Evidence map›Paper›PMID 30393286›Full record

ArticleMicromachines2017

The Viability of Single Cancer Cells after Exposure to Hydrodynamic Shear Stresses in a Spiral Microchannel: A Canine Cutaneous Mast Cell Tumor Model.

Dettachai Ketpun, Achariya Sailasuta, Thammawit Suwannaphan, Sudchaya Bhanpattanakul, Alongkorn Pimpin, Werayut Srituravanich, Witsaroot Sripumkhai, Wutthinan Jeamsaksiri, Prapruddee Piyaviriyakul

Open access · goldAbstract read
In one paragraph

Article in Micromachines, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

5 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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  5. 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

9 authors at 2 institutions in 2 countries.

Dettachai KetpunBiochemistry Unit, Department of Physiology, Faculty of Veterinary Science, Chulalongkorn University, Bangkok 10330, Thailand. dketpun@ntu.edu.sg.ORCID 0000-0002-0944-6389
Achariya SailasutaCompanion Animal Cancer-Research Unit (CAC-RU), Department of Pathology, Faculty of Veterinary Science, Chulalongkorn University, Bangkok 10330, Thailand. achariya.sa@chula.ac.th.
Thammawit SuwannaphanDepartment of Mechanical Engineering, Faculty of Engineering, Chulalongkorn University, Bangkok 10330, Thailand. Thammawit.Su@student.chula.ac.th.
Sudchaya BhanpattanakulCompanion Animal Cancer-Research Unit (CAC-RU), Department of Pathology, Faculty of Veterinary Science, Chulalongkorn University, Bangkok 10330, Thailand. Sudchaya.Bha@student.chula.ac.th.
Alongkorn PimpinCompanion Animal Cancer-Research Unit (CAC-RU), Department of Pathology, Faculty of Veterinary Science, Chulalongkorn University, Bangkok 10330, Thailand. alongkorn.p@chula.ac.th.
Werayut SrituravanichCompanion Animal Cancer-Research Unit (CAC-RU), Department of Pathology, Faculty of Veterinary Science, Chulalongkorn University, Bangkok 10330, Thailand. werayut.s@chula.ac.th.
Witsaroot SripumkhaiThai Microelectronic Centre, Ministry of Science and Technology, Chachoengsao 24000, Thailand. witsaroot.sripumkhai@nectec.or.th.
Wutthinan JeamsaksiriThai Microelectronic Centre, Ministry of Science and Technology, Chachoengsao 24000, Thailand. wutthinan.jeamsaksiri@nectec.or.th.ORCID 0000-0001-7616-0703
Prapruddee PiyaviriyakulBiochemistry Unit, Department of Physiology, Faculty of Veterinary Science, Chulalongkorn University, Bangkok 10330, Thailand. Prapruddee.P@chula.ac.th.
Chulalongkorn University · THMinistry of Science and Technology Thailand · TH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Our laboratory has the fundamental responsibility to study cancer stem cells (CSC) in various models of human and animal neoplasms. However, the major impediments that spike our accomplishment are the lack of universal biomarkers and cellular heterogeneity. To cope with these restrictions, we have tried to apply the concept of single cell analysis, which has hitherto been recommended throughout the world as an imperative solution pack for resolving such dilemmas. Accordingly, our first step was to utilize a predesigned spiral microchannel fabricated by our laboratory to perform size-based single cell separation using mast cell tumor (MCT) cells as a model. However, the impact of hydrodynamic shear stresses (HSS) on mechanical cell injury and viability in a spiral microchannel has not been fully investigated so far. Intuitively, our computational fluid dynamics (CFD) simulation has strongly revealed the formations of fluid shear stress (FSS) and extensional fluid stress (EFS) in the sorting system. The panel of biomedical assays has also disclosed cell degeneration and necrosis in the model. Therefore, we have herein reported the combinatorically detrimental effect of FSS and EFS on the viability of MCT cells after sorting in our spiral microchannel, with discussion on the possibly pathogenic mechanisms of HSS-induced cell injury in the study model.

Indexed as

hydrodynamic shear stressmast cell tumormicrofluidicsortingspiral microchannelviability

Identifiers

PMID30393286
PMCPMC6187537
OpenAlexW2780025357

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.