Evidence map›Paper›PMID 31933968›Full record

ArticleInternational journal of clinical and experimental pathology2019

Knockdown of lncRNA XIST suppresses osteosarcoma progression by inactivating AKT/mTOR signaling pathway by sponging miR-375-3p.

Xin Sun, Bo Wei, Zhi-Heng Peng, Qing-Long Fu, Chao-Jun Wang, Jin-Chang Zheng, Jie-Cong Sun

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

22 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Potential roles of lncRNA-XIST/miRNAs/mRNAs in human cancer cells.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Expression of long noncoding RNAFrontiers in endocrinology · 2022
    Article
  12. Long non-coding RNA XIST: a novel oncogene in multiple cancers.Molecular medicine (Cambridge, Mass.) · 2021
    Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Biological Function of Long Non-coding RNA (LncRNA) Xist.Frontiers in cell and developmental biology · 2021
    Review
  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

7 authors at 1 institution in 1 country.

Xin SunOrthopaedic Center, Affiliated Hospital of Guangdong Medical University Xiashan District, Zhanjiang, Guangdong Province, China.
Bo WeiOrthopaedic Center, Affiliated Hospital of Guangdong Medical University Xiashan District, Zhanjiang, Guangdong Province, China.
Zhi-Heng PengOrthopaedic Center, Affiliated Hospital of Guangdong Medical University Xiashan District, Zhanjiang, Guangdong Province, China.
Qing-Long FuOrthopaedic Center, Affiliated Hospital of Guangdong Medical University Xiashan District, Zhanjiang, Guangdong Province, China.
Chao-Jun WangOrthopaedic Center, Affiliated Hospital of Guangdong Medical University Xiashan District, Zhanjiang, Guangdong Province, China.
Jin-Chang ZhengOrthopaedic Center, Affiliated Hospital of Guangdong Medical University Xiashan District, Zhanjiang, Guangdong Province, China.
Jie-Cong SunOrthopaedic Center, Affiliated Hospital of Guangdong Medical University Xiashan District, Zhanjiang, Guangdong Province, China.
Guangdong Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOsteosarcoma (OS) is one of the most common bone tumors in adolescents and young adults. Emerging evidence suggested ncRNA (lncRNA and miRNA) are closely associated with cell progression, apoptosis and autophagy. However, the role of regulatory network between ncRNA and mRNA in OS has not been fully verified.

methodslncRNA XIST, miRNA expression were detected by qRT-PCR. The protein expression of LC3, p62, AKT, p-AKT, mTOR and p-mTOR was measured by western blot. MTT assay and flow cytometry were applied to measure cell proliferation and apoptosis. Luciferase assay was used to ensure the relationship between lncRNA, miRNA and mRNA. GFP-LC3 cells were observed using fluorescence microscope.

resultsXIST expression was up-regulated but miR-375-3p was down-regulated in OS tissues and cells. Luciferase assay results demonstrated that miR-375-3p was a target of XIST and mTOR was a target mRNA of miR-375-3p. In addition, knockdown of XIST and mTOR inhibited OS cell proliferation and autophagy, but induced apoptosis. Knockdown of XIST could reverse the effect of miR-375-3p inhibitor on OS cells. The effects of si-mTOR of OS cells could be reversed by silencing miR-375-3p. Moreover, knockdown of XIST inhibited AKT/mTOR signaling pathway via sponging miR-375-3p.

conclusionKnockdown of XIST inhibited cell growth and autophagy but induced cell apoptosis by suppressing the AKT/mTOR signaling pathway by sponging miR-375-3p.

Indexed as

AKT/mTORmiR-375-3pOsteosarcomaXIST

Identifiers

PMID31933968
PMCPMC6947095
OpenAlexW3009989377

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.