Evidence map›Paper›PMID 31488816›Full record

ArticleNature communications2019

Patient-derived lung cancer organoids as in vitro cancer models for therapeutic screening.

Minsuh Kim, Hyemin Mun, Chang Oak Sung, Eun Jeong Cho, Hye-Joon Jeon, Sung-Min Chun, Da Jung Jung, Tae Hoon Shin, Gi Seok Jeong, Dong Kwan Kim and 6 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05304741 (Drug Screening of Patient-derived Organoids From Advanced/Recurrent/Metastatic Colorectal Cancer Culture to Personalized Therapy, an Exploratory Research), which is not on this map. Cited by 497 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
497citing papers in PubMed, 3 pooled it
35.3field-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.

NCT05304741 unknown statusnot on this mapstarted 2020, after this paper: background citation

Drug Screening of Patient-derived Organoids From Advanced/Recurrent/Metastatic Colorectal Cancer Culture to Personalized Therapy, an Exploratory Research

Typeobservational_patient_registrySponsorChongqing University Cancer HospitalRan2020 to 2023Enrolled30ConditionsColorectal Cancer
3 · Its place in the literature

Who cites it

497 citing papers in PubMed, 3 syntheses or guidelines pooled it, 793 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
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  15. New developments and applications of human organoids.Nature reviews. Molecular cell biology · 2026
    Review
  16. Review
  17. Organoid technology in cancer research.Molecular biomedicine · 2026
    Review
  18. Article
  19. Article
  20. Article

437 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

16 authors at 3 institutions in 2 countries.

Minsuh KimAsan Center for Cancer Genome Discovery, Asan Institute for Life Sciences, Seoul, South Korea.
Hyemin MunAsan Center for Cancer Genome Discovery, Asan Institute for Life Sciences, Seoul, South Korea.
Chang Oak SungAsan Center for Cancer Genome Discovery, Asan Institute for Life Sciences, Seoul, South Korea.
Eun Jeong ChoAsan Center for Cancer Genome Discovery, Asan Institute for Life Sciences, Seoul, South Korea.ORCID http://orcid.org/0000-0001-9718-8473
Hye-Joon JeonAsan Center for Cancer Genome Discovery, Asan Institute for Life Sciences, Seoul, South Korea.
Sung-Min ChunAsan Center for Cancer Genome Discovery, Asan Institute for Life Sciences, Seoul, South Korea.
Da Jung JungBiomedical Engineering Research Center, Asan Institute for Life Sciences, Seoul, South Korea.ORCID http://orcid.org/0000-0002-5167-7738
Tae Hoon ShinBiomedical Engineering Research Center, Asan Institute for Life Sciences, Seoul, South Korea.ORCID http://orcid.org/0000-0002-3963-6773
Gi Seok JeongBiomedical Engineering Research Center, Asan Institute for Life Sciences, Seoul, South Korea.
Dong Kwan KimDepartment of Thoracic Surgery, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.
Eun Kyung ChoiDepartment of Radiation Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.
Seong-Yun JeongDepartment of Radiation Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.
Alison M TaylorDepartment of Medical Oncology and Center for Cancer-Genome Discovery, Dana-Farber Cancer Institute and Department of Pathology, Harvard Medical School, Boston, MA, USA.
Sejal JainDepartment of Medical Oncology and Center for Cancer-Genome Discovery, Dana-Farber Cancer Institute and Department of Pathology, Harvard Medical School, Boston, MA, USA.
Matthew MeyersonDepartment of Medical Oncology and Center for Cancer-Genome Discovery, Dana-Farber Cancer Institute and Department of Pathology, Harvard Medical School, Boston, MA, USA.ORCID http://orcid.org/0000-0002-9133-8108
Se Jin JangAsan Center for Cancer Genome Discovery, Asan Institute for Life Sciences, Seoul, South Korea. jangsejin@amc.seoul.kr.
Asan Medical Center · KRUlsan College · KRHarvard University · US

Funding

NKX2-1 Enhancer Amplification and Lineage Addiction in Lung AdenocarcinomaR35CA197568 · NCI · DANA-FARBER CANCER INST · PI Matthew L. Meyerson · 2015 to 2026
$12.4M
NCI NIH HHS R35 CA197568
6 · The paper itself

Abstract

Lung cancer shows substantial genetic and phenotypic heterogeneity across individuals, driving a need for personalised medicine. Here, we report lung cancer organoids and normal bronchial organoids established from patient tissues comprising five histological subtypes of lung cancer and non-neoplastic bronchial mucosa as in vitro models representing individual patient. The lung cancer organoids recapitulate the tissue architecture of the primary lung tumours and maintain the genomic alterations of the original tumours during long-term expansion in vitro. The normal bronchial organoids maintain cellular components of normal bronchial mucosa. Lung cancer organoids respond to drugs based on their genomic alterations: a BRCA2-mutant organoid to olaparib, an EGFR-mutant organoid to erlotinib, and an EGFR-mutant/MET-amplified organoid to crizotinib. Considering the short length of time from organoid establishment to drug testing, our newly developed model may prove useful for predicting patient-specific drug responses through in vitro patient-specific drug trials.

Indexed as

Drug Screening Assays, AntitumorAnimalsB7-H1 AntigenEarly Detection of CancerGenomicsHumansLung NeoplasmsMiceMice, Inbred NODMice, SCIDOrganoidsPrecision MedicineXenograft Model Antitumor AssaysB7-H1 AntigenCd274 protein, mouse

Identifiers

PMID31488816
PMCPMC6728380
OpenAlexW2971872568

What OpenQuestion holds

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LicenceCC BY
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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.