Evidence map›Paper›PMID 25683712›Full record

ArticleCell reports2015

HIGD1A Regulates Oxygen Consumption, ROS Production, and AMPK Activity during Glucose Deprivation to Modulate Cell Survival and Tumor Growth.

Kurosh Ameri, Arman Jahangiri, Anthony M Rajah, Kathryn V Tormos, Ravi Nagarajan, Melike Pekmezci, Vien Nguyen, Matthew L Wheeler, Michael P Murphy, Timothy A Sanders and 6 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

59 citing papers in PubMed, 103 citations in OpenAlex.

  1. Article
  2. Review
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  4. Article
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  6. Article
  7. Article
  8. mCell death and differentiation · 2024
    Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Structure and function of theProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  15. Mitochondrial Factors in the Cell Nucleus.International journal of molecular sciences · 2023
    Review
  16. Review
  17. Review
  18. Article
  19. Article
  20. Article
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

16 authors at 4 institutions in 2 countries.

Kurosh AmeriDepartment of Pediatrics/Biomedical Sciences, University of California San Francisco, San Francisco, CA 94143, USA.
Arman JahangiriDepartment of Neurological Surgery, University of California San Francisco, San Francisco, CA 94143, USA.
Anthony M RajahDepartment of Pediatrics/Biomedical Sciences, University of California San Francisco, San Francisco, CA 94143, USA.
Kathryn V TormosDepartment of Pediatrics/Biomedical Sciences, University of California San Francisco, San Francisco, CA 94143, USA.
Ravi NagarajanDepartment of Neurological Surgery, University of California San Francisco, San Francisco, CA 94143, USA.
Melike PekmezciDepartment of Pathology, University of California San Francisco, San Francisco, CA 94143, USA.
Vien NguyenDepartment of Biomedical Sciences, University of California San Francisco, San Francisco, CA 94143, USA.
Matthew L WheelerDepartment of Microbiology/Immunology, University of California San Francisco, San Francisco, CA 94143, USA.
Michael P MurphyMitochondrial Biology Unit, MRC, Cambridge CB2 0XY, UK.
Timothy A SandersDepartment of Pediatrics/Biomedical Sciences, University of California San Francisco, San Francisco, CA 94143, USA.
Stefanie S JeffreyDepartment of Surgery, Stanford University School of Medicine, Stanford, CA 94305, USA.
Yerem YeghiazariansDepartment of Medicine/CVRI/Eli and Edythe Broad Center for Regeneration Medicine, University of California San Francisco, San Francisco, CA 94143, USA.
Paolo F RinaudoDepartment of Obstetrics, Gynecology/Reproductive Sciences, University of California San Francisco, San Francisco, CA 94143, USA.
Joseph F CostelloDepartment of Neurological Surgery, University of California San Francisco, San Francisco, CA 94143, USA.
Manish K AghiDepartment of Neurological Surgery, University of California San Francisco, San Francisco, CA 94143, USA.
Emin MaltepeDepartment of Pediatrics/Biomedical Sciences, University of California San Francisco, San Francisco, CA 94143, USA. Electronic address: emin.maltepe@ucsf.edu.
Neurological Surgery · USUniversity of California, San Francisco · USMRC Mitochondrial Biology Unit · GBStanford University · US

Funding

Project 4: Multi-modality Metabolic Imaging for Monitoring Molecular Sub-types of GliomaP01CA118816 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Susan M Chang, Janine Marie Lupo · 2007 to 2026
$44.7M
Integrating Environmental Cues at the Maternal-Fetal Vascular InterfaceR01HD072455 · NICHD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MALTEPE, EMIN · 2012 to 2023
$4.3M
Tumor cell and microenvironment changes causing antiangiogenic therapy resistanceR01NS079697 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI AGHI, MANISH · 2013 to 2021
$3.2M
Medical Research Council MC_U105663142NCI NIH HHS P01 CA118816NICHD NIH HHS R01 HD072455NINDS NIH HHS R01 NS079697
6 · The paper itself

Abstract

Hypoxia-inducible gene domain family member 1A (HIGD1A) is a survival factor induced by hypoxia-inducible factor 1 (HIF-1). HIF-1 regulates many responses to oxygen deprivation, but viable cells within hypoxic perinecrotic solid tumor regions frequently lack HIF-1α. HIGD1A is induced in these HIF-deficient extreme environments and interacts with the mitochondrial electron transport chain to repress oxygen consumption, enhance AMPK activity, and lower cellular ROS levels. Importantly, HIGD1A decreases tumor growth but promotes tumor cell survival in vivo. The human Higd1a gene is located on chromosome 3p22.1, where many tumor suppressor genes reside. Consistent with this, the Higd1a gene promoter is differentially methylated in human cancers, preventing its hypoxic induction. However, when hypoxic tumor cells are confronted with glucose deprivation, DNA methyltransferase activity is inhibited, enabling HIGD1A expression, metabolic adaptation, and possible dormancy induction. Our findings therefore reveal important new roles for this family of mitochondrial proteins in cancer biology.

Identifiers

PMID25683712
PMCPMC4534363
OpenAlexW2031958947

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.