Evidence map›Paper›PMID 29369542›Full record

ArticleJournal of cellular and molecular medicine2018

Identification of Sox6 as a regulator of pancreatic cancer development.

Weiliang Jiang, Qiongying Yuan, Yuanye Jiang, Li Huang, Congying Chen, Guoyong Hu, Rong Wan, Xingpeng Wang, Lijuan Yang

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.9field-weighted citation impact, top 11% 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

25 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. SOX on tumors, a comfort or a constraint?Cell death discovery · 2024
    Review
  6. Article
  7. Article
  8. Article
  9. Corrigendum.Journal of cellular and molecular medicine · 2022
    Article
  10. NMilitary Medical Research · 2022
    Article
  11. Article
  12. Review
  13. Article
  14. Inhibition of lncRNA MAAT Controls Multiple Types of Muscle Atrophy by cis- and trans-Regulatory Actions.Molecular therapy : the journal of the American Society of Gene Therapy · 2021
    Article
  15. Observational
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Weiliang JiangDepartment of Gastroenterology, School of Medicine, Shanghai General Hospital/First People's Hospital, Shanghai Jiao Tong University, Shanghai, China.
Qiongying YuanDepartment of Gastroenterology, School of Medicine, Shanghai East Hospital, Tongji University, Shanghai, China.
Yuanye JiangDepartment of Gastroenterology, The Central Hospital of Putuo District, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Li HuangDepartment of Gastroenterology, School of Medicine, Shanghai General Hospital/First People's Hospital, Shanghai Jiao Tong University, Shanghai, China.
Congying ChenDepartment of Gastroenterology, School of Medicine, Shanghai General Hospital/First People's Hospital, Shanghai Jiao Tong University, Shanghai, China.
Guoyong HuDepartment of Gastroenterology, School of Medicine, Shanghai General Hospital/First People's Hospital, Shanghai Jiao Tong University, Shanghai, China.
Rong WanDepartment of Gastroenterology, School of Medicine, Shanghai General Hospital/First People's Hospital, Shanghai Jiao Tong University, Shanghai, China.
Xingpeng WangDepartment of Gastroenterology, School of Medicine, Shanghai General Hospital/First People's Hospital, Shanghai Jiao Tong University, Shanghai, China.
Lijuan YangDepartment of Gastroenterology, School of Medicine, Shanghai General Hospital/First People's Hospital, Shanghai Jiao Tong University, Shanghai, China.ORCID 0000-0002-0521-7810
Shanghai Jiao Tong University · CNShanghai East Hospital · CNShanghai University of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pancreatic cancer (PC) is an aggressive malignancy associated with a poor prognosis and low responsiveness to chemotherapy and radiotherapy. Most patients with PC have metastatic disease at diagnosis, which partly accounts for the high mortality from this disease. Here, we explored the role of the transcription factor sex-determining region Y-box (Sox) 6 in the invasiveness of PC cells. We showed that Sox6 is down-regulated in patients with PC in association with metastatic disease. Sox6 overexpression suppressed PC cell proliferation and migration in vitro and tumour growth and liver metastasis in vivo. Sox6 inhibited epithelial-mesenchymal transition (EMT), and Akt signalling. Sox6 was shown to interact with the promoter of Twist1, a helix-loop-helix transcription factor involved in the induction of EMT, and to modulate the expression of Twist1 by recruiting histone deacetylase 1 to the promoter of the Twist1 gene. Twist1 overexpression reversed the effect of Sox6 on inhibiting EMT, confirming that the effect of Sox6 on suppressing tumour invasiveness is mediated by the modulation of Twist1 expression. These results suggest a novel mechanism underlying the aggressive behaviour of PC cells and identify potential therapeutic targets for the treatment of PC.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsCarcinogenesisCell Line, TumorCell MovementCell ProliferationEpithelial-Mesenchymal TransitionHistone Deacetylase 1HumansLiver NeoplasmsMaleMiceMice, Inbred BALB CMice, NudeNeoplasm InvasivenessNuclear ProteinsHDAC1 protein, humanHistone Deacetylase 1Nuclear ProteinsProto-Oncogene Proteins c-aktRNA, Small InterferingSOX6 protein, humanSOXD Transcription FactorsTWIST1 protein, humanTwist-Related Protein 1epithelial-mesenchymal transitionpancreatic cancerSox6Twist1

Identifiers

PMID29369542
PMCPMC5824410
OpenAlexW2791178241

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.