Evidence map›Paper›PMID 32853629›Full record

ReviewPharmacology & therapeutics2021

Tumor organoid models in precision medicine and investigating cancer-stromal interactions.

Ren Xu, Xiaotao Zhou, Shike Wang, Christine Trinkle

Open access · greenAbstract readReview
In one paragraph

Review in Pharmacology & therapeutics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

76 citing papers in PubMed, 136 citations in OpenAlex.

  1. Review
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  5. Tumor organoid-immune cell co-culture systems for precision oncology.Frontiers in cell and developmental biology · 2026
    Review
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  8. Article
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  16. Advances and challenges in human 3D solid tumor models.Advanced functional materials · 2025
    Article
  17. Review
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  20. Review

16 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

4 authors at 1 institution in 1 country.

Ren XuDepartment of Pharmacology and Nutritional Sciences, University of Kentucky, Lexington, KY 40536, USA; Markey Cancer Center, University of Kentucky, Lexington, KY 40508, USA. Electronic address: ren.xu2010@uky.edu.
Xiaotao ZhouMarkey Cancer Center, University of Kentucky, Lexington, KY 40508, USA.
Shike WangMarkey Cancer Center, University of Kentucky, Lexington, KY 40508, USA.
Christine TrinkleDepartment of Mechanical Engineering, University of Kentucky, Lexington, KY, 40506, USA.
University of Kentucky · US

Funding

Roles of Hsp47 in Breast Cancer ProgressionR01CA207772 · NCI · UNIV OF ARKANSAS FOR MED SCIS · PI XU, REN · 2017 to 2025
$3.1M
Roles of RORalpha in breast cancer development and progressionR01CA215095 · NCI · UNIVERSITY OF KENTUCKY · PI XU, REN · 2017 to 2022
$1.7M
NCI NIH HHS R01 CA207772NCI NIH HHS R01 CA215095
6 · The paper itself

Abstract

Tumor development and progression require chemical and mechanical cues derived from cellular and non-cellular components in the tumor microenvironment, including the extracellular matrix (ECM), cancer-associated fibroblasts (CAFs), endothelial cells, and immune cells. Therefore, it is crucial to develop tissue culture models that can mimic in vivo cancer cell-ECM and cancer-stromal cell interactions. Three-dimensional (3D) tumor culture models have been widely utilized to study cancer development and progression. A recent advance in 3D culture is the development of patient-derived tumor organoid (PDO) models from primary human cancer tissue. PDOs maintain the heterogeneity of the primary tumor, which makes them more relevant for identifying therapeutic targets and verifying drug response. Other significant advances include development of 3D co-culture assays to investigate cell-cell interactions and tissue/organ morphogenesis, and microfluidic technology that can be integrated into 3D culture to mimic vasculature and blood flow. These advances offer spatial and temporal insights into cancer cell-stromal interactions and represent novel techniques to study tumor progression and drug response. Here, we summarize the recent progress in 3D culture and tumor organoid models, and discuss future directions and the potential of utilizing these models to study cancer-stromal interactions and direct personalized treatment.

Indexed as

NeoplasmsPrecision MedicineCell CommunicationHumansModels, BiologicalOrganoidsStromal CellsTumor Cells, CulturedTumor MicroenvironmentDrug screeningExtracellular matrixPatient-derived organoidPersonalized treatmentThree-dimensional tissue cultureTumor microenvironment

Identifiers

PMID32853629
PMCPMC7855432
OpenAlexW3080612021

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.