Evidence map›Paper›PMID 34308266›Full record

ArticleACS applied nano materials2019

Surface-Enhanced Raman Spectroscopy Characterization of Breast Cell Phenotypes: Effect of Nanoparticle Geometry.

Richard E Darienzo, Jingming Wang, Olivia Chen, Maurinne Sullivan, Tatsiana Mironava, Hyungjin Kim, Rina Tannenbaum

Abstract read
In one paragraph

Article in ACS applied nano materials, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. 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.

Richard E DarienzoDepartment of Materials Science and Chemical Engineering, Stony Brook University, Stony Brook, New York 11794, United States.ORCID 0000-0003-0908-5197
Jingming WangDepartment of Pharmacological Sciences, Stony Brook University, Stony Brook, 11794, United States.
Olivia ChenDepartment of Materials Science and Chemical Engineering, Stony Brook University, Stony Brook, New York 11794, United States.
Maurinne SullivanDepartment of Chemistry, Stony Brook University, Stony Brook, New York 11794, United States.
Tatsiana MironavaDepartment of Materials Science and Chemical Engineering, Stony Brook University, Stony Brook, New York 11794, United States.
Hyungjin KimDepartment of Pharmacological Sciences, Stony Brook University, Stony Brook, 11794, United States.
Rina TannenbaumDepartment of Materials Science and Chemical Engineering, Stony Brook University, Stony Brook, New York 11794, United States.ORCID 0000-0001-9389-045X

Funding

Proteolytic control of DNA interstrand cross-link repair and genome integrityR01CA218132 · NCI · STATE UNIVERSITY NEW YORK STONY BROOK · PI KIM, HYUNGJIN · 2018 to 2022
$1.8M
Scholars in BioMedical Sciences (SBMS) Training ProgramT32GM127253 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI TSIRKA, STYLIANI-ANNA (STELLA) E · 2018 to 2022
$689k
NCI NIH HHS R01 CA218132NIGMS NIH HHS T32 GM127253
6 · The paper itself

Abstract

The use of surface-enhanced Raman spectroscopy (SERS) to delineate between the breast epithelial cell lines MCF10A, SK-BR-3, and MDA-MB-231 is explored utilizing varied morphologies of gold nanoparticles. The nanoparticles studied had spherical, star-like, and quasi-fractal (nanocaltrop) morphologies and possessed varying degrees of surface inhomogeneity and complexity. The efficacy of Raman enhancement of these nanoparticles was a function of their size, their surface morphology, and the associated density of "hot spots," as well as their cellular uptake. The spherical and star-like nanoparticles provided strong signal enhancement that allowed for the discernment among the three cell phenotypes based solely on the acquired Raman spectra. The presence of overlapping Raman band spectral regions, as well as unique spectral bands, suggests that the underlying biological differences between these cells can be accessed without the need for tagging the nanoparticles or for specific cell targeting, demonstrating the potential ubiquity of this technique in imaging any cancer. This work provides clear evidence for the potential application of SERS as a tool for mapping cancerous lesions, possibly during surgery and under histopathological analysis.

Indexed as

breast cancergold nanoparticlesHER2 amplificationnanoscale synthesisRaman spectroscopysurface interactionssurface plasmon

Identifiers

PMID34308266
PMCPMC8297918

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.