Evidence map›Paper›PMID 27380815›Full record

ArticleNanoscale2016

Designing a multicolor long range nanoscopic ruler for the imaging of heterogeneous tumor cells.

Suhash Reddy Chavva, Bhanu Priya Viraka Nellore, Avijit Pramanik, Sudarson Sekhar Sinha, Stacy Jones, Paresh Chandra Ray

Abstract read
In one paragraph

Article in Nanoscale, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

6 authors.

Suhash Reddy ChavvaDepartment of Chemistry and Biochemistry, Jackson State University, Jackson, MS, USA. paresh.c.ray@jsums.edu.
Bhanu Priya Viraka NelloreDepartment of Chemistry and Biochemistry, Jackson State University, Jackson, MS, USA. paresh.c.ray@jsums.edu.
Avijit PramanikDepartment of Chemistry and Biochemistry, Jackson State University, Jackson, MS, USA. paresh.c.ray@jsums.edu.
Sudarson Sekhar SinhaDepartment of Chemistry and Biochemistry, Jackson State University, Jackson, MS, USA. paresh.c.ray@jsums.edu.
Stacy JonesDepartment of Chemistry and Biochemistry, Jackson State University, Jackson, MS, USA. paresh.c.ray@jsums.edu.
Paresh Chandra RayDepartment of Chemistry and Biochemistry, Jackson State University, Jackson, MS, USA. paresh.c.ray@jsums.edu.

Funding

TRANSCRIPTOMICS OF GIARDIA LAMBLIAG12RR013459 · NCRR · JACKSON STATE UNIVERSITY · PI GAO, RUOMEI · 1998 to 2011
$18.0M
RCMI-Center for Environmental HealthG12MD007581 · NIMHD · JACKSON STATE UNIVERSITY · PI TCHOUNWOU, PAUL B. · 2012 to 2017
$11.2M
NCRR NIH HHS G12 RR013459NIMHD NIH HHS G12 MD007581
6 · The paper itself

Abstract

Tumor heterogeneity is one of the biggest challenges in cancer treatment and diagnosis. A multicolor optical ruler is essential to address the heterogeneous tumor cell complexity. Driven by this need, the current article reports the design of a multicolor long range nanoscopic ruler for screening tumor heterogeneity by accurately identifying epithelial cells and cancer stem cells (CSCs) simultaneously. A nanoscopic surface energy transfer (NSET) ruler has been developed using blue fluorescence polymer dots (PDs) and red fluorescence gold cluster dots (GCDs) as multicolor fluorescence donor and plasmonic gold nanoparticle (GNP) acts as an excellent acceptor. Reported experimental results demonstrated that the multicolor nanoscopic ruler's working window is above 35 nm distances, which is more than three times farther than that of Förster resonance energy transfer (FRET) distance limit. Theoretical modeling using Förster dipole-dipole coupling and dipole to nanoparticle surface energy transfer have been used to discuss the possible mechanism for multicolor nanoscopic ruler's long-range capability. Using RNA aptamers that are specific for the target cancer cells, experimental data demonstrate that the nanoscopic ruler can be used for screening epithelial and CSCs simultaneously from a whole blood sample with a detection capability of 10 cells per mL. Experimental data show that the nanoscopic ruler can distinguish targeted cells from non-targeted cells.

Indexed as

Metal NanoparticlesNeoplastic Cells, CirculatingAptamers, NucleotideFluorescence Resonance Energy TransferFluorescent DyesGlucose-6-Phosphate IsomeraseGoldHumansNeoplastic Stem CellsAptamers, NucleotideFluorescent DyesGlucose-6-Phosphate IsomeraseGold

Identifiers

PMID27380815
PMCPMC4945410

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Registered trials

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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.