Evidence map›Paper›PMID 27530352›Full record

ArticleOncogene2017

The long non-coding RNA, SNHG6-003, functions as a competing endogenous RNA to promote the progression of hepatocellular carcinoma.

C Cao, T Zhang, D Zhang, L Xie, X Zou, L Lei, D Wu, L Liu

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 106 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
106citing papers in PubMed, 3 pooled it
10.6field-weighted citation impact, top 1% 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

106 citing papers in PubMed, 3 syntheses or guidelines pooled it, 190 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. HCC-Related lncRNAs: Roles and Mechanisms.International journal of molecular sciences · 2024
    Review
  11. Review
  12. Article
  13. Article
  14. LncRNA SNHG6 role in clinicopathological parameters in cancers.European journal of medical research · 2023
    Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article

46 more citing papers are in PubMed but not listed here.

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

8 authors at 3 institutions in 2 countries.

C CaoDepartment of Radiation Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
T ZhangGuangdong Provincial Key Laboratory of Viral Hepatitis Research, Guangzhou, China.
D ZhangDepartment of Radiation Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
L XieCenter for Molecular Medicine, University of Georgia, Athens, GA, USA.
X ZouGuangdong Provincial Key Laboratory of Viral Hepatitis Research, Guangzhou, China.
L LeiDepartment of Radiation Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
D WuDepartment of Radiation Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
L LiuGuangdong Provincial Key Laboratory of Viral Hepatitis Research, Guangzhou, China.
Southern Medical University · CNKey Laboratory of Guangdong Province · CNUniversity of Georgia · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The expression of long non-coding RNAs (lncRNAs) is dysregulated in hepatocellular carcinoma (HCC). However, the functions and contributions of lncRNAs remain largely unknown. Here, we identified a critical role of SNHG6-003 in HCC. We found that five SNHG6 transcripts were differentially expressed in HCC tissues while only the SNHG6-003 had an oncogenic function. Ectopic expression of SNHG6-003 in HCC cells promoted cell proliferation and induced drug resistance, whereas SNHG6-003 knockdown promoted apoptosis. Moreover, SNHG6-003 functioned as a competitive endogenous RNA (ceRNA), effectively becoming sponge for miR-26a/b and thereby modulating the expression of transforming growth factor-β-activated kinase 1 (TAK1). Importantly, expression analysis revealed that both SNHG6-003 and TAK1 were upregulated in human cancers, exhibiting a co-expression pattern. In HCC patients, high expression of SNHG6-003 closely correlated with tumor progression and shorter survival. Thus, targeting the ceRNA network involving SNHG6-003 may be used as a treatment strategy against HCC.

Indexed as

Gene Expression Regulation, NeoplasticBiomarkers, TumorCarcinoma, HepatocellularDisease ProgressionHumansLiver NeoplasmsMAP Kinase Kinase Kinase 7MAP Kinase Kinase KinasesMicroRNAsNeoplasm StagingPrognosisRNA, Long NoncodingRNA, NeoplasmSignal TransductionTumor Cells, CulturedBiomarkers, TumorMAP Kinase Kinase Kinase 7MAP Kinase Kinase KinasesMicroRNAsMIRN26 microRNA, humanRNA, Long NoncodingRNA, Neoplasm

Identifiers

PMID27530352
OpenAlexW2512011967

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.