Evidence map›Paper›PMID 40624315›Full record

ArticleScientific reports2025

Head and neck tumor organoid grown under simplified media conditions model tumor biology and chemoradiation responses.

Weilin Li, Michiya Nishino, Eric Reed, Dipikaa Akshinthala, Hamdan Ahmed Pasha, Erik S Anderson, Ling Huang, Hannah Hebestreit, Stefano Monti, Ernest D Gomez and 2 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Organoids for disease modeling and treatment: state-of-the-art.Experimental hematology & oncology · 2026
    Review
  5. Review
  6. 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

12 authors.

Weilin LiLaboratory of Cancer Biology and Genetics, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, 20892, USA.
Michiya NishinoDepartment of Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, 02215, USA.
Eric ReedDepartment of Medicine, Albert Einstein College of Medicine, Bronx, New York, 10461, USA.
Dipikaa AkshinthalaLaboratory of Cancer Biology and Genetics, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, 20892, USA.
Hamdan Ahmed PashaDepartment of Surgery, Section of Otolaryngology/Head and Neck Surgery, Aga Khan University, Karachi, 74800, Pakistan.
Erik S AndersonDepartment of Radiation Oncology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, 02215, USA.
Ling HuangPancreatic Cancer Center, Henry Ford Health, Detroit, MI, 48202, USA.
Hannah HebestreitDepartment of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, 02215, USA.
Stefano MontiDepartment of Medicine, Computational Biomedicine Section, Boston University Chobanian and Avedisian School of Medicine, Boston, MA, 02118, USA.
Ernest D GomezDivision of Otolaryngology/Head and Neck Surgery, Beth Israel Deaconess Medical Center, Boston, MA, 02215, USA.
Scharukh M JalisiDivision of Otolaryngology/Head and Neck Surgery, Beth Israel Deaconess Medical Center, Boston, MA, 02215, USA.
Senthil K MuthuswamyLaboratory of Cancer Biology and Genetics, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, 20892, USA. senthil.muthuswamy@nih.gov.

Funding

System-Level Analyses of Multi-Omics Data to Reveal Mechanisms of Head & Neck CancerR01DE031831 · NIDCR · BOSTON UNIVERSITY MEDICAL CAMPUS · PI MONTI, STEFANO · 2022 to 2024
$1.3M
NIDCR NIH HHS R01 DE031831
6 · The paper itself

Abstract

Head and neck squamous cell carcinoma (HNSCC) is a prevalent and often fatal malignancy associated with significant treatment-related toxicity. There is an urgent need for a preclinical model to assess therapeutic options and guide clinical decision-making. To define conditions for establishing patient-derived organoid (PDO) models that faithfully recapitulate morphological, histopathological, and genomic characteristics of HNSCC patients and can predict radiation and chemotherapy responses in patients, PDOs were generated from a group of HNSCC patients. The morphological, histological, mutational, and biological characteristics and treatment responses were evaluated. We demonstrate that the PDOs closely resemble resected tumors from which they were derived with respect to histopathology, differentiation state markers, p16 status, and mutation profiling. We observe patient-to-patient variation in cell proliferation rates. Additionally, they exhibit differential responses to radiotherapy and chemotherapy, which were examined using a cell viability assay. This methodology offers potential for drug screening in a pre-clinical context with the potential to mirror clinical outcomes. Our WNT-free growth conditions maintained the differentiation status of PDOs and enabled rapid assessment of drug response and the development of new models to identify new treatment options for head and neck cancer patients.

Indexed as

ChemoradiotherapyHead and Neck NeoplasmsOrganoidsSquamous Cell Carcinoma of Head and NeckCell ProliferationCell SurvivalFemaleHumansMaleMutation

Identifiers

PMID40624315
PMCPMC12234821

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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.