Evidence map›Paper›PMID 40275403›Full record

ArticleJournal of experimental & clinical cancer research : CR2025

Advanced organoid models for targeting Kras-driven lung adenocarcinoma in drug discovery and combination therapy.

İsa Taş, Ruben Jacobs, Juliane Albrecht, Sebastian A Barrientos, Josephine Åberg, Wondossen Sime, Hans Brunnström, Helena Persson, Julhash U Kazi, Ramin Massoumi

Abstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Organoids glimpse: the nexus for diverse tumor heterogeneity.Frontiers in cell and developmental biology · 2026
    Review
  4. Emerging technologies and current challenges in intratumoral microbiota research.Frontiers in cellular and infection microbiology · 2025
    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

10 authors.

İsa TaşDepartment of Laboratory Medicine, Division of Translational Cancer Research, Lund University, Lund, Sweden.
Ruben JacobsDepartment of Laboratory Medicine, Division of Translational Cancer Research, Lund University, Lund, Sweden.
Juliane AlbrechtDepartment of Clinical Sciences Lund, Division of Oncology, Lund University, Lund, Sweden.
Sebastian A BarrientosDepartment of Laboratory Medicine, Division of Translational Cancer Research, Lund University, Lund, Sweden.
Josephine ÅbergDepartment of Laboratory Medicine, Division of Translational Cancer Research, Lund University, Lund, Sweden.
Wondossen SimeDepartment of Laboratory Medicine, Division of Translational Cancer Research, Lund University, Lund, Sweden.
Hans BrunnströmDepartment of Clinical Sciences Lund, Division of Pathology, Lund University, Lund, Sweden.
Helena PerssonDepartment of Clinical Sciences Lund, Division of Oncology, Lund University, Lund, Sweden.
Julhash U KaziDepartment of Laboratory Medicine, Division of Translational Cancer Research, Lund University, Lund, Sweden.
Ramin MassoumiDepartment of Laboratory Medicine, Division of Translational Cancer Research, Lund University, Lund, Sweden. ramin.massoumi@med.lu.se.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLung cancer remains one of the most challenging diseases to treat due to its heterogeneity. Kirsten Rat Sarcoma Viral Oncogene Homolog (KRAS) mutations are genetic drivers in numerous cancer types including lung adenocarcinoma (LUAD). Despite recent advances in KRAS-targeted therapies, treatment resistance and limited therapeutic options necessitate advanced preclinical models, such as organoids, to identify personalized cancer therapies by screening novel therapeutic strategies and synergistic drug combinations.

resultsWe established LUAD in genetically engineered mouse (GEM) models of Kras

conclusionWe successfully developed LUAD organoids harboring Kras mutations and identified multiple potential therapeutic agents targeting these cells. Furthermore, we demonstrated the effectiveness of a DNMT inhibitor-based combination therapy, presenting a promising strategy for this challenging lung cancer subtype.

Indexed as

Adenocarcinoma of LungAntineoplastic Combined Chemotherapy ProtocolsDrug DiscoveryLung NeoplasmsOrganoidsProto-Oncogene Proteins p21(ras)AnimalsDisease Models, AnimalHumansMiceMutationHras protein, mouseKRAS protein, humanProto-Oncogene Proteins p21(ras)DecitabineKras G12VLung adenocarcinomaMidostaurinOrganoids

Identifiers

PMID40275403
PMCPMC12020293

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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.