Evidence map›Paper›PMID 31392505›Full record

ArticleIn vitro cellular & developmental biology. Animal2019

LncRNA KCNQ1OT1 acting as a ceRNA for miR-4458 enhances osteosarcoma progression by regulating CCND2 expression.

Meng Wang, Zengtao Wang, Xiaolei Zhu, Shibing Guan, Zhibo Liu

Abstract read
PubMed Publisher
In one paragraph

Article in In vitro cellular & developmental biology. Animal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

16 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Osteosarcoma in a ceRNET perspective.Journal of biomedical science · 2024
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. 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.

Meng WangHand and Foot Surgical Center, Provincial Hospital Affiliated to Shandong University, Jinan, 250000, Shangdong, China. wm040390@163.com.
Zengtao WangHand and Foot Surgical Center, Provincial Hospital Affiliated to Shandong University, Jinan, 250000, Shangdong, China.
Xiaolei ZhuHand and Foot Surgical Center, Provincial Hospital Affiliated to Shandong University, Jinan, 250000, Shangdong, China.
Shibing GuanHand and Foot Surgical Center, Provincial Hospital Affiliated to Shandong University, Jinan, 250000, Shangdong, China.
Zhibo LiuHand and Foot Surgical Center, Provincial Hospital Affiliated to Shandong University, Jinan, 250000, Shangdong, China. zhiboLiu_in75@163.com.ORCID http://orcid.org/0000-0001-5582-7193
Shandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteosarcoma is prevalent worldwide and characterized as a challenging health burden. It has been increasingly indicated that long non-coding RNAs (lncRNAs) are significant in pathological processes of numerous cancers, exerting oncogenic or tumor-suppressive function. However, the participation of KCNQ1OT1 in osteosarcoma has not been elaborated. In this study, we focus on interrogating the function of KCNQ1OT1 and its underlying mechanism in osteosarcoma. Our work demonstrated the upregulation of KCNQ1OT1 in osteosarcoma through qRT-PCR. Besides, loss of function assay (CCK-8, transwell migration) indicated KCNQ1OT1 promoted cell proliferation, migration in osteosarcoma. Mechanically, KCNQ1OT1 acting as sponge for miR-4458 antagonized its tumor-suppressive impact on CCND2 expression. The anti-apoptotic nature of KCNQ1OT1 was also unveiled via caspase-3 activity assay. Overexpressed KCNQ1OT1 acted as competing endogenous RNA (ceRNA) for miR-4458 and subsequently reinforced target gene CCND2. Collectively, the results of rescue experiments suggested that the oncogenic role of KCNQ1OT1 was performed through sponging miR-4458 and upregulating CCND2 during osteosarcoma development, providing a novel perspective of intervention in osteosarcoma management.

Indexed as

ApoptosisCarcinogenesisCell Line, TumorCell ProliferationCyclin D2Gene Expression Regulation, NeoplasticHumansMicroRNAsOsteosarcomaRNA, Long NoncodingCCND2 protein, humanCyclin D2KCNQ1OT1 RNAMicroRNAsMIRN-4458 microRNA, humanRNA, Long NoncodingCCND2KCNQ1OT1miR-4458Osteosarcoma

Identifiers

PMID31392505
OpenAlexW2965694825

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.