.Laboratory investigation; a journal of technical methods and pathology · 2021
    Article
  11. Article
  12. 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

5 authors at 1 institution in 1 country.

Wei WangDepartment of Rehabilitation, The First Affiliated Hospital of Jinzhou Medical University, Jinzhou, Liaoning 121000, P.R. China.
Jian WangDepartment of Orthopedics, The First Affiliated Hospital of Jinzhou Medical University, Jinzhou, Liaoning 121000, P.R. China.
Jiayi ZhangDepartment of Orthopedics, The First Affiliated Hospital of Jinzhou Medical University, Jinzhou, Liaoning 121000, P.R. China.
Wei TaqDepartment of General Surgery, The First Affiliated Hospital of Jinzhou Medical University, Jinzhou, Liaoning 121000, P.R. China.
Zhenxing ZhangDepartment of Neurosurgery, The First Affiliated Hospital of Jinzhou Medical University, Jinzhou, Liaoning 121000, P.R. China.
Jinzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intervertebral disc degeneration (IDD) is characterized by abnormal induction of apoptosis in intervertebral disc nucleus pulposus (NP) cells. Previous studies indicated that miR‑222 was upregulated in patients with rheumatoid arthritis. However, the effects of miR‑222 in IDD remain unclear. The present study aimed to demonstrate the role of miR‑222 in NP cells. The levels of miR‑222 in patients with IDD were measured by reverse transcription‑quantitative PCR. Cell Counting Kit‑8 and western blotting assays were used to detect cell proliferation and apoptosis‑associated protein levels, respectively. In addition, luciferase reporter assays were performed to validate the predicted target genes of miR‑222. miR‑222 was significantly upregulated in patients with IDD. Overexpression of miR‑222 inhibited cell proliferation and induced cell apoptosis. Moreover, overexpression of miR‑222 resulted in an upregulation in the levels of Bax and cleaved caspase 3, and a downregulation in the levels of Bcl‑2 in NP cells. The luciferase reporter assays demonstrated that Bcl‑2 is a target of miR‑222. Furthermore, overexpression of miR‑222 increased the levels of cytochrome c, apoptotic protease activating factor‑1 and cleaved caspase 9 in NP cells. Conversely, downregulation of miR‑222 could promote the proliferation of NP cells. The present data demonstrated that miR‑222 induced apoptosis in NP cells by directly targeting Bcl‑2. Therefore, miR‑222 may act as a potential therapeutic target for the treatment of IDD.

Indexed as

ApoptosisAdultAgedCell LineDown-RegulationFemaleHumansIntervertebral DiscIntervertebral Disc DegenerationMaleMicroRNAsMiddle AgedNucleus PulposusProto-Oncogene Proteins c-bcl-2Up-RegulationMicroRNAsMIR222, humanProto-Oncogene Proteins c-bcl-2

Identifiers

PMID31638197
PMCPMC6854584
OpenAlexW2979997516

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.