Evidence map›Paper›PMID 37769417›Full record

ArticleComputer methods and programs in biomedicine2023

Modeling critical interaction for metastasis between circulating tumor cells (CTCs) and platelets adhered to the capillary wall.

Miljan Milosevic, Vladimir Simic, Aleksandar Nikolic, Ning Shao, Chihiro Kawamura Hashimoto, Biana Godin, Fransisca Leonard, Xuewu Liu, Milos Kojic

Open access · greenAbstract read
In one paragraph

Article in Computer methods and programs in biomedicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

9 authors at 2 institutions in 2 countries.

Miljan MilosevicBioengineering Research and Development Center, BioIRC, Prvoslava Stojanovica 6, 34 000 Kragujevac, Serbia; Institute for Information Technologies, University of Kragujevac, Jovana Cvijica, 34 000 Kragujevac, Serbia; Belgrade Metropolitan University, Tadeuša Košćuška 63, 11158 Belgrade, Serbia.
Vladimir SimicBioengineering Research and Development Center, BioIRC, Prvoslava Stojanovica 6, 34 000 Kragujevac, Serbia; Institute for Information Technologies, University of Kragujevac, Jovana Cvijica, 34 000 Kragujevac, Serbia.
Aleksandar NikolicThe Institute for Artificial Intelligence Research and Development of Serbia, Fruskogorska 1, 21 000 Novi Sad, Serbia.
Ning ShaoHouston Methodist Research Institute, Department of Nanomedicine, 6670 Bertner Ave, Houston, TX 77030, United States.
Chihiro Kawamura HashimotoHouston Methodist Research Institute, Department of Nanomedicine, 6670 Bertner Ave, Houston, TX 77030, United States; Houston Methodist Research Institute, Department of Neurology, 6670 Bertner Ave, Houston, TX 77030, United States.
Biana GodinHouston Methodist Research Institute, Department of Nanomedicine, 6670 Bertner Ave, Houston, TX 77030, United States.
Fransisca LeonardHouston Methodist Research Institute, Department of Nanomedicine, 6670 Bertner Ave, Houston, TX 77030, United States; Houston Methodist Research Institute, Department of Neurology, 6670 Bertner Ave, Houston, TX 77030, United States.
Xuewu LiuHouston Methodist Research Institute, Department of Nanomedicine, 6670 Bertner Ave, Houston, TX 77030, United States.
Milos KojicBioengineering Research and Development Center, BioIRC, Prvoslava Stojanovica 6, 34 000 Kragujevac, Serbia; Houston Methodist Research Institute, Department of Nanomedicine, 6670 Bertner Ave, Houston, TX 77030, United States; Serbian Academy of Sciences and Arts, Kneza Mihaila 35, 11 000 Belgrade, Serbia.
Houston Methodist · USUniversity of Kragujevac · RS

Funding

Biophysical roles of pre-metastatic niche evolution on transport of circulating tumor cellsU01CA244107 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI KOJIC, MILOS, LEONARD, FRANSISCA · 2020 to 2024
$2.8M
NCI NIH HHS U01 CA244107
6 · The paper itself

Abstract

BACKGROUND AND

objectiveWe used a 2D fluid-solid interaction (FSI) model to investigate the critical conditions for the arrest of the CTCs traveling through the narrowed capillary with a platelet attached to the capillary wall. This computational model allows us to determine the deformations and the progression of the passage of the CTC through different types of microvessels with platelet included.

methodsThe modeling process is obtained using the strong coupling approach following the remeshing procedure. Also, the 1D FE rope element for simulating active ligand-receptor bonds is implemented in our computational tool (described below).

resultsA relationship between the CTCs properties (size and stiffness), the platelet size and stiffness, and the ligand-receptor interaction intensity, on one side, and the time in contact between the CTCs and platelet and conditions for the cell arrest, on the other side, are determined. The model is further validated in vitro by using a microfluidic device with metastatic breast tumor cells.

conclusionsThe computational framework that is presented, with accompanying results, can be used as a powerful tool to study biomechanical conditions for CTCs arrest in interaction with platelets, giving a prognosis of disease progression.

Indexed as

Neoplastic Cells, CirculatingBreastCapillariesHumansLigandsPrognosisLigandsConditions for cell arrestCTC-platelet interactionFinite element analysisFluid-solid interactionIncompressible deformations of solidMetastasis

Identifiers

PMID37769417
PMCPMC10795320
OpenAlexW4386625270

What OpenQuestion holds

Textmetadata
LicenceTDM
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.