Evidence map›Paper›PMID 28240272›Full record

ArticleScientific reports2017

A Microfabricated 96-Well 3D Assay Enabling High-Throughput Quantification of Cellular Invasion Capabilities.

Rui Hao, Yuanchen Wei, Chaobo Li, Feng Chen, Deyong Chen, Xiaoting Zhao, Shaoliang Luan, Beiyuan Fan, Wei Guo, Junbo Wang and 1 more

Abstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

11 authors.

Rui HaoState Key Laboratory of Transducer Technology, Institute of Electronics, Chinese Academy of Sciences, Beijing 100190, P.R. China.
Yuanchen WeiState Key Laboratory of Transducer Technology, Institute of Electronics, Chinese Academy of Sciences, Beijing 100190, P.R. China.
Chaobo LiMicroelectronics Equipment Research and Development Center, Institute of Microelectronics of Chinese Academy of Sciences, Beijing 100029, P.R. China.
Feng ChenDepartment of Vascular Surgery, Clinical Division of Surgery, Chinese PLA General Hospital, Beijing 100853, P.R. China.
Deyong ChenState Key Laboratory of Transducer Technology, Institute of Electronics, Chinese Academy of Sciences, Beijing 100190, P.R. China.
Xiaoting ZhaoDepartment of Cellular and Molecular Biology, Beijing Chest Hospital, Capital Medical University, Beijing 101149, P.R. China.
Shaoliang LuanDepartment of Vascular Surgery, Clinical Division of Surgery, Chinese PLA General Hospital, Beijing 100853, P.R. China.
Beiyuan FanState Key Laboratory of Transducer Technology, Institute of Electronics, Chinese Academy of Sciences, Beijing 100190, P.R. China.
Wei GuoDepartment of Vascular Surgery, Clinical Division of Surgery, Chinese PLA General Hospital, Beijing 100853, P.R. China.
Junbo WangState Key Laboratory of Transducer Technology, Institute of Electronics, Chinese Academy of Sciences, Beijing 100190, P.R. China.
Jian ChenState Key Laboratory of Transducer Technology, Institute of Electronics, Chinese Academy of Sciences, Beijing 100190, P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This paper presents a 96-well microfabricated assay to study three-dimensional (3D) invasion of tumor cells. A 3D cluster of tumor cells was first generated within each well by seeding cells onto a micro-patterned surface consisting of a central fibronectin-coated area that promotes cellular attachment, surrounded by a poly ethylene glycol (PEG) coated area that is resistant to cellular attachment. Following the formation of the 3D cell clusters, a 3D collagen extracellular matrix was formed in each well by thermal-triggered gelation. Invasion of the tumor cells into the extracellular matrix was subsequently initiated and monitored. Two modes of cellular infiltration were observed: A549 cells invaded into the extracellular matrix following the surfaces previously coated with PEG molecules in a pseudo-2D manner, while H1299 cells invaded into the extracellular matrix in a truly 3D manner including multiple directions. Based on the processing of 2D microscopic images, a key parameter, namely, equivalent invasion distance (the area of invaded cells divided by the circumference of the initial cell cluster) was obtained to quantify migration capabilities of these two cell types. These results validate the feasibility of the proposed platform, which may function as a high-throughput 3D cellular invasion assay.

Indexed as

Biological AssayCell MovementA549 CellsCell Culture TechniquesCell Line, TumorCollagenDiffusion Chambers, CultureDimethylpolysiloxanesExtracellular MatrixFibronectinsHumansMicrotechnologyOrgan SpecificityPolyestersPolyethylene GlycolsbaysilonCollagenDimethylpolysiloxanesFibronectinsFN1 protein, humanPolyestersPolyethylene Glycolspoly(lactide)

Identifiers

PMID28240272
PMCPMC5327465

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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.