Evidence map›Paper›PMID 34458153›Full record

ArticleFrontiers in oncology2021

ATG5 and ATG7 Expression Levels Are Reduced in Cutaneous Melanoma and Regulated by NRF1.

Živa Frangež, Deborah Gérard, Zhaoyue He, Marios Gavriil, Yuniel Fernández-Marrero, S Morteza Seyed Jafari, Robert E Hunger, Philippe Lucarelli, Shida Yousefi, Thomas Sauter and 2 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2021. 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 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
4.1field-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

24 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Autophagy · 2026
    Article
  5. Article
  6. Multimodal HSI-MRI system for tumor delineation in neurosurgical guidance.International journal of computer assisted radiology and surgery · 2026
    Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Bioinformatics analysis identifiesTranslational cancer research · 2025
    Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Review
  17. Review
  18. Article
  19. Autophagy and autophagy-related pathways in cancer.Nature reviews. Molecular cell biology · 2023
    Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 2 institutions in 5 countries.

Živa FrangežInstitute of Pharmacology, University of Bern, Bern, Switzerland.
Deborah GérardDepartment of Life Sciences and Medicine, University of Luxembourg, Belvaux, Luxembourg.
Zhaoyue HeInstitute of Pharmacology, University of Bern, Bern, Switzerland.
Marios GavriilDepartment of Life Sciences and Medicine, University of Luxembourg, Belvaux, Luxembourg.
Yuniel Fernández-MarreroInstitute of Pharmacology, University of Bern, Bern, Switzerland.
S Morteza Seyed JafariDepartment of Dermatology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Robert E HungerDepartment of Dermatology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Philippe LucarelliDepartment of Life Sciences and Medicine, University of Luxembourg, Belvaux, Luxembourg.
Shida YousefiInstitute of Pharmacology, University of Bern, Bern, Switzerland.
Thomas SauterDepartment of Life Sciences and Medicine, University of Luxembourg, Belvaux, Luxembourg.
Lasse SinkkonenDepartment of Life Sciences and Medicine, University of Luxembourg, Belvaux, Luxembourg.
Hans-Uwe SimonInstitute of Pharmacology, University of Bern, Bern, Switzerland.
University of Bern · CHUniversity of Luxembourg · LU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autophagy is a highly conserved cellular process in which intracellular proteins and organelles are sequestered and degraded after the fusion of double-membrane vesicles known as autophagosomes with lysosomes. The process of autophagy is dependent on autophagy-related (ATG) proteins. The role of autophagy in cancer is very complex and still elusive. We investigated the expression of ATG proteins in benign nevi, primary and metastatic melanoma tissues using customized tissue microarrays (TMA). Results from immunohistochemistry show that the expression of ATG5 and ATG7 is significantly reduced in melanoma tissues compared to benign nevi. This reduction correlated with changes in the expression of autophagic activity markers, suggesting decreased basal levels of autophagy in primary and metastatic melanomas. Furthermore, the analysis of survival data of melanoma patients revealed an association between reduced ATG5 and ATG7 levels with an unfavourable clinical outcome. Currently, the mechanisms regulating ATG expression levels in human melanoma remains unknown. Using bioinformatic predictions of transcription factor (TF) binding motifs in accessible chromatin of primary melanocytes, we identified new TFs involved in the regulation of core ATGs. We then show that nuclear respiratory factor 1 (NRF1) stimulates the production of mRNA and protein as well as the promoter activity of

Indexed as

ATG5ATG7autophagymelanomaNRF1transcription factor

Identifiers

PMID34458153
PMCPMC8397460
OpenAlexW3187423241

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.