Evidence map›Paper›PMID 32462807›Full record

ArticleSmall (Weinheim an der Bergstrasse, Germany)2021

Fluorescent Silica Nanoparticles to Label Metastatic Tumor Cells in Mineralized Bone Microenvironments.

Aaron E Chiou, Joshua A Hinckley, Rupal Khaitan, Neta Varsano, Jonathan Wang, Henry F Malarkey, Christopher J Hernandez, Rebecca M Williams, Lara A Estroff, Steve Weiner and 3 more

Abstract read
In one paragraph

Article in Small (Weinheim an der Bergstrasse, Germany), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Biomaterials for Orthopaedic Diagnostics and Theranostics.Current opinion in biomedical engineering · 2021
    Article
  7. Review
  8. 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

13 authors.

Aaron E ChiouMeinig School of Biomedical Engineering, Cornell University, Ithaca, NY, 14853, USA.ORCID 0000-0002-3762-9385
Joshua A HinckleyDepartment of Chemistry and Chemical Biology, Cornell University, Ithaca, NY, 14853, USA.ORCID 0000-0002-0575-5045
Rupal KhaitanMeinig School of Biomedical Engineering, Cornell University, Ithaca, NY, 14853, USA.
Neta VarsanoDepartment of Structural Biology, Weizmann Institute of Science, Rehovot, 7610001, Israel.
Jonathan WangDivision of Nutritional Sciences, Cornell University, Ithaca, NY, 14853, USA.
Henry F MalarkeyDepartment of Applied and Engineering Physics, Cornell University, Ithaca, NY, 14853, USA.
Christopher J HernandezMeinig School of Biomedical Engineering, Cornell University, Ithaca, NY, 14853, USA.ORCID 0000-0002-0712-6533
Rebecca M WilliamsBiotechnology Resource Center Imaging Facility, Cornell University, Ithaca, NY, 14853, USA.
Lara A EstroffDepartment of Materials Science and Engineering, Cornell University, Ithaca, NY, 14853, USA.ORCID 0000-0002-7658-1265
Steve WeinerDepartment of Structural Biology, Weizmann Institute of Science, Rehovot, 7610001, Israel.
Lia AddadiDepartment of Structural Biology, Weizmann Institute of Science, Rehovot, 7610001, Israel.
Ulrich B WiesnerDepartment of Materials Science and Engineering, Cornell University, Ithaca, NY, 14853, USA.
Claudia FischbachMeinig School of Biomedical Engineering, Cornell University, Ithaca, NY, 14853, USA.ORCID 0000-0002-9368-0150

Funding

Project 3: Physical and Metabolic Constraints of Cancer Cell InvasionU54CA210184 · NCI · CORNELL UNIVERSITY · PI CANTLEY, LEWIS C., FISCHBACH, CLAUDIA · 2016 to 2020
$10.2M
Real-time Intraoperative Imaging of Cancer Biomarkers and Peripheral NervesU54CA199081 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI LEWIS, JASON S. · 2015 to 2019
$8.3M
Broad wavelength range Zeiss 780 NLO/confocal system for the Cornell Imaging CoreS10OD018516 · OD · CORNELL UNIVERSITY · PI ZIPFEL, WARREN R · 2014 to 2014
$834k
In Vivo Optical and MicroCT Imaging Instruments for the Cornell BRC Imaging FacilityS10OD025049 · OD · CORNELL UNIVERSITY · PI WILLIAMS, REBECCA M · 2018 to 2018
$750k
Acquisition of a VisualSonics Vevo 2100 mouse ultrasound for Cornell Imaging faciS10OD016191 · OD · CORNELL UNIVERSITY · PI WILLIAMS, REBECCA M · 2014 to 2014
$534k
Zeiss LSM710 Confocal Microscope for Shared Imaging FacilityS10RR025502 · NCRR · CORNELL UNIVERSITY · PI WILLIAMS, REBECCA M · 2009 to 2009
$500k
The Role of Bone Resorption in Bone Marrow LesionsR21AR073454 · NIAMS · CORNELL UNIVERSITY · PI HERNANDEZ, CHRISTOPHER JOHN · 2018 to 2019
$407k
A Light Sheet Microscope for the Cornell BRC Imaging FacilityS10OD023466 · OD · CORNELL UNIVERSITY · PI WILLIAMS, REBECCA M · 2017 to 2017
$364k
Breast cancer-derived factors and their role in bone pre-metastatic niche formationF31CA228448 · NCI · CORNELL UNIVERSITY · PI CHIOU, AARON · 2018 to 2019
$90k
NCI NIH HHS F31 CA228448NCI NIH HHS U54 CA199081NCI NIH HHS U54 CA210184NCRR NIH HHS S10 RR025502NIAMS NIH HHS R21 AR073454NIH HHS S10 OD016191NIH HHS S10 OD018516NIH HHS S10 OD023466NIH HHS S10 OD025049
6 · The paper itself

Abstract

During breast cancer bone metastasis, tumor cells interact with bone microenvironment components including inorganic minerals. Bone mineralization is a dynamic process and varies spatiotemporally as a function of cancer-promoting conditions such as age and diet. The functional relationship between skeletal dissemination of tumor cells and bone mineralization, however, is unclear. Standard histological analysis of bone metastasis frequently relies on prior demineralization of bone, while methods that maintain mineral are often harsh and damage fluorophores commonly used to label tumor cells. Here, fluorescent silica nanoparticles (SNPs) are introduced as a robust and versatile labeling strategy to analyze tumor cells within mineralized bone. SNP uptake and labeling efficiency of MDA-MB-231 breast cancer cells is characterized with cryo-scanning electron microscopy and different tissue processing methods. Using a 3D in vitro model of marrow-containing, mineralized bone as well as an in vivo model of bone metastasis, SNPs are demonstrated to allow visualization of labeled tumor cells in mineralized bone using various imaging modalities including widefield, confocal, and light sheet microscopy. This work suggests that SNPs are valuable tools to analyze tumor cells within mineralized bone using a broad range of bone processing and imaging techniques with the potential to increase the understanding of bone metastasis.

Indexed as

Bone NeoplasmsBreast NeoplasmsNanoparticlesBone and BonesCell Line, TumorFemaleHumansSilicon DioxideTumor MicroenvironmentSilicon Dioxidebone imagingbone metastasisbone metastasis imagingbone mineralsbreast cancer cell labelingsilica nanoparticles

Identifiers

PMID32462807
PMCPMC7704907

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.