Evidence map›Paper›PMID 36659831›Full record

ArticleJournal of gynecologic oncology2023

Preclinical investigation of patient-derived cervical cancer organoids for precision medicine.

Hyang Sook Seol, Ju Hee Oh, Eunhye Choi, SangMin Kim, Hyunki Kim, Eun Ji Nam

Open access · diamondAbstract read
In one paragraph

Article in Journal of gynecologic oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 2 pooled it
6.7field-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

23 citing papers in PubMed, 2 syntheses or guidelines pooled it, 29 citations in OpenAlex.

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  14. Organoid technology in cervical cancer research.American journal of cancer research · 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

6 authors at 1 institution in 1 country.

Hyang Sook Seol *Department of Obstetrics and Gynecology, Institute of Women's Medical Life Science, Yonsei Cancer Center, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.ORCID 0000-0002-6200-8433
Ju Hee Oh *Department of Obstetrics and Gynecology, Institute of Women's Medical Life Science, Yonsei Cancer Center, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.ORCID 0000-0003-2864-7677
Eunhye ChoiDepartment of Obstetrics and Gynecology, Institute of Women's Medical Life Science, Yonsei Cancer Center, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.ORCID 0000-0001-5206-1217
SangMin KimDepartment of Pathology, Yonsei University College of Medicine, Seoul, Korea.ORCID 0000-0002-4013-3540
Hyunki KimDepartment of Pathology, Yonsei University College of Medicine, Seoul, Korea.ORCID 0000-0003-2292-5584
Eun Ji NamDepartment of Obstetrics and Gynecology, Institute of Women's Medical Life Science, Yonsei Cancer Center, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea. NAHMEJ6@yuhs.ac.ORCID 0000-0003-0189-3560
Yonsei University · KR

Funding

National Research Foundation of Korea 2020R1A2B5B0100237113Yonsei University College of Medicine 6-2018-0053Yonsei University College of Medicine 6-2019-0166
6 · The paper itself

Abstract

objectiveAdvanced cervical cancer is still difficult to treat and in the case of recurrent cancer, it is desirable to utilize personalized treatment rather than uniform treatment because the type of recurrence is different for each individual. Therefore, this study aimed to establish a patient-derived organoid (PDO) platform to determine the effects of chemotherapy, radiation therapy, and targeted therapy in cervical cancer.

methodsWe established organoids from 4 patients with various types of cervical cancer. The histopathological and gene profiles of these organoid models were compared to determine their characteristics and the maintenance of the patient phenotype. Each type of organoid was also subjected to anticancer drug screening and radiation therapy to evaluate its sensitivity.

resultsWe established PDOs to recapitulate the main elements of the original patient tumors, including the DNA copy number and mutational profile. We selected 7 drugs that showed growth inhibition in cervical cancer organoids out of 171 using an Food and Drug Administration -approved drug library. Moreover, adenocarcinoma and large-cell neuroendocrine carcinoma showed resistance to radiation therapy. whereas squamous cell carcinoma and villoglandular carcinoma showed a significant response to radiotherapy.

conclusionOur results showed that patient-derived cervical cancer organoids can be used as a platform for drug and radiation sensitivity testing. These findings suggest that patient-derived cervical cancer organoids could be used as a personalized medicine platform and may provide the best treatment options for patients with various subtypes of cervical cancer.

Indexed as

AdenocarcinomaAntineoplastic AgentsCarcinoma, Squamous CellUterine Cervical NeoplasmsFemaleHumansNeoplasm Recurrence, LocalOrganoidsPrecision MedicineAntineoplastic AgentsCervical CancerOrganoidsRadiationTumor-Specific Drug Screening Tests

Identifiers

PMID36659831
PMCPMC10157333
OpenAlexW4313566500

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.