Evidence map›Paper›PMID 28667313›Full record

ArticleScientific reports2017

Nanoparticles for live cell microscopy: A surface-enhanced Raman scattering perspective.

Maria Navas-Moreno, Majid Mehrpouyan, Tatyana Chernenko, Demet Candas, Ming Fan, Jian Jian Li, Ming Yan, James W Chan

Open access · goldAbstract 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 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

14 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Review
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  5. Article
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  7. Nanoneedle-Based Materials for Intracellular Studies.Advances in experimental medicine and biology · 2021
    Article
  8. Review
  9. Article
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  11. Article
  12. Review
  13. Review
  14. Comparison of Gold Nanoparticle and Fluorophore-conjugated Antibodies for Labeling Epitopes in Permeabilized Cells.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society
    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

8 authors at 2 institutions in 1 country.

Maria Navas-MorenoUniversity of California-Davis, Center for Biophotonics, Sacramento, 95817, USA.
Majid MehrpouyanBD Biosciences, San Jose, 95131, USA.
Tatyana ChernenkoBD Biosciences, San Jose, 95131, USA.
Demet CandasUniversity of California-Davis, Dept. of Radiation Oncology, Sacramento, 95817, USA.
Ming FanUniversity of California-Davis, Dept. of Radiation Oncology, Sacramento, 95817, USA.
Jian Jian LiUniversity of California-Davis, Dept. of Radiation Oncology, Sacramento, 95817, USA.
Ming YanBD Biosciences, San Jose, 95131, USA.
James W ChanUniversity of California-Davis, Center for Biophotonics, Sacramento, 95817, USA. jwjchan@ucdavis.edu.
University of California, Davis · USBD Biosciences (United States) · US

Funding

Target MKP-1 for Therapy-Resistant Breast Cancer Stem CellsR01CA152313 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LI, JIAN JIAN · 2011 to 2015
$1.9M
NCI NIH HHS R01 CA152313
6 · The paper itself

Abstract

Surface enhanced Raman scattering (SERS) nanoparticles are an attractive alternative to fluorescent probes for biological labeling because of their photostability and multiplexing capabilities. However, nanoparticle size, shape, and surface properties are known to affect nanoparticle-cell interactions. Other issues such as the formation of a protein corona and antibody multivalency interfere with the labeling properties of nanoparticle-antibody conjugates. Hence, it is important to consider these aspects in order to validate such conjugates for live cell imaging applications. Using SERS nanoparticles that target HER2 and CD44 in breast cancer cells, we demonstrate labeling of fixed cells with high specificity that correlates well with fluorescent labels. However, when labeling live cells to monitor surface biomarker expression and dynamics, the nanoparticles are rapidly uptaken by the cells and become compartmentalized into different cellular regions. This behavior is in stark contrast to that of fluorescent antibody conjugates. This study highlights the impact of nanoparticle internalization and trafficking on the ability to use SERS nanoparticle-antibody conjugates to monitor cell dynamics.

Indexed as

MicroscopyNanoparticlesSpectrum Analysis, RamanBiomarkersCell Line, TumorErb-b2 Receptor Tyrosine KinasesFlow CytometryFluorescent Antibody TechniqueFluorescent DyesHumansHyaluronan ReceptorsMolecular ImagingBiomarkersERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesFluorescent DyesHyaluronan Receptors

Identifiers

PMID28667313
PMCPMC5493633
OpenAlexW2722319053

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.