Evidence map›Paper›PMID 27186302›Full record

ArticleAmerican journal of translational research2016

miR-141 modulates osteoblastic cell proliferation by regulating the target gene of lncRNA H19 and lncRNA H19-derived miR-675.

Peiheng He, Ziji Zhang, Guangxin Huang, Hua Wang, Dongliang Xu, Weiming Liao, Yan Kang

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

27 citing papers in PubMed, 51 citations in OpenAlex.

  1. Review
  2. Review
  3. Long noncoding RNA (lncRNA)Genes & diseases · 2023
    Review
  4. Article
  5. Article
  6. Article
  7. Role ofFrontiers in genetics · 2021
    Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
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  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Interaction and cross-talk between non-coding RNAs.Cellular and molecular life sciences : CMLS · 2018
    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 1 institution in 1 country.

Peiheng HeDepartment of Joint Surgery, The First Affiliated Hospital of Sun Yat-sen University Guangzhou 510080, China.
Ziji ZhangDepartment of Joint Surgery, The First Affiliated Hospital of Sun Yat-sen University Guangzhou 510080, China.
Guangxin HuangDepartment of Joint Surgery, The First Affiliated Hospital of Sun Yat-sen University Guangzhou 510080, China.
Hua WangDepartment of Joint Surgery, The First Affiliated Hospital of Sun Yat-sen University Guangzhou 510080, China.
Dongliang XuDepartment of Joint Surgery, The First Affiliated Hospital of Sun Yat-sen University Guangzhou 510080, China.
Weiming LiaoDepartment of Joint Surgery, The First Affiliated Hospital of Sun Yat-sen University Guangzhou 510080, China.
Yan KangDepartment of Joint Surgery, The First Affiliated Hospital of Sun Yat-sen University Guangzhou 510080, China.
Sun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Increasing evidence has reported the significant roles of lncRNA or miRNAs in the biology of various diseases. This study was aimed to elucidate the potential roles of miR-141 and lncRNA H19 and H19-derived miR-675 in regulating osteoblasts proliferation and apoptosis and to explore its potential mechanism. miR-141 mimic or miR-141 inhibitor or siRNA-H19 or miR-675 inhibitor was transfected into human hFOB1.19 cells. The effects or miR-141 expression on H19 or miR-675 expression, on osteoblasts proliferation and apoptosis were analyzed. Moreover, effects of H19 and miR-675 expression on cell proliferation were also analyzed. The results showed that miR-141 was down-regulated in both hFOB1.19 cells and osteosarcoma tissues. The overexpressed miR-141 suppressed H19 and miR-675 expression in hFOB1.19 cells. Besides, miR-141 suppression significantly increased cell viability but this effect was blocked by silencing H19 or miR-675 inhibitor, which is similar to the effects on VEGF and IGF2 expression. Furthermore, miR-141 overexpression induced osteoblasts apoptosis, but decreased the levels of caspase-3 and the Bcl-2/Bax ratio. Taken together, our study revealed that tumor-suppressor miR-141 overexpression suppressed osteoblasts proliferation but induced apoptosis through down-regulating H19 or miR-675 in osteosarcoma. This study may provide theoretical basis for illustrating the interaction between lncRNA and miRNAs in osteosarcoma and for the therapeutic target of miR-141 in osteosarcoma treatment.

Indexed as

cell proliferationlncRNA H19lncRNA H19-derived miR-675miR-141Osteoblasts

Identifiers

PMID27186302
PMCPMC4859907
OpenAlexW2398901947

What OpenQuestion holds

Textmetadata
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.