Evidence map›Paper›PMID 40533468›Full record

ArticleBJC reports2025

Cytoskeleton imaging of colorectal and lung cancer spheroids using light sheet microscopy.

Sonia Prado-López, Massih Foroughipour, Klaus Becker, Seyed Meraaj Foroughipour, Lukas Weber, Heinz Wanzenboeck, Nika Sarem, Saiedeh Saghafi

Abstract read
In one paragraph

Article in BJC reports, 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. Article
  2. Article
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.

Sonia Prado-LópezResearch Unit of Nanoelectronic Devices, Institute of Solid State Electronics, Faculty of Electrical Engineering and Information Technology, TU Wien, Vienna, Austria. sonia.lopez@tuwien.ac.at.
Massih ForoughipourMeso-Aspheric Optics & LSFM Group, Institute of Solid State Electronics, Faculty of Electrical Engineering and Information Technology, TU Wien, Vienna, Austria.
Klaus BeckerMeso-Aspheric Optics & LSFM Group, Institute of Solid State Electronics, Faculty of Electrical Engineering and Information Technology, TU Wien, Vienna, Austria.
Seyed Meraaj ForoughipourMeso-Aspheric Optics & LSFM Group, Institute of Solid State Electronics, Faculty of Electrical Engineering and Information Technology, TU Wien, Vienna, Austria.
Lukas WeberMeso-Aspheric Optics & LSFM Group, Institute of Solid State Electronics, Faculty of Electrical Engineering and Information Technology, TU Wien, Vienna, Austria.
Heinz WanzenboeckResearch Unit of Nanoelectronic Devices, Institute of Solid State Electronics, Faculty of Electrical Engineering and Information Technology, TU Wien, Vienna, Austria.
Nika SaremMeso-Aspheric Optics & LSFM Group, Institute of Solid State Electronics, Faculty of Electrical Engineering and Information Technology, TU Wien, Vienna, Austria.
Saiedeh SaghafiMeso-Aspheric Optics & LSFM Group, Institute of Solid State Electronics, Faculty of Electrical Engineering and Information Technology, TU Wien, Vienna, Austria. saiedeh.saghafi@tuwien.ac.at.

Funding

Austria wirtschaftsservice AWS P2403385Österreichische Forschungsförderungsgesellschaft IRA-SME project ELEVATE (FFG Grant No. 895365)TU Wien Bibliothek Open Access Funding ProgrammeVienna Science and Technology Fund (WWTF) NXT22-001 and CS18-019
6 · The paper itself

Abstract

backgroundThree dimensional tumoral models are essential to study cancer biology as they better mimic the complexity of the tumoral masses in vivo. However, to study cancer 3D models' dynamics new technological approaches are required. Most of the deaths related to cancer are caused by metastasis but still many of the metastatic driving processes remain unknown. A fundamental player in the metastatic process is the cytoskeleton. The polymerization of actin monomers in filaments, known as F-actin, is crucial for cell motility. Also, it can be used to detect necrosis, since F-actin is exposed on necrotic cells due to the loss of the cell membrane's integrity. To date, studies of actin dynamics in cancer cells have primarily relied on simplistic 2D models and fluorescence microscopy.

methodsIn this paper, we propose combining light sheet fluorescence microscopy (LSFM) with colorectal cancer (CRC) and non-small cell lung carcinoma (NSCLC) spheroids to study F-actin distribution and exposition with minimal distortions.

resultsWe identified 6 different areas of F-actin intensity that could be correlated with the proliferative, senescence and necrotic zones previously described in cancer spheroid models in vitro.

conclusionsOur findings proved the power of the proposed LS meso aspheric optics approach to visualize and quantify F-actin in 3D cancer models with a high level of detail. Importantly, our findings also facilitate the assessment of the necrotic area's extent, clearing the path for improved anti-metastatic treatments and more accurate patient prognosis evaluation.

Identifiers

PMID40533468
PMCPMC12177031

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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.