Evidence map›Paper›PMID 33979673›Full record

ReviewSeminars in cancer biology2022

Thorny ground, rocky soil: Tissue-specific mechanisms of tumor dormancy and relapse.

Andrea R Lim, Cyrus M Ghajar

Open access · greenAbstract readReview
In one paragraph

Review in Seminars in cancer biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.3field-weighted citation impact, top 9% 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

27 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
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  14. Article
  15. Targeting cancer cell dormancy.Nature reviews. Cancer · 2024
    Article
  16. Review
  17. Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  18. Dormancy in Breast Cancer.Cold Spring Harbor perspectives in medicine · 2023
    Review
  19. Organ-Specificity of Breast Cancer Metastasis.International journal of molecular sciences · 2023
    Review
  20. Review
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.

Andrea R LimPublic Health Sciences Division/Translational Research Program, Fred Hutchinson Cancer Research Center, Seattle, WA, USA; Graduate Program in Molecular and Cellular Biology, University of Washington/Fred Hutchinson Cancer Research Center, Seattle, WA, USA; Human Biology Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA. Electronic address: arlim@fredhutch.org.
Cyrus M GhajarPublic Health Sciences Division/Translational Research Program, Fred Hutchinson Cancer Research Center, Seattle, WA, USA; Human Biology Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA. Electronic address: cghajar@fredhutch.org.
Fred Hutch Cancer Center · US

Funding

Project 3: Single Cell Measures of Intratumor Diversity for Optimal Breast Cancer TherapyU54CA193461 · NCI · DANA-FARBER CANCER INST · PI POLYAK, KORNELIA · 2015 to 2020
$11.2M
Defining and characterizing microenvironmental drivers of disseminated tumor cell dormancy in brainR01CA252874 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI GHAJAR, CYRUS M · 2020 to 2024
$2.4M
Chemotherapy-driven evolution of the vascular secretome and its role in therapeutic resistanceR01CA249528 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI GHAJAR, CYRUS M · 2021 to 2025
$2.0M
Lymph node regulation of metastatic fitness and reemergenceF99CA234840 · NCI · UNIVERSITY OF WASHINGTON · PI LIM, ANDREA RACHEL · 2018 to 2019
$79k
NCI NIH HHS F99 CA234840NCI NIH HHS R01 CA249528NCI NIH HHS R01 CA252874NCI NIH HHS U54 CA193461
6 · The paper itself

Abstract

Disseminated tumor cells (DTCs) spread systemically yet distinct patterns of metastasis indicate a range of tissue susceptibility to metastatic colonization. Distinctions between permissive and suppressive tissues are still being elucidated at cellular and molecular levels. Although there is a growing appreciation for the role of the microenvironment in regulating metastatic success, we have a limited understanding of how diverse tissues regulate DTC dormancy, the state of reversible quiescence and subsequent awakening thought to contribute to delayed relapse. Several themes of microenvironmental regulation of dormancy are beginning to emerge, including vascular association, co-option of pre-existing niches, metabolic adaptation, and immune evasion, with tissue-specific nuances. Conversely, DTC awakening is often associated with injury or inflammation-induced activation of the stroma, promoting a proliferative environment with DTCs following suit. We review what is known about tissue-specific regulation of tumor dormancy on a tissue-by-tissue basis, profiling major metastatic organs including the bone, lung, brain, liver, and lymph node. An aerial view of the barriers to metastatic growth may reveal common targets and dependencies to inform the therapeutic prevention of relapse.

Indexed as

Disease SusceptibilityTumor MicroenvironmentAnimalsDisease ManagementHumansNeoplasmsRecurrenceDisseminated tumor cell dormancyDormant nicheMetastasisMicroenvironmentQuiescence

Identifiers

PMID33979673
PMCPMC9595433
OpenAlexW3161880773

What Socratic 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 Socratic graph.