Evidence map›Paper›PMID 27308509›Full record

ArticleMolecular & cellular oncology

HIGD1A-mediated dormancy and tumor survival.

Kurosh Ameri, Emin Maltepe

Open access · hybridAbstract read
In one paragraph

Article in Molecular & cellular oncology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.5field-weighted citation impact, top 36% 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

12 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Cellular senescence or stemness: hypoxia flips the coin.Journal of experimental & clinical cancer research : CR · 2021
    Review
  9. Article
  10. Higd1a Protects Cells from Lipotoxicity under High-Fat Exposure.Oxidative medicine and cellular longevity · 2019
    Article
  11. Review
  12. 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

2 authors at 1 institution in 1 country.

Kurosh AmeriDepartment of Pediatrics; University of California, San Francisco ; San Francisco, CA, USA.
Emin MaltepeDepartment of Pediatrics; University of California, San Francisco; San Francisco, CA, USA; Department of Biomedical Sciences; University of California, San Francisco; San Francisco, CA, USA; Department of Developmental and Stem Cell Biology; University of California, San Francisco; San Francisco, CA, USA.
University of California, San Francisco · US

Funding

Integrating Environmental Cues at the Maternal-Fetal Vascular InterfaceR01HD072455 · NICHD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MALTEPE, EMIN · 2012 to 2023
$4.3M
NICHD NIH HHS R01 HD072455
6 · The paper itself

Abstract

Solid tumors contain regions of anoxia that are also glucose deprived. How cancer cells survive such extreme conditions remains unclear. Here, we discuss our recent findings that regulation of hypoxia inducible gene domain family member 1 A (HIGD1A) via epigenetic mechanisms during glucose starvation modulates oxygen consumption and reactive oxygen species production to enable tumor cell survival through the activation of dormancy mechanisms.

Indexed as

AMPKDNMT1glucose deprivationHIFhypoxiatumor dormancy

Identifiers

PMID27308509
PMCPMC4905353
OpenAlexW1574703626

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.