Evidence map›Paper›PMID 41403018›Full record

ArticleAnnals of medicine2025

Patient-derived organoids based on targeted biopsy of primary prostate cancer: development, identification, and drug screening.

Jiajun Qian, Shan Peng, Jie Gao, Yao Fu, Haifeng Huang, Cheng Wu, Weidong Gan, Xuefeng Qiu, Hongqian Guo

Abstract read
In one paragraph

Article in Annals of medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. 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

9 authors.

Jiajun QianDepartment of Urology, Affiliated Drum Tower Hospital, Medical School of Nanjing University, Nanjing, China.
Shan PengDepartment of Pathology, Affiliated Drum Tower Hospital, Medical School of Nanjing University, Nanjing, China.
Jie GaoDepartment of Urology, Affiliated Drum Tower Hospital, Medical School of Nanjing University, Nanjing, China.
Yao FuDepartment of Pathology, Affiliated Drum Tower Hospital, Medical School of Nanjing University, Nanjing, China.
Haifeng HuangDepartment of Urology, Affiliated Drum Tower Hospital, Medical School of Nanjing University, Nanjing, China.
Cheng WuDepartment of the Comprehensive Cancer Centre, Affiliated Drum Tower Hospital, Medical School of Nanjing University, Nanjing, China.
Weidong GanDepartment of Urology, Affiliated Drum Tower Hospital, Medical School of Nanjing University, Nanjing, China.
Xuefeng QiuDepartment of Urology, Affiliated Drum Tower Hospital, Medical School of Nanjing University, Nanjing, China.
Hongqian GuoDepartment of Urology, Affiliated Drum Tower Hospital, Medical School of Nanjing University, Nanjing, China.ORCID 0000-0002-3121-5157

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo develop patient-derived organoids (PDOs) using biopsied tissue of primary prostate cancer (PCa).

methodsFresh tumour tissues of PCa were obtained from patients who underwent targeted biopsy in our centre for the culture of PDOs. Hematoxylin-Eosin (H & E) and immunohistochemical staining were used to determine the histology of the cultured PDOs, using the parental tumours as the reference. Whole exome sequencing (WES) was conducted to verify the genetic conservation of PDOs, using the parental tumours as the reference. Drug screening was carried out to test the feasibility of PDOs as preclinical models.

resultsH & E and immunohistochemical staining indicated similar pathologic features between our developed PDOs and the parental tumours. WES also demonstrated similar somatic mutations, base substitutions and copy number variations between PDOs and the parental tumours. Drug screening results showed heterogeneity of the cultured PDOs to enzalutamide, docetaxel, and olaparib.

conclusionPDOs can be successfully developed based on targeted biopsy of primary PCa, which may be an optimal preclinical model to predict treatment response in the era of precision medicine.

Indexed as

Antineoplastic AgentsOrganoidsProstatic NeoplasmsAgedBenzamidesBiopsyDNA Copy Number VariationsDocetaxelDrug Screening Assays, AntitumorExome SequencingHumansMaleMiddle AgedMutationNitrilesPhenylthiohydantoinAntineoplastic AgentsBenzamidesDocetaxelenzalutamideNitrilesolaparibPhenylthiohydantoinPhthalazinesPiperazinesorganoidsprecise medicineprimaryprostate cancertargeted biopsy

Identifiers

PMID41403018
PMCPMC12713212

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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.