Evidence map›Paper›PMID 24202395›Full record

ReviewNature medicine2013

Microenvironmental regulation of tumor progression and metastasis.

Daniela F Quail, Johanna A Joyce

2 registry-linked trialsOpen access · greenAbstract readReview
In one paragraph

Review in Nature medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 4,718 papers.

0numbers the graph read from it
0cells of the map it votes in
4,718citing papers in PubMed
121.7field-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.

NCT04634188 completednot on this mapstarted 2020, after this paper: background citation

Role and Value of Inflammatory Markers in Brain Tumors : A Case Controlled Study

Typeobservational_patient_registrySponsorUniversitas Sumatera UtaraRan2020 to 2020Enrolled35ConditionsBrain TumorArmsProcalcitonin
NCT06841172 phase3recruitingnot on this mapstarted 2025, after this paper: background citation

Continuation of First-line Therapy With Radiotherapy for Oligoprogression Versus Early Switch to Second-line Therapy in Oligoprogressive Hepatocellular Carcinoma (CROSS): a Multi-center, Randomized, Controlled, Open-label, Phase Ⅲ Trial

TypeinterventionalSponsorShandong Cancer Hospital and InstituteRan2025 to 2028Enrolled132ConditionsOligoProgressive Metastatic Disease, Hepatocellular Carcinoma (HCC), Radiotherapy, Systemic TherapyArmsradiotherapy, Systemic therapy (Continuation of current first-line systemic therapy), Systemic therapy (Early switch to second-line systemic therapy)
3 · Its place in the literature

Who cites it

4,718 citing papers in PubMed, 7,973 citations in OpenAlex.

  1. Trial
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  9. Cell plasticity in cancer and therapy resistance.Experimental & molecular medicine · 2026
    Review
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  16. SPRED2 Negatively Regulates CD8Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
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4,658 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

2 authors at 1 institution in 1 country.

Daniela F QuailCancer Biology and Genetics Program, Memorial Sloan-Kettering Cancer Center, New York, New York, USA.
Johanna A Joyce
Memorial Sloan Kettering Cancer Center · US

Funding

Variability of Cellular Responses to Growth Factors and Drugs During TumorgenesisU54CA148967 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI ALTAN-BONNET, GREGOIRE · 2010 to 2014
$13.8M
Tumor Microenvironment Interactions in Brain TumorsU54CA126518 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI JOYCE, JOHANNA · 2006 to 2010
$6.1M
CIHRNCI NIH HHS U54 CA126518NCI NIH HHS U54 CA148967
6 · The paper itself

Abstract

Cancers develop in complex tissue environments, which they depend on for sustained growth, invasion and metastasis. Unlike tumor cells, stromal cell types within the tumor microenvironment (TME) are genetically stable and thus represent an attractive therapeutic target with reduced risk of resistance and tumor recurrence. However, specifically disrupting the pro-tumorigenic TME is a challenging undertaking, as the TME has diverse capacities to induce both beneficial and adverse consequences for tumorigenesis. Furthermore, many studies have shown that the microenvironment is capable of normalizing tumor cells, suggesting that re-education of stromal cells, rather than targeted ablation per se, may be an effective strategy for treating cancer. Here we discuss the paradoxical roles of the TME during specific stages of cancer progression and metastasis, as well as recent therapeutic attempts to re-educate stromal cells within the TME to have anti-tumorigenic effects.

Indexed as

Cell Cycle CheckpointsDisease ProgressionHumansImmunotherapyInflammationMacrophagesModels, BiologicalNeoplasm InvasivenessNeoplasm MetastasisNeoplasmsNeovascularization, PathologicStromal CellsTumor Microenvironment

Identifiers

PMID24202395
PMCPMC3954707
OpenAlexW2033278321

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.