Evidence map›Paper›PMID 32142731›Full record

ArticleThe American journal of pathology2020

Oxidative Phosphorylation Promotes Primary Melanoma Invasion.

Amel Salhi, Alexander C Jordan, Irineu I Bochaca, Allison Izsak, Farbod Darvishian, Yariv Houvras, Keith M Giles, Iman Osman

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2020. 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 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.6field-weighted citation impact, top 17% 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, 32 citations in OpenAlex.

  1. Article
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  4. Article
  5. Review
  6. Review
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  8. Article
  9. Article
  10. Metabolic insights into tumor lymph node metastasis in melanoma.Cellular oncology (Dordrecht, Netherlands) · 2024
    Review
  11. Article
  12. A metabolic perspective on nitric oxide function in melanoma.Biochimica et biophysica acta. Reviews on cancer · 2024
    Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Connecting Metabolic Rewiring With Phenotype Switching in Melanoma.Frontiers in cell and developmental biology · 2022
    Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Amel SalhiRonald O. Perelman Department of Dermatology, New York University School of Medicine, New York, New York.
Alexander C JordanRonald O. Perelman Department of Dermatology, New York University School of Medicine, New York, New York.
Irineu I BochacaRonald O. Perelman Department of Dermatology, New York University School of Medicine, New York, New York.
Allison IzsakRonald O. Perelman Department of Dermatology, New York University School of Medicine, New York, New York.
Farbod DarvishianDepartment of Pathology, New York University School of Medicine, New York, New York.
Yariv HouvrasDepartment of Surgery, Weill Cornell Medical College, New York, New York.
Keith M GilesRonald O. Perelman Department of Dermatology, New York University School of Medicine, New York, New York. Electronic address: keith.giles@nyumc.org.
Iman OsmanRonald O. Perelman Department of Dermatology, New York University School of Medicine, New York, New York. Electronic address: iman.osman@nyumc.org.
New York University · USCornell University · US

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ADRIANA HEGUY · 1985 to 2026
$83.1M
Project 4P50CA225450 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI OSMAN, IMAN, WEBER, JEFFREY S · 2019 to 2025
$12.5M
NCI NIH HHS P30 CA016087NCI NIH HHS P50 CA225450
6 · The paper itself

Abstract

Dermal invasion is a hallmark of malignant melanoma. Although the molecular alterations that drive the progression of primary melanoma to metastatic disease have been studied extensively, the early progression of noninvasive primary melanoma to an invasive state is poorly understood. To elucidate the mechanisms underlying the transition from radial to vertical growth, the first step in melanoma invasion, we developed a zebrafish melanoma model in which constitutive activation of ribosomal protein S6 kinase A1 drives tumor invasion. Transcriptomic analysis of ribosomal protein S6 kinase A1-activated tumors identified metabolic changes, including up-regulation of genes associated with oxidative phosphorylation. Vertical growth phase human melanoma cells show higher oxygen consumption and preferential utilization of glutamine compared to radial growth phase melanoma cells. Peroxisome proliferator activated receptor γ coactivator (PGC)-1α, has been proposed as a master regulator of tumor oxidative phosphorylation. In human primary melanoma specimens, PGC1α protein expression was found to be positively associated with increased tumor thickness and expression of the proliferative marker Ki-67 and the reactive oxygen species scavenger receptor class A member 3. PGC1α depletion modulated cellular processes associated with primary melanoma growth and invasion, including oxidative stress. These results support a role for PGC1α in mediating glutamine-driven oxidative phosphorylation to facilitate the invasive growth of primary melanoma.

Indexed as

Oxidative PhosphorylationAnimalsHeterograftsHumansMelanomaNeoplasm InvasivenessPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaZebrafishPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPPARGC1A protein, human

Identifiers

PMID32142731
PMCPMC7237828
OpenAlexW3010215117

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.