Evidence map›Paper›PMID 19843243›Full record

ReviewPigment cell & melanoma research2010

Dormancy of metastatic melanoma.

Liliana Ossowski, Julio A Aguirre-Ghiso

Open access · bronzeAbstract readReview
In one paragraph

Review in Pigment cell & melanoma research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
12.3field-weighted citation impact, top 1% 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

58 citing papers in PubMed, 128 citations in OpenAlex.

  1. Article
  2. Review
  3. Dormancy of cutaneous melanoma.Cancer cell international · 2024
    Review
  4. Article
  5. Review
  6. Ferroptosis: A New Road towards Cancer Management.Molecules (Basel, Switzerland) · 2022
    Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. The State of Melanoma: Emergent Challenges and Opportunities.Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
    Article
  13. Review
  14. Article
  15. Pigmentation of conjunctival melanoma recurrences and outcome.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2019
    Article
  16. Two Late Recurrences of Conjunctival Melanoma.Ocular oncology and pathology · 2019
    Article
  17. Article
  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

2 authors at 1 institution in 1 country.

Liliana OssowskiDivision of Hematology and Oncology, Department of Medicine, Mount Sinai School of Medicine, New York, NY, USA. liliana.ossowski@mssm.edu
Julio A Aguirre-Ghiso
Icahn School of Medicine at Mount Sinai · US

Funding

Functional Determinants of Metastatic DormancyR01CA109182 · NCI · STATE UNIVERSITY OF NEW YORK AT ALBANY · PI AGUIRRE-GHISO, JULIO A. · 2005 to 2025
$8.3M
NCI NIH HHS CA109182NCI NIH HHS R01 CA109182
6 · The paper itself

Abstract

Metastatic dormancy of melanoma has not received sufficient attention, most likely because once detectable, metastasis is almost invariably fatal and, understandably, the focus has been on finding ways to prolong life of patients with overt recurrences. Nevertheless, analysis of the published clinical and experimental data on melanoma indicates that some aspect of melanoma biology imitate traits recently associated with dormancy in other solid cancers. Among them the ability of some melanomas to disseminate early during primary tumor progression and once disseminated, to remain undetected (dormant) for years. Comparison of cutaneous and uveal melanoma indicates that, in spite of being of the same origin, they differ profoundly in their clinical progression. Importantly for this discussion, between 40 and 50% of uveal melanoma remain undetected for longer than a decade, while less than 5% of cutaneous melanoma show this behavior. Both types of melanoma have activating oncogene mutations that provide autonomous pro-proliferative signals, yet the consensus is that those are not sufficient for tumor progression. If that is the case, it is possible to envision that signals from outside the tumor cell, (microenvironment) shape the fate of an individual disseminated cell, regardless of an oncogene mutation, to progress or to pause in a state of dormancy. To stimulate further debate and inquiry we describe here a few examples of potential signals that might modify the fate of disseminated cell and provide brief description of the current knowledge on dormancy in other cancers. Our hope is to convince the reader that disseminated melanoma cells do enter periods of prolonged dormancy and that finding ways to induce it, or to prolong it, might mean an extension of symptoms-free life for melanoma patients. Ultimately, understanding the biology of dormancy and the mechanisms of dormant cell survival, might allow for their specific targeting and elimination.

Indexed as

AnimalsCell Transformation, NeoplasticDisease ProgressionEarly Detection of CancerGene Expression Regulation, NeoplasticHumansMelanomaMutationNeoplasm MetastasisNeoplasm Recurrence, LocalSkin NeoplasmsUveal Neoplasms

Identifiers

PMID19843243
PMCPMC2821074
OpenAlexW1500334320

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.