Evidence map›Paper›PMID 25314577›Full record

ArticlePloS one2014

Human equilibrative nucleoside transporter-1 knockdown tunes cellular mechanics through epithelial-mesenchymal transition in pancreatic cancer cells.

Yeonju Lee, Eugene J Koay, Weijia Zhang, Lidong Qin, Dickson K Kirui, Fazle Hussain, Haifa Shen, Mauro Ferrari

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

11 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Origin of cells and network information.World journal of stem cells · 2015
    Article
  11. 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

8 authors at 4 institutions in 1 country.

Yeonju LeeDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, Texas, United States of America.
Eugene J KoayDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, Texas, United States of America; Department of Radiation Oncology, M. D. Anderson Cancer Center, Houston, Texas, United States of America.
Weijia ZhangDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, Texas, United States of America.
Lidong QinDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, Texas, United States of America; Department of Cell and Developmental Biology, Weill Cornell Medical College, New York, New York, United States of America.
Dickson K KiruiDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, Texas, United States of America.
Fazle HussainDepartment of Mechanical Engineering, Texas Tech University, Lubbock, Texas, United States of America.
Haifa ShenDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, Texas, United States of America; Department of Cell and Developmental Biology, Weill Cornell Medical College, New York, New York, United States of America.
Mauro FerrariDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, Texas, United States of America; Department of Medicine, Weill Cornell Medical College, New York, New York, United States of America.
Cornell University · USHouston Methodist · USTexas Tech University · USThe University of Texas MD Anderson Cancer Center · US

Funding

Texas Center for Cancer NanomedicineU54CA151668 · NCI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI FERRARI, MAURO · 2010 to 2014
$12.4M
TRANS-NETWORK PROJECTSU54CA143837 · NCI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI FERRARI, MAURO · 2009 to 2014
$10.8M
NCI NIH HHS U54 CA143837NCI NIH HHS U54CA143837NCI NIH HHS U54 CA151668NCI NIH HHS U54CA151668
6 · The paper itself

Abstract

We report cell mechanical changes in response to alteration of expression of the human equilibrative nucleoside transporter-1 (hENT1), a most abundant and widely distributed plasma membrane nucleoside transporter in human cells and/or tissues. Modulation of hENT1 expression level altered the stiffness of pancreatic cancer Capan-1 and Panc 03.27 cells, which was analyzed by atomic force microscopy (AFM) and correlated to microfluidic platform. The hENT1 knockdown induced reduction of cellular stiffness in both of cells up to 70%. In addition, cellular phenotypic changes such as cell morphology, migration, and expression level of epithelial-mesenchymal transition (EMT) markers were observed after hENT1 knockdown. Cells with suppressed hENT1 became elongated, migrated faster, and had reduced E-cadherin and elevated N-cadherin compared to parental cells which are consistent with epithelial-mesenchymal transition (EMT). Those cellular phenotypic changes closely correlated with changes in cellular stiffness. This study suggests that hENT1 expression level affects cellular phenotype and cell elastic behavior can be a physical biomarker for quantify hENT1 expression and detect phenotypic shift. Furthermore, cell mechanics can be a critical tool in detecting disease progression and response to therapy.

Indexed as

CadherinsCell Line, TumorCell MovementCell SeparationCell SizeEpithelial-Mesenchymal TransitionEquilibrative Nucleoside Transporter 1Gene Knockdown TechniquesHumansMicrofluidic Analytical TechniquesMicroscopy, Atomic ForcePancreatic NeoplasmsRNA InterferenceRNA, Small InterferingCadherinsEquilibrative Nucleoside Transporter 1RNA, Small InterferingSLC29A1 protein, human

Identifiers

PMID25314577
PMCPMC4196761
OpenAlexW2117364137

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.