Evidence map›Paper›PMID 38654067›Full record

ArticleScientific reports2024

A pancreatic cancer organoid-in-matrix platform shows distinct sensitivities to T cell killing.

Anton Lahusen, Jierui Cai, Reinhold Schirmbeck, Anton Wellstein, Alexander Kleger, Thomas Seufferlein, Tim Eiseler, Yuan-Na Lin

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.4field-weighted citation impact, top 6% 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

14 citing papers in PubMed, 12 citations in OpenAlex.

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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

8 authors at 2 institutions in 2 countries.

Anton LahusenDepartment of Internal Medicine I, Gastroenterology, Endocrinology, Nephrology, Nutrition and Metabolism, Ulm University Hospital, Albert Einstein Allee 23, 89081, Ulm, Germany.
Jierui CaiDepartment of Internal Medicine I, Gastroenterology, Endocrinology, Nephrology, Nutrition and Metabolism, Ulm University Hospital, Albert Einstein Allee 23, 89081, Ulm, Germany.
Reinhold SchirmbeckDepartment of Internal Medicine I, Gastroenterology, Endocrinology, Nephrology, Nutrition and Metabolism, Ulm University Hospital, Albert Einstein Allee 23, 89081, Ulm, Germany.
Anton WellsteinLombardi Comprehensive Cancer Center, Georgetown University, 3970 Reservoir Road NW, Washington, DC, 20007, USA.
Alexander KlegerDepartment of Internal Medicine I, Gastroenterology, Endocrinology, Nephrology, Nutrition and Metabolism, Ulm University Hospital, Albert Einstein Allee 23, 89081, Ulm, Germany.
Thomas SeufferleinDepartment of Internal Medicine I, Gastroenterology, Endocrinology, Nephrology, Nutrition and Metabolism, Ulm University Hospital, Albert Einstein Allee 23, 89081, Ulm, Germany.
Tim EiselerDepartment of Internal Medicine I, Gastroenterology, Endocrinology, Nephrology, Nutrition and Metabolism, Ulm University Hospital, Albert Einstein Allee 23, 89081, Ulm, Germany.
Yuan-Na LinDepartment of Internal Medicine I, Gastroenterology, Endocrinology, Nephrology, Nutrition and Metabolism, Ulm University Hospital, Albert Einstein Allee 23, 89081, Ulm, Germany. yuanna.lin@uni-ulm.de.
University Hospital Ulm · DEGeorgetown University · US

Funding

Deutsche Forschungsgemeinschaft LI 2547/6-1
6 · The paper itself

Abstract

Poor treatment responses of pancreatic ductal adenocarcinoma (PDAC) are in large part due to tumor heterogeneity and an immunosuppressive desmoplastic tumor stroma that impacts interactions with cells in the tumor microenvironment (TME). Thus, there is a pressing need for models to probe the contributions of cellular and noncellular crosstalk. Organoids are promising model systems with the potential to generate a plethora of data including phenotypic, transcriptomic and genomic characterization but still require improvements in culture conditions mimicking the TME. Here, we describe an INTERaction with Organoid-in-MatriX ("InterOMaX") model system, that presents a 3D co-culture-based platform for investigating matrix-dependent cellular crosstalk. We describe its potential to uncover new molecular mechanisms of T cell responses to murine KPC (LSL-Kras

Indexed as

Carcinoma, Pancreatic DuctalOrganoidsPancreatic NeoplasmsT-LymphocytesTumor MicroenvironmentAnimalsCell Line, TumorCoculture TechniquesHumansMice

Identifiers

PMID38654067
PMCPMC11039640
OpenAlexW4395029922

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.