Evidence map›Paper›PMID 16929164›Full record

ArticleCell cycle (Georgetown, Tex.)2006

The problem of cancer dormancy: understanding the basic mechanisms and identifying therapeutic opportunities.

Julio A Aguirre-Ghiso

Open access · greenAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

31 citing papers in PubMed, 61 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. A cancer amidst us: the plexiform lesion in pulmonary arterial hypertension.American journal of physiology. Lung cellular and molecular physiology · 2020
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  9. Review
  10. Crystal structure of truncated human coatomer protein complex subunit ζ1 (Copζ1).Acta crystallographica. Section F, Structural biology communications · 2017
    Article
  11. Article
  12. Article
  13. Article
  14. Modeling boundary conditions for balanced proliferation in metastatic latency.Clinical cancer research : an official journal of the American Association for Cancer Research · 2013
    Article
  15. Impact of deleterious passenger mutations on cancer progression.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
  16. Article
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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

1 author at 1 institution in 1 country.

Julio A Aguirre-GhisoDepartment of Biomedical Sciences, School of Public Health and Center for Excellence in Cancer Genomics, University at Albany, NY, USA. jaguirre-ghiso@albany.edu
University at Albany, State University of New York · 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

The hiatus observed in the progression of cancer after diagnosis and treatment in a large proportion of patients has led to the notion that a state of cancer dormancy must exist during tumor progression. However, research on this stage of cancer has been limited due to the lack of appropriate models and clinical correlates. Fortunately, the last decade has seen the development of new cancer dormancy models, whole animal and intravital imaging techniques and the molecular characterization of minimal residual disease. These studies enabled researchers to reveal intriguing mechanisms and molecular determinants that define tumor dormancy. It is imperative to understand the basic mechanisms of dormancy, as this will accelerate the development of new markers of progression and novel therapeutic opportunities to induce dormancy and/or eradicate dormant disease. This issue of Cell Cycle includes a "Spotlight on Cancer Dormancy" highlighting major contributions to the field of cancer dormancy from basic and clinical studies. We anticipate that this will initiate a forum of discussion on the problem of cancer dormancy and stimulate investigators to study this rather unexplored but undeniably relevant clinical stage of cancer progression.

Indexed as

AnimalsAntineoplastic AgentsApoptosisCell ProliferationCell SurvivalHumansMiceNeoplasm MetastasisNeoplasms, ExperimentalNeoplasm StagingNeoplastic Stem CellsAntineoplastic Agents

Identifiers

PMID16929164
PMCPMC2587296
OpenAlexW2085556725

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.