Evidence map›Paper›PMID 25118602›Full record

ReviewNature reviews. Cancer2014

Mechanisms of disseminated cancer cell dormancy: an awakening field.

María Soledad Sosa, Paloma Bragado, Julio A Aguirre-Ghiso

Abstract readReview
In one paragraph

Review in Nature reviews. Cancer, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 713 papers.

0numbers the graph read from it
0cells of the map it votes in
713citing papers in PubMed
–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

713 citing papers in PubMed.

  1. Trial
  2. Niches in cancer: from primary tumors to metastatic disease.Journal of hematology & oncology · 2026
    Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Review
  16. Review
  17. Article
  18. Review
  19. Rewiring dormancy.Nature cell biology · 2026
    Article
  20. Review

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

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

3 authors.

María Soledad Sosa1] Division of Hematology and Oncology, Department of Medicine, Department of Otolaryngology, Tisch Cancer Institute, New York NY 10029, USA. [2] Black Family Stem Cell Institute, Ichan School of Medicine at Mount Sinai, New York NY 10029, USA. [3].
Paloma Bragado1] Division of Hematology and Oncology, Department of Medicine, Department of Otolaryngology, Tisch Cancer Institute, New York NY 10029, USA. [2] Black Family Stem Cell Institute, Ichan School of Medicine at Mount Sinai, New York NY 10029, USA. [3] Molecular and Translational Oncology Laboratory, Institut d'Investigacions Biomèdiques August Pi I Sunyer, Barcelona 08036, Spain. [4].
Julio A Aguirre-Ghiso1] Division of Hematology and Oncology, Department of Medicine, Department of Otolaryngology, Tisch Cancer Institute, New York NY 10029, USA. [2] Black Family Stem Cell Institute, Ichan School of Medicine at Mount Sinai, New York NY 10029, USA.

Funding

Functional Determinants of Metastatic DormancyR01CA109182 · NCI · STATE UNIVERSITY OF NEW YORK AT ALBANY · PI AGUIRRE-GHISO, JULIO A. · 2005 to 2025
$8.3M
Tumor microenvironments determing migration, dissemination and dormancyU54CA163131 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI AGUIRRE-GHISO, JULIO A., CASTRACANE, JAMES · 2011 to 2015
$3.9M
NCI NIH HHS CA109182NCI NIH HHS CA163131NCI NIH HHS R01 CA109182NCI NIH HHS U54 CA163131
6 · The paper itself

Abstract

Metastases arise from residual disseminated tumour cells (DTCs). This can happen years after primary tumour treatment because residual tumour cells can enter dormancy and evade therapies. As the biology of minimal residual disease seems to diverge from that of proliferative lesions, understanding the underpinnings of this new cancer biology is key to prevent metastasis. Analysis of approximately 7 years of literature reveals a growing focus on tumour and normal stem cell quiescence, extracellular and stromal microenvironments, autophagy and epigenetics as mechanisms that dictate tumour cell dormancy. In this Review, we attempt to integrate this information and highlight both the weaknesses and the strengths in the field to provide a framework to understand and target this crucial step in cancer progression.

Indexed as

AutophagyEpigenesis, GeneticHumansNeoplasm, ResidualNeoplasmsNeovascularization, PathologicSignal TransductionStress, PhysiologicalTumor Microenvironment

Identifiers

PMID25118602
PMCPMC4230700

What OpenQuestion holds

Textmetadata
LicenceTDM
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.