Evidence map›Paper›PMID 29895198›Full record

ArticleCell cycle (Georgetown, Tex.)2019

Long non-coding RNA GAS5 sensitizes renal cell carcinoma to sorafenib via miR-21/SOX5 pathway.

Lei Liu, Xinlu Pang, Wenjin Shang, Hongchang Xie, Yonghua Feng, Guiwen Feng

RetractedOpen access · bronzeAbstract readRetracted Publication
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

26 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Nucleolar Proteins and Non-Coding RNAs: Roles in Renal Cancer.International journal of molecular sciences · 2021
    Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Lei Liua Department of kidney transplantation , the First Affiliated Hospital of Zhengzhou University , Zhengzhou , Henan Province , P. R. China.
Xinlu Panga Department of kidney transplantation , the First Affiliated Hospital of Zhengzhou University , Zhengzhou , Henan Province , P. R. China.
Wenjin Shanga Department of kidney transplantation , the First Affiliated Hospital of Zhengzhou University , Zhengzhou , Henan Province , P. R. China.
Hongchang Xiea Department of kidney transplantation , the First Affiliated Hospital of Zhengzhou University , Zhengzhou , Henan Province , P. R. China.
Yonghua Fenga Department of kidney transplantation , the First Affiliated Hospital of Zhengzhou University , Zhengzhou , Henan Province , P. R. China.
Guiwen Fenga Department of kidney transplantation , the First Affiliated Hospital of Zhengzhou University , Zhengzhou , Henan Province , P. R. China.
First Affiliated Hospital of Zhengzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although the use of sorafenib appears to increase the survival rate of renal cell carcinoma (RCC) patients, there is also a proportion of patients who exhibit a poor primary response to sorafenib treatment. Therefore, it is critical to elucidate the mechanisms underlying sorafenib resistance and find representative biomarkers for sorafenib treatment in RCC patients. Herein, we identified that a long noncoding RNA GAS5 was downregulated in sorafenib nonresponsive RCCs. GAS5 overexpression conferred sorafenib sensitive to nonresponsive RCC cells, whereas knockdown of GAS5 promoted responsive RCC cells resistant to sorafenib treatment in vitro and in vivo. Mechanistically, GAS5 functioned as competing endogenous RNA to repress miR-21, which controlled its down-stream target SOX5. We proposed that GAS5 was responsible for sorafenib resistance in RCC cells and GAS5 exerted its function through the miR-21/ SOX5 axis. Our findings suggested that GAS5 downregulation may be a new marker of poor response to sorafenib and GAS5 could be a potential therapeutic target for sorafenib treatment in RCC.

Indexed as

AgedAntineoplastic AgentsCarcinoma, Renal CellDrug Resistance, NeoplasmFemaleHumansKidney NeoplasmsMaleMicroRNAsMiddle AgedRNA, Long NoncodingSorafenibSOXD Transcription FactorsAntineoplastic AgentsGAS5 long non-coding RNA, humanMicroRNAsMIRN21 microRNA, humanRNA, Long NoncodingSorafenibSOX5 protein, humanSOXD Transcription FactorsGAS5RCCSorafenib

Identifiers

PMID29895198
PMCPMC6380417
OpenAlexW2808112159

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.