Evidence map›Paper›PMID 25866290›Full record

ArticleScientific reports2015

A novel 96well-formatted micro-gap plate enabling drug response profiling on primary tumour samples.

Wei-Yuan Ma, Lo-Chang Hsiung, Chen-Ho Wang, Chi-Ling Chiang, Ching-Hung Lin, Chiun-Sheng Huang, Andrew M Wo

Abstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Review
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  7. Review
  8. Applicability of drug response metrics for cancer studies using biomaterials.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2019
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Three-DimensionalFrontiers in pharmacology · 2018
    Review
  14. 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

7 authors.

Wei-Yuan MaInstitute of Applied Mechanics, National Taiwan University, Taipei, Taiwan.
Lo-Chang HsiungInstitute of Applied Mechanics, National Taiwan University, Taipei, Taiwan.
Chen-Ho WangInstitute of Applied Mechanics, National Taiwan University, Taipei, Taiwan.
Chi-Ling ChiangInstitute of Zoology, National Taiwan University, Taipei, Taiwan.
Ching-Hung LinDepartment of Oncology, National Taiwan University Hospital, Taipei, Taiwan.
Chiun-Sheng HuangDepartment of Surgery, National Taiwan University Hospital, Taipei, Taiwan.
Andrew M WoInstitute of Applied Mechanics, National Taiwan University, Taipei, Taiwan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Drug-based treatments are the most widely used interventions for cancer management. Personalized drug response profiling remains inherently challenging with low cell count harvested from tumour sample. We present a 96well-formatted microfluidic plate with built-in micro-gap that preserves up to 99.2% of cells during multiple assay/wash operation and only 9,000 cells needed for a single reagent test (i.e. 1,000 cells per test spot x 3 selected concentration x triplication), enabling drug screening and compatibility with conventional automated workstations. Results with MCF7 and MDA-MB-231 cell lines showed that no statistical significance was found in dose-response between the device and conventional 96-well plate control. Primary tumour samples from breast cancer patients tested in the device also showed good IC50 prediction. With drug screening of primary cancer cells must consider a wide range of scenarios, e.g. suspended/attached cell types and rare/abundant cell availability, the device enables high throughput screening even for suspended cells with low cell count since the signature microfluidic cell-trapping feature ensures cell preservation in a multiple solution exchange protocol.

Indexed as

Drug Resistance, NeoplasmAgedAntineoplastic AgentsBreast NeoplasmsCell Line, TumorDose-Response Relationship, DrugDrug Evaluation, PreclinicalFemaleHumansIn Vitro TechniquesMiddle AgedNeoplasmsAntineoplastic Agents

Identifiers

PMID25866290
PMCPMC4394194

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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.