Evidence map›Paper›PMID 17510285›Full record

ArticleGenes & development2007

Autophagy suppresses tumor progression by limiting chromosomal instability.

Robin Mathew, Sameera Kongara, Brian Beaudoin, Cristina M Karp, Kevin Bray, Kurt Degenhardt, Guanghua Chen, Shengkan Jin, Eileen White

Erratum issuedOpen access · diamondAbstract read
In one paragraph

Article in Genes & development, 2007. 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 523 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
523citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

523 citing papers in PubMed, 1 synthesis or guideline pooled it, 918 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Article
  5. Autophagy modulation in cancer.Nature reviews. Drug discovery · 2026
    Review
  6. Autophagy in Melanoma: Molecular Mechanisms and Therapeutic Perspectives.International journal of molecular sciences · 2026
    Review
  7. MinimalRSC chemical biology · 2026
    Article
  8. Review
  9. Review
  10. Review
  11. Autophagy in Ovarian Cancer, an Opportunity or an Additional Threat?International journal of molecular sciences · 2026
    Review
  12. Article
  13. A CHKA-PML autophagy checkpoint enables tumors to evade glutamine starvation.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  14. Article
  15. Article
  16. Article
  17. Dual regulation of autophagy: paradoxical effects on tumor angiogenesis.Frontiers in cell and developmental biology · 2026
    Review
  18. Review
  19. Article
  20. Review

463 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Robin MathewUniversity of Medicine and Dentistry of New Jersey, Robert Wood Johnson Medical School, Piscataway, New Jersey 08854, USA.
Sameera Kongara
Brian Beaudoin
Cristina M Karp
Kevin Bray
Kurt Degenhardt
Guanghua Chen
Shengkan Jin
Eileen White
Rutgers, The State University of New Jersey · USCancer Institute of Florida · USRutgers Cancer Institute of New Jersey

Funding

Function of the Adenovirus E1B OncogeneR37CA053370 · NCI · RUTGERS THE ST UNIV OF NJ NEW BRUNSWICK · PI WHITE, EILEEN P. · 2001 to 2009
$3.1M
NCI NIH HHS R37 CA053370NCI NIH HHS R37 CA53370
6 · The paper itself

Abstract

Autophagy is a bulk degradation process that promotes survival under metabolic stress, but it can also be a means of cell death if executed to completion. Monoallelic loss of the essential autophagy gene beclin1 causes susceptibility to metabolic stress, but also promotes tumorigenesis. This raises the paradox that the loss of a survival pathway enhances tumor growth, where the exact mechanism is not known. Here, we show that compromised autophagy promoted chromosome instability. Failure to sustain metabolism through autophagy was associated with increased DNA damage, gene amplification, and aneuploidy, and this genomic instability may promote tumorigenesis. Thus, autophagy maintains metabolism and survival during metabolic stress that serves to protect the genome, providing an explanation for how the loss of a survival pathway leads to tumor progression. Identification of this novel role of autophagy may be important for rational chemotherapy and therapeutic exploitation of autophagy inducers as potential chemopreventive agents.

Indexed as

Chromosomal InstabilityAnimalsApoptosisApoptosis Regulatory ProteinsAspartic AcidAutophagyAutophagy-Related Protein 5Beclin-1Blotting, WesternCells, CulturedCentrosomeChromosome AberrationsDisease ProgressionDNA DamageEpithelial CellsFluorescent Antibody TechniqueApoptosis Regulatory ProteinsAspartic AcidAtg5 protein, mouseAutophagy-Related Protein 5Beclin-1Becn1 protein, mouseMicrotubule-Associated ProteinsPhosphonoacetic AcidProteinsProto-Oncogene Proteins c-bcl-2pyrimidinePyrimidinessparfosic acid

Identifiers

PMID17510285
PMCPMC1877749
OpenAlexW2163147674

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.