Evidence map›Paper›PMID 31259527›Full record

ArticleACS nano2019

Spatiotemporal Tracking of Brain-Tumor-Associated Myeloid Cells

Elliott Daniel SoRelle, Derek William Yecies, Orly Liba, Frederick Christian Bennett, Claus Moritz Graef, Rebecca Dutta, Siddhartha Mitra, Lydia-Marie Joubert, Samuel Cheshier, Gerald A Grant and 1 more

Open access · greenAbstract read
In one paragraph

Article in ACS nano, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

11 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Spatiotemporal tracking of gold nanorods after intranasal administration for brain targeting.Journal of controlled release : official journal of the Controlled Release Society · 2023
    Article
  5. Biomedical optics express · 2022
    Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. 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

11 authors at 3 institutions in 1 country.

Elliott Daniel SoRelleORCID 0000-0002-3362-1028
Derek William Yecies
Frederick Christian Bennett
Claus Moritz Graef
Siddhartha Mitra
Lydia-Marie Joubert
Samuel Cheshier
Gerald A Grant
Adam de la ZerdaThe Chan Zuckerberg Biohub , 499 Illinois Street , San Francisco , California 94158 , United States.
Stanford University · USCalifornia Institute for Regenerative Medicine · USChan Zuckerberg Initiative (United States) · US

Funding

Pilot ProjectsU54CA151459 · NCI · STANFORD UNIVERSITY · PI GAMBHIR, SANJIV S · 2010 to 2014
$12.6M
Molecular Biophysics Training Program at StanfordT32GM008294 · NIGMS · STANFORD UNIVERSITY · PI HUANG, KERWYN C. · 1989 to 2019
$7.4M
VECTOR COREP30NS069375 · NINDS · STANFORD UNIVERSITY · PI STEINBERG, GARY K · 2011 to 2019
$6.3M
Stanford Neurosurgery Resident Research Education ProgramR25NS065741 · NINDS · STANFORD UNIVERSITY · PI HAYDEN GEPHART, MELANIE, PORTER, BRENDA ELAINE · 2009 to 2022
$2.0M
Molecular Imaging of Protein Glycosylation in Living SubjectsDP5OD012179 · OD · STANFORD UNIVERSITY · PI DE LA ZERDA, ADAM · 2012 to 2016
$2.0M
NCI NIH HHS U54 CA151459NIGMS NIH HHS T32 GM008294NIH HHS DP5 OD012179NINDS NIH HHS P30 NS069375NINDS NIH HHS R25 NS065741
6 · The paper itself

Abstract

By their nature, tumors pose a set of profound challenges to the immune system with respect to cellular recognition and response coordination. Recent research indicates that leukocyte subpopulations, especially tumor-associated macrophages (TAMs), can exert substantial influence on the efficacy of various cancer immunotherapy treatment strategies. To better study and understand the roles of TAMs in determining immunotherapeutic outcomes, significant technical challenges associated with dynamically monitoring single cells of interest in relevant live animal models of solid tumors must be overcome. However, imaging techniques with the requisite combination of spatiotemporal resolution, cell-specific contrast, and sufficient signal-to-noise at increasing depths in tissue are exceedingly limited. Here we describe a method to enable high-resolution, wide-field, longitudinal imaging of TAMs based on speckle-modulating optical coherence tomography (SM-OCT) and spectral scattering from an optimized contrast agent. The approach's improvements to OCT detection sensitivity and noise reduction enabled high-resolution OCT-based observation of individual cells of a specific host lineage in live animals. We found that large gold nanorods (LGNRs) that exhibit a narrow-band, enhanced scattering cross-section can selectively label TAMs and activate microglia in an

Indexed as

Cell TrackingImaging, Three-DimensionalTomography, Optical CoherenceAnimalsBrain NeoplasmsCell Line, TumorContrast MediaDisease Models, AnimalFemaleHumansMiceMice, NudeMyeloid CellsNeoplasms, ExperimentalParticle SizeSurface PropertiesContrast Mediabiomedical imagingglioblastomagold nanorodsOCTtumor-associated macrophages

Identifiers

PMID31259527
PMCPMC8144904
OpenAlexW2954889534

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.