Evidence map›Paper›PMID 27738841›Full record

ArticleBiomechanics and modeling in mechanobiology2017

Effects of flowing RBCs on adhesion of a circulating tumor cell in microvessels.

L L Xiao, Y Liu, S Chen, B M Fu

Open access · greenAbstract read
In one paragraph

Article in Biomechanics and modeling in mechanobiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.3field-weighted citation impact, top 9% 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

22 citing papers in PubMed, 58 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Tumor Metastasis in the Microcirculation.Advances in experimental medicine and biology · 2026
    Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Immunoregulation role of the erythroid cells.Frontiers in immunology · 2024
    Review
  12. A method for real-time mechanical characterisation of microcapsules.Biomechanics and modeling in mechanobiology · 2023
    Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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

4 authors at 3 institutions in 3 countries.

L L XiaoSchool of Aerospace Engineering and Applied Mechanics, Tongji University, Shanghai, China.
Y LiuDepartment of Mechanical Engineering, The Hong Kong Polytechnic University, Hung Hom, Hong Kong, China.
S ChenSchool of Aerospace Engineering and Applied Mechanics, Tongji University, Shanghai, China. schen_tju@tongji.edu.cn.
B M FuDepartment of Biomedical Engineering, The City College of the City University of New York, New York, NY, USA.
Tongji University · CNCity College of New York · USHong Kong Polytechnic University · HK

Funding

Tumor Cell Arrest and Adhesion in the MicrocirculationSC1CA153325 · NCI · CITY COLLEGE OF NEW YORK · PI FU, BINGMEI M. · 2010 to 2014
$750k
NCI NIH HHS SC1 CA153325
6 · The paper itself

Abstract

Adhesion of circulating tumor cells (CTCs) to the microvessel wall largely depends on the blood hydrodynamic conditions, one of which is the blood viscosity. Since blood is a non-Newtonian fluid, whose viscosity increases with hematocrit, in the microvessels at low shear rate. In this study, the effects of hematocrit, vessel size, flow rate and red blood cell (RBC) aggregation on adhesion of a CTC in the microvessels were numerically investigated using dissipative particle dynamics. The membrane of cells was represented by a spring-based network connected by elastic springs to characterize its deformation. RBC aggregation was modeled by a Morse potential function based on depletion-mediated assumption, and the adhesion of the CTC to the vessel wall was achieved by the interactions between receptors and ligands at the CTC and those at the endothelial cells forming the vessel wall. The results demonstrated that in the microvessel of [Formula: see text] diameter, the CTC has an increasing probability of adhesion with the hematocrit due to a growing wall-directed force, resulting in a larger number of receptor-ligand bonds formed on the cell surface. However, with the increase in microvessel size, an enhanced lift force at higher hematocrit detaches the initial adherent CTC quickly. If the microvessel is comparable to the CTC in diameter, CTC adhesion is independent of Hct. In addition, the velocity of CTC is larger than the average blood flow velocity in smaller microvessels and the relative velocity of CTC decreases with the increase in microvessel size. An increased blood flow resistance in the presence of CTC was also found. Moreover, it was found that the large deformation induced by high flow rate and the presence of aggregation promote the adhesion of CTC.

Indexed as

Models, BiologicalBlood Flow VelocityCell AdhesionComputer SimulationErythrocytesHematocritHumansMicrovesselsNeoplastic Cells, CirculatingAdhesionAggregationCirculating tumor cellDissipative particle dynamicsRed blood cell

Identifiers

PMID27738841
PMCPMC5352497
OpenAlexW2530445571

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.