Evidence map›Paper›PMID 35773148›Full record

ReviewTrends in cancer2022

Immune organoids: from tumor modeling to precision oncology.

Vinh Dao, Kanako Yuki, Yuan-Hung Lo, Michitaka Nakano, Calvin J Kuo

Open access · greenAbstract readReview
In one paragraph

Review in Trends in cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
5.7field-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

47 citing papers in PubMed, 62 citations in OpenAlex.

  1. Review
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  3. Article
  4. Article
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  8. Article
  9. Article
  10. Tumor organoid-immune cell co-culture systems for precision oncology.Frontiers in cell and developmental biology · 2026
    Review
  11. Review
  12. Review
  13. Beyond Rodents: Alternative Animal Models in Colorectal Cancer Research.International journal of molecular sciences · 2025
    Review
  14. Bioprinted Organoids: An Innovative Engine in Biomedicine.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  15. Review
  16. Immune organoid for cancer immunotherapy.Acta pharmaceutica Sinica. B · 2025
    Review
  17. Review
  18. Review
  19. 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

5 authors at 2 institutions in 1 country.

Vinh DaoDepartment of Medicine, Division of Hematology, Stanford University School of Medicine, Stanford, CA, USA; Department of Medicine, Division of Oncology, Stanford University School of Medicine, Stanford, CA, USA.
Kanako YukiDepartment of Medicine, Division of Hematology, Stanford University School of Medicine, Stanford, CA, USA.
Yuan-Hung LoDepartment of Medicine, Division of Hematology, Stanford University School of Medicine, Stanford, CA, USA.
Michitaka NakanoDepartment of Medicine, Division of Hematology, Stanford University School of Medicine, Stanford, CA, USA.
Calvin J KuoDepartment of Medicine, Division of Hematology, Stanford University School of Medicine, Stanford, CA, USA. Electronic address: cjkuo@stanford.edu.
Stanford University · USStanford Medicine · US

Funding

UCSF Project 1U54CA224081 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Trever G Bivona, Jack Roth · 2017 to 2026
$12.9M
Regulation of actively proliferating and quiescent intestinal stem cellsU01DK085527 · NIDDK · STANFORD UNIVERSITY · PI KUO, CALVIN J · 2009 to 2023
$6.9M
Organoid-based Discovery of Oncogenic Drivers and Treatment Resistance MechanismsU01CA217851 · NCI · STANFORD UNIVERSITY · PI CURTIS, CHRISTINA N, JI, HANLEE P · 2017 to 2021
$4.7M
Immunotherapy Modeling in Organoids Co-preserving Tumor and Infiltrating Immune CompartmentsR01CA251514 · NCI · STANFORD UNIVERSITY · PI KUO, CALVIN J · 2021 to 2025
$3.2M
Program in Translational and Experimental HematologyT32HL120824 · NHLBI · STANFORD UNIVERSITY · PI MAJETI, RAVINDRA · 2014 to 2023
$2.4M
TRANSCRIPTION FACTORS IN INTESTINAL DIFFERENTIATION AND CANCERK00CA212433 · NCI · STANFORD UNIVERSITY · PI LO, YUAN-HUNG · 2017 to 2020
$345k
Functional characterization of novel oncogenic loci driving progression and immune response in gastrointestinal cancerK99CA263014 · NCI · STANFORD UNIVERSITY · PI LO, YUAN-HUNG · 2021 to 2022
$343k
NCI NIH HHS K00 CA212433NCI NIH HHS K99 CA263014NCI NIH HHS R01 CA251514NCI NIH HHS U01 CA217851NCI NIH HHS U54 CA224081NHLBI NIH HHS T32 HL120824NIDDK NIH HHS U01 DK085527
6 · The paper itself

Abstract

Cancer immunotherapies, particularly immune checkpoint inhibitors, are rapidly becoming standard-of-care for many cancers. The ascendance of immune checkpoint inhibitor treatment and limitations in the accurate prediction of clinical response thereof have provided significant impetus to develop preclinical models that can guide therapeutic intervention. Traditional organoid culture methods that exclusively grow tumor epithelium as patient-derived organoids are under investigation as a personalized platform for drug discovery and for predicting clinical efficacy of chemotherapies and targeted agents. Recently, the patient-derived tumor organoid platform has evolved to contain more complex stromal and immune compartments needed to assess immunotherapeutic efficacy. We review the different methodologies for developing a more holistic patient-derived tumor organoid platform and for modeling the native immune tumor microenvironment.

Indexed as

NeoplasmsOrganoidsHumansImmune Checkpoint InhibitorsPrecision MedicineTumor MicroenvironmentImmune Checkpoint Inhibitorsimmune checkpoint inhibitorsPatient-derived tumor organoidsprecision oncology

Identifiers

PMID35773148
PMCPMC9704769
OpenAlexW4283769337

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.