Evidence map›Paper›PMID 25176061›Full record

ArticleBiomaterials2014

Thiol-ene hydrogels as desmoplasia-mimetic matrices for modeling pancreatic cancer cell growth, invasion, and drug resistance.

Chang Seok Ki, Tsai-Yu Lin, Murray Korc, Chien-Chi Lin

Open access · greenAbstract read
In one paragraph

Article in Biomaterials, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

33 citing papers in PubMed, 69 citations in OpenAlex.

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  13. Assessing monocyte phenotype in poly(Biomedical materials (Bristol, England) · 2021
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  18. Engineering of biomaterials for tumor modeling.Materials today. Advances · 2020
    Article
  19. Frontiers in medical technology · 2020
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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 2 institutions in 2 countries.

Chang Seok KiDepartment of Biomedical Engineering, Purdue School of Engineering and Technology, Indianapolis University-Purdue University Indianapolis, Indianapolis, IN 46202, USA; Department of Biosystems and Biomaterials Science and Engineering, Seoul National University, Seoul 151-921, Republic of Korea.
Tsai-Yu LinDepartment of Biomedical Engineering, Purdue School of Engineering and Technology, Indianapolis University-Purdue University Indianapolis, Indianapolis, IN 46202, USA.
Murray KorcDepartment of Medicine and Biochemistry and Molecular Biology, Indiana University School of Medicine, The Melvin and Bren Simon Cancer Center and the Center for Pancreatic Cancer Research, Indianapolis, IN 46202, USA.
Chien-Chi LinDepartment of Biomedical Engineering, Purdue School of Engineering and Technology, Indianapolis University-Purdue University Indianapolis, Indianapolis, IN 46202, USA. Electronic address: lincc@iupui.edu.
University of Indianapolis · USIndiana University Health · US

Funding

Novel aspects of Epithelial-Mesenchymal Transition(EMT)in pancreatic cancerR01CA075059 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI KORC, MURRAY · 1997 to 2018
$4.3M
Thiol-Ene Click Hydrogels for in situ Cell Expansion and DifferentiationR21EB013717 · NIBIB · INDIANA UNIVERSITY INDIANAPOLIS · PI LIN, CHIEN-CHI · 2011 to 2012
$407k
NCI NIH HHS R01 CA075059NIBIB NIH HHS R21 EB013717NIBIB NIH HHS R21EB013717
6 · The paper itself

Abstract

The development of pancreatic ductal adenocarcinoma (PDAC) is heavily influenced by local stromal tissues, or desmoplasia. Biomimetic hydrogels capable of mimicking tumor niches are particularly useful for discovering the role of independent matrix cues on cancer cell development. Here, we report a photo-curable and bio-orthogonal thiol-ene (i.e., cross-linked by mutually reactive norbornene and thiol groups via photoinitiation) hydrogel platform for studying the growth, morphogenesis, drug resistance, and cancer stem cell marker expression in PDAC cells cultured in 3D. The hydrogels were prepared from multi-arm poly(ethylene glycol)-norbornene cross-linked with protease-sensitive peptide to permit cell-mediated matrix remodeling. Collagen 1 fibrils were incorporated into the covalent network while cytokines (e.g., EGF and TGF-β1) were supplemented in the culture media for controlling cell fate. We found that the presence of collagen 1 enhanced cell proliferation and Yes-associated protein (YAP) translocation to cell nuclei. Cytokines and collagen 1 synergistically up-regulated MT1-MMP expression and induced cell spreading, suggestive of epithelial-mesenchymal transition (EMT) in the encapsulated cells. Furthermore, PDAC cells cultured in 3D developed chemo-resistance even in the absence of collagen 1 and cytokines. This phenotype is likely a consequence of the enrichment of pancreatic cancer stem cells that expressed high levels of CD24, sonic hedgehog (SHH), and vascular endothelial growth factor (VEGF).

Indexed as

AdenocarcinomaBiomimetic MaterialsCarcinoma, Pancreatic DuctalCell Culture TechniquesCell Line, TumorCell ProliferationDrug Resistance, NeoplasmEpithelial-Mesenchymal TransitionHumansHydrogelsNeoplasm InvasivenessPancreasPancreatic NeoplasmsSulfhydryl CompoundsHydrogelsSulfhydryl CompoundsChemo-resistanceEpithelial-mesenchymal transitionHydrogelPancreatic cancer stem cellPancreatic ductal adenocarcinoma

Identifiers

PMID25176061
PMCPMC4164606
OpenAlexW1989727548

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.