Evidence map›Paper›PMID 27581736›Full record

ArticleScientific reports2016

Stand-Sit Microchip for High-Throughput, Multiplexed Analysis of Single Cancer Cells.

Lisa Ramirez, Jason I Herschkowitz, Jun Wang

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.4field-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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. The Intriguing Landscape of Single-Cell Protein Analysis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2022
    Review
  2. Single-Cell Proteomics.Trends in biochemical sciences · 2021
    Review
  3. Article
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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

3 authors at 2 institutions in 1 country.

Lisa RamirezMultiplex Biotechnology Laboratory, Department of Chemistry, University at Albany, State University of New York, Albany, NY 12222, USA.
Jason I HerschkowitzCancer Research Center, University at Albany, State University of New York, Rensselaer, NY 12144, USA.
Jun WangMultiplex Biotechnology Laboratory, Department of Chemistry, University at Albany, State University of New York, Albany, NY 12222, USA.
University at Albany, State University of New York · USAlbany State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cellular heterogeneity in function and response to therapeutics has been a major challenge in cancer treatment. The complex nature of tumor systems calls for the development of advanced multiplexed single-cell tools that can address the heterogeneity issue. However, to date such tools are only available in a laboratory setting and don't have the portability to meet the needs in point-of-care cancer diagnostics. Towards that application, we have developed a portable single-cell system that is comprised of a microchip and an adjustable clamp, so on-chip operation only needs pipetting and adjusting of clamping force. Up to 10 proteins can be quantitated from each cell with hundreds of single-cell assays performed in parallel from one chip operation. We validated the technology and analyzed the oncogenic signatures of cancer stem cells by quantitating both aldehyde dehydrogenase (ALDH) activities and 5 signaling proteins in single MDA-MB-231 breast cancer cells. The technology has also been used to investigate the PI3K pathway activities of brain cancer cells expressing mutant epidermal growth factor receptor (EGFR) after drug intervention targeting EGFR signaling. Our portable single-cell system will potentially have broad application in the preclinical and clinical settings for cancer diagnosis in the future.

Indexed as

Gene Expression Regulation, NeoplasticLab-On-A-Chip DevicesAldehyde DehydrogenaseBrain NeoplasmsBreast NeoplasmsCell Line, TumorErbB ReceptorsHigh-Throughput Screening AssaysHumansIntracellular Signaling Peptides and ProteinsNeoplasm ProteinsNeoplastic Stem CellsPhosphatidylinositol 3-KinasesPoint-of-Care SystemsSignal TransductionSingle-Cell AnalysisAldehyde DehydrogenaseEGFR protein, humanErbB ReceptorsIntracellular Signaling Peptides and ProteinsNeoplasm ProteinsPhosphatidylinositol 3-Kinases

Identifiers

PMID27581736
PMCPMC5007481
OpenAlexW2517777130

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.