Evidence map›Paper›PMID 31781319›Full record

ArticleOxidative medicine and cellular longevity2019

Enhanced p62-NRF2 Feedback Loop due to Impaired Autophagic Flux Contributes to Arsenic-Induced Malignant Transformation of Human Keratinocytes.

Xiafang Wu, Ru Sun, Huihui Wang, Bei Yang, Fang Wang, Hongtao Xu, Shimin Chen, Rui Zhao, Jingbo Pi, Yuanyuan Xu

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

15 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. The intricacies of NRF2 regulation in cancer.Seminars in cancer biology · 2021
    Review
  11. Article
  12. The Role of Toxic Metals and Metalloids in Nrf2 Signaling.Antioxidants (Basel, Switzerland) · 2021
    Review
  13. Article
  14. The Interaction of lncRNA XLOC-2222497,International journal of molecular sciences · 2020
    Article
  15. Review
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

10 authors at 2 institutions in 1 country.

Xiafang WuSchool of Public Health, China Medical University, China.
Ru SunSchool of Public Health, China Medical University, China.
Huihui WangSchool of Public Health, China Medical University, China.
Bei YangCollege of Basic Medical Sciences, China Medical University, China.
Fang WangSchool of Public Health, China Medical University, China.
Hongtao XuCollege of Basic Medical Sciences, China Medical University, China.
Shimin ChenSchool of Public Health, China Medical University, China.
Rui ZhaoSchool of Forensic Medicine, China Medical University, China.
Jingbo PiSchool of Public Health, China Medical University, China.ORCID https://orcid.org/0000-0003-0227-8041
Yuanyuan XuSchool of Public Health, China Medical University, China.ORCID https://orcid.org/0000-0003-2354-9453
China Medical University · CNFirst Hospital of China Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic exposure to arsenic induces a variety of cancers, particularly in the skin. Autophagy is a highly conserved process which plays a dual role in tumorigenesis. In the present study, we found that chronic exposure to an environmentally relevant dose of arsenite induced malignant transformation of human keratinocytes (HaCaT) with dysregulated autophagy as indicated by an increased number of autophagosomes, activation of mTORC1 pathway, and elevated protein levels of p62 and LC3II. Meanwhile, arsenite-transformed cells showed lower intracellular levels of reactive oxygen species compared with control. Silencing

Indexed as

ArsenicAutophagic Cell DeathCell LineCell Transformation, NeoplasticFeedback, PhysiologicalHumansKeratinocytesMechanistic Target of Rapamycin Complex 1Neoplasm ProteinsNF-E2-Related Factor 2ProteolysisRNA-Binding ProteinsRNA, NeoplasmSignal TransductionArsenicMechanistic Target of Rapamycin Complex 1Neoplasm ProteinsNFE2L2 protein, humanNF-E2-Related Factor 2P62 protein, humanRNA-Binding ProteinsRNA, Neoplasm

Identifiers

PMID31781319
PMCPMC6875345
OpenAlexW2982631521

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.