Evidence map›Paper›PMID 34240815›Full record

ArticleCancer medicine2021

Establishment of patient-derived organotypic tumor spheroid models for tumor microenvironment modeling.

Hye Kyung Hong, Nak Hyeon Yun, Ye-Lin Jeong, Jeehun Park, Junsang Doh, Woo Yong Lee, Yong Beom Cho

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.1field-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

24 citing papers in PubMed, 30 citations in OpenAlex.

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  7. Biomedical applications of organoids derived from the digestive system.Frontiers in cell and developmental biology · 2025
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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

7 authors at 3 institutions in 1 country.

Hye Kyung HongDepartment of Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.ORCID 0000-0002-4604-3765
Nak Hyeon YunDepartment of Health Sciences and Technology, SAIHST, Sungkyunkwan University, Seoul, Korea.
Ye-Lin JeongInstitute for Future Medicine, Samsung Medical Center, Seoul, Korea.
Jeehun ParkResearch Institute of Advanced Materials, Seoul National University, Seoul, Korea.
Junsang DohResearch Institute of Advanced Materials, Seoul National University, Seoul, Korea.
Woo Yong LeeDepartment of Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Yong Beom ChoDepartment of Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Samsung Medical Center · KRSeoul National University · KRSungkyunkwan University · KR

Funding

the Institute of Information & Communications Technology Planning & Evaluation (IITP) grant 2019-0-00047the Ministry of Trade, Industry and Energy (MOTIE) and Korea Institute for Advancement of Technology(KIAT) P0011266the National Research Foundation of Korea (NRF) grant 2020R1F1A1075646
6 · The paper itself

Abstract

Patient-derived cancer models that reconstitute the characteristics of the tumor microenvironment may facilitate efforts in precision immune-oncology and the discovery of effective anticancer therapies. Organoids that have recently emerged as robust preclinical models typically contain tumor epithelial cells and lack the native tumor immune microenvironment. A patient-derived organotypic tumor spheroid (PDOTS) is a novel and innovative ex vivo system that retains key features of the native tumor immune microenvironment. Here, we established and characterized a series of colorectal cancer PDOTS models for use as a preclinical platform for testing effective immunotherapy and its combinations with other drugs. Partially dissociated (> 100 μm in diameter) tumor tissues were embedded in Matrigel-containing organoid media and subsequently formed into organoid structures within 3 to 7 days of culture. The success rate of growing PDOTS from fresh tissues was ~86%. Morphological analysis showed that the PDOTSs varied in size and structure. Immunofluorescence and flow cytometry analysis revealed that the PDOTSs retained autologous tumor-infiltrating lymphoid cells and tumor-infiltrating lymphoid cells were continually decreased through serial passages. Notably, PDOTSs from tumors from a high-level microsatellite instability-harboring patient were sensitive to anti-PD-1 or anti-PD-L1 antibodies. Our results demonstrate that the PDOTS model in which the tumor immune microenvironment is preserved may represent an advantageous ex vivo system to develop effective immune therapeutics.

Indexed as

B7-H1 AntigenCell Line, TumorColorectal NeoplasmsDrug Screening Assays, AntitumorHumansImmune Checkpoint InhibitorsMicrosatellite InstabilityPrimary Cell CultureProgrammed Cell Death 1 ReceptorSpheroids, CellularTumor Cells, CulturedTumor MicroenvironmentB7-H1 AntigenCD274 protein, humanImmune Checkpoint InhibitorsPDCD1 protein, humanProgrammed Cell Death 1 Receptorcolorectal cancerimmune therapeuticsorganotypic tumor spheroidpatient-derived cancer modeltumor microenvironment

Identifiers

PMID34240815
PMCPMC8366099
OpenAlexW3181184429

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.