Evidence map›Paper›PMID 25031725›Full record

ArticleInternational journal of clinical and experimental pathology2014

LncRNA TSLC1-AS1 is a novel tumor suppressor in glioma.

Xiaoyong Qin, Jie Yao, Peiliang Geng, Xiangping Fu, Jinghui Xue, Zhiwen Zhang

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
2.1field-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

40 citing papers in PubMed, 1 synthesis or guideline pooled it, 48 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. PTB-AS, a Novel Natural Antisense Transcript, Promotes Glioma Progression by Improving PTBP1 mRNA Stability with SND1.Molecular therapy : the journal of the American Society of Gene Therapy · 2019
    Article
  18. The protean world of non-coding RNAs in glioblastoma.Journal of molecular medicine (Berlin, Germany) · 2019
    Review
  19. Article
  20. Clinical significance of the expression of long non-coding RNA PVT1 in glioma.Cancer biomarkers : section A of Disease markers · 2019
    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 1 institution in 1 country.

Xiaoyong QinDepartment of Neurosurgery, The First Affiliated Hospital of Chinese PLA General Hospital Medical School Beijing 100048, China ; Department of Neurosurgery, 253 Hospital of PLA Huhhot 010051, China.
Jie YaoDepartment of Oncology, 161 Hospital of PLA Jiangan District, Wuhan 430010, Hubei Province, China ; Cancer Center, Chinese PLA General Hospital Medical School Beijing 100853, China.
Peiliang GengCancer Center, Chinese PLA General Hospital Medical School Beijing 100853, China.
Xiangping FuDepartment of Neurosurgery, The First Affiliated Hospital of Chinese PLA General Hospital Medical School Beijing 100048, China.
Jinghui XueDepartment of Neurosurgery, The First Affiliated Hospital of Chinese PLA General Hospital Medical School Beijing 100048, China.
Zhiwen ZhangDepartment of Neurosurgery, The First Affiliated Hospital of Chinese PLA General Hospital Medical School Beijing 100048, China.
Chinese PLA General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Growing evidence demonstrates that long non coding RNAs (lncRNAs) play an important role in cancer origination and progression. A novel lncRNA, TSLC1-AS1, is the antisense transcript of tumor suppressor TSLC1. The expression profile and function of TSLC1-AS1 in glioma were investigated using Real-Time Quantitative PCR and siRNA knockdown. The data showed that TSLC1-AS1 expression was down-regulated in tumor tissues compared with that in adjacent normal tissues, and negatively associated with the WHO criteria of the tumors. Overexpression of TSLC1-AS1 resulted in up-regulation of TSLC1 and significant inhibition of cell proliferation, migration and invasion in U87 cells, while knockdown of TSLC1-AS1 in SNB-19 cells showed the opposite effect. The expression of TSLC1-AS1 was also positively correlated with other tumor suppressors NF1, VHL, PIK3R1 and negatively correlated with the oncogene BRAF. The results suggested that TSLC1-AS1 was a tumor suppressor of glioma and a mediator of TSLC1 expression. LncRNA TSLC1-AS1 may serve as a potential biomarker and therapeutic target for glioma.

Indexed as

Cell Adhesion Molecule-1Cell Adhesion MoleculesCell Line, TumorGene Expression Regulation, NeoplasticGenes, Tumor SuppressorGliomaHumansImmunoglobulinsReal-Time Polymerase Chain ReactionRNA, Long NoncodingRNA, Small InterferingTranscriptomeTransfectionCADM1 protein, humanCell Adhesion Molecule-1Cell Adhesion MoleculesImmunoglobulinsRNA, Long NoncodingRNA, Small InterferinggliomaLong non coding RNAstumor suppressor

Identifiers

PMID25031725
PMCPMC4097230
OpenAlexW1748472291

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.