Evidence map›Paper›PMID 36980644›Full record

ArticleCancers2023

MUG CCArly: A Novel Autologous 3D Cholangiocarcinoma Model Presents an Increased Angiogenic Potential.

Silke Schrom, Florian Kleinegger, Ines Anders, Thomas Hebesberger, Christina Karner, Laura Liesinger, Ruth Birner-Gruenberger, Wilfried Renner, Martin Pichler, Regina Grillari and 2 more

Open access · goldFull text read
In one paragraph

Article in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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 at 4 institutions in 2 countries.

Silke SchromDivision of Biomedical Research, Medical University of Graz, 8036 Graz, Austria.ORCID 0000-0003-3795-6519
Florian KleineggerDiagnostic and Research Institute of Pathology, Medical University of Graz, 8036 Graz, Austria.
Ines AndersDivision of Biomedical Research, Medical University of Graz, 8036 Graz, Austria.
Thomas HebesbergerDivision of Biomedical Research, Medical University of Graz, 8036 Graz, Austria.
Christina KarnerDivision of Biomedical Research, Medical University of Graz, 8036 Graz, Austria.ORCID 0000-0001-7088-3046
Laura LiesingerDiagnostic and Research Institute of Pathology, Medical University of Graz, 8036 Graz, Austria.
Ruth Birner-GruenbergerDiagnostic and Research Institute of Pathology, Medical University of Graz, 8036 Graz, Austria.ORCID 0000-0003-3950-0312
Wilfried RennerClinical Institute of Medical and Chemical Laboratory Diagnostics, Medical University of Graz, 8036 Graz, Austria.ORCID 0000-0002-6199-4382
Martin PichlerBiotechMed-Graz, 8010 Graz, Austria.ORCID 0000-0002-8701-9462
Regina GrillariEvercyte GmbH, 1190 Vienna, Austria.
Ariane AigelsreiterDiagnostic and Research Institute of Pathology, Medical University of Graz, 8036 Graz, Austria.
Beate RinnerDivision of Biomedical Research, Medical University of Graz, 8036 Graz, Austria.
Medical University of Graz · ATTU Wien · ATEvercyte (Austria) · ATUniversity Hospital Augsburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cholangiocarcinoma (CCA) are characterized by their desmoplastic and hypervascularized tumor microenvironment (TME), which is mainly composed of tumor cells and cancer-associated fibroblasts (CAFs). CAFs play a pivotal role in general and CCA tumor progression, angiogenesis, metastasis, and the development of treatment resistance. To our knowledge, no continuous human in vivo-like co-culture model is available for research. Therefore, we aimed to establish a new model system (called MUG CCArly) that mimics the desmoplastic microenvironment typically seen in CCA. Proteomic data comparing the new CCA tumor cell line with our co-culture tumor model (CCTM) indicated a higher gene expression correlation of the CCTM with physiological CCA characteristics. A pro-angiogenic TME that is typically observed in CCA could also be better simulated in the CCTM group. Further analysis of secreted proteins revealed CAFs to be the main source of these angiogenic factors. Our CCTM MUG CCArly represents a new, reproducible, and easy-to-handle 3D CCA model for preclinical studies focusing on CCA-stromal crosstalk, tumor angiogenesis, and invasion, as well as the immunosuppressive microenvironment and the involvement of CAFs in the way that drug resistance develops.

Indexed as

cancer-associated fibroblastsco-culture tumor modelproteomicsspheroidtumor microenvironment

Identifiers

PMID36980644
PMCPMC10046314
OpenAlexW4324142885

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read65
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.