Evidence map›Paper›PMID 33722692›Full record

ArticleNanomedicine : nanotechnology, biology, and medicine2021

Preferential uptake of antibody targeted calcium phosphosilicate nanoparticles by metastatic triple negative breast cancer cells in co-cultures of human metastatic breast cancer cells plus bone osteoblasts.

Karen M Bussard, Christopher M Gigliotti, Bernadette M Adair, Jenna M Snyder, Nicholas T Gigliotti, Welley S Loc, Zachary R Wilczynski, Zi-Kui Liu, Kacey Meisel, Cecilia Zemanek and 5 more

Open access · greenAbstract read
In one paragraph

Article in Nanomedicine : nanotechnology, biology, and medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
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  5. Review
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

15 authors at 2 institutions in 1 country.

Karen M BussardDepartment of Cancer Biology, Thomas Jefferson University, Philadelphia, PA.
Christopher M GigliottiDepartment of Bioengineering, The Pennsylvania State University, University Park, PA.
Bernadette M AdairDepartment of Materials Science and Engineering, The Pennsylvania State University, University Park, PA.
Jenna M SnyderDepartment of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, PA.
Nicholas T GigliottiDepartment of Materials Science and Engineering, The Pennsylvania State University, University Park, PA.
Welley S LocDepartment of Chemistry, The Pennsylvania State University, University Park, PA.
Zachary R WilczynskiDepartment of Bioengineering, The Pennsylvania State University, University Park, PA.
Zi-Kui LiuDepartment of Materials Science and Engineering, The Pennsylvania State University, University Park, PA.
Kacey MeiselDepartment of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, PA.
Cecilia ZemanekDepartment of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, PA.
Andrea M MastroDepartment of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, PA.
Alison B ShuppDepartment of Cancer Biology, Thomas Jefferson University, Philadelphia, PA.
Christopher McGovernDepartment of Biochemistry and Molecular Biology, Penn State University College of Medicine, Hershey, PA.
Gail L MattersDepartment of Biochemistry and Molecular Biology, Penn State University College of Medicine, Hershey, PA.
James H AdairDepartment of Bioengineering, The Pennsylvania State University, University Park, PA; Department of Materials Science and Engineering, The Pennsylvania State University, University Park, PA; Department of Pharmacology, Penn State University College of Medicine, Hershey, PA. Electronic address: jha3@ems.psu.edu.
Pennsylvania State University · USThomas Jefferson University · US

Funding

Penn State Clinical and Translational Science InstituteUL1TR000127 · NCATS · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI SINOWAY, LAWRENCE I · 2012 to 2015
$17.1M
Ceraxa (Ceramide NanoLiposome) and Vinblastine For the Improved Treatment of Relapsed or Refractory Acute Myeloid LeukemiaR44CA275609 · NCI · KEYSTONE NANO, INC. · PI ADAIR, BERNADETTE MCMAHON · 2022 to 2023
$2.0M
Novel Nanoparticle Therapy for Pancreatic CancerR01CA167535 · NCI · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI KESTER, MARK, MATTERS, GAIL L. · 2013 to 2017
$1.6M
Breast Cancer Cell Dormancy is Orchestrated by Stroma & Tissue MicroenvironmentR00CA178177 · NCI · THOMAS JEFFERSON UNIVERSITY · PI BUSSARD, KAREN MARIE · 2016 to 2018
$722k
Penn State Clinical and Translational Science InstituteTL1TR000125 · NCATS · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI SINOWAY, LAWRENCE I · 2012 to 2015
$550k
Targeting Pancreatic Cancer with Aptamers to the CCK-B ReceptorR21CA170121 · NCI · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI MATTERS, GAIL L. · 2013 to 2014
$361k
Breast Cancer Cell Dormancy is Orchestrated by Stroma & Tissue MicroenvironmentK99CA178177 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI BUSSARD, KAREN MARIE · 2013 to 2014
$188k
NCATS NIH HHS TL1 TR000125NCATS NIH HHS UL1 TR000127NCI NIH HHS K99 CA178177NCI NIH HHS R00 CA178177NCI NIH HHS R01 CA167535NCI NIH HHS R21 CA170121NCI NIH HHS R44 CA275609
6 · The paper itself

Abstract

Calcium phosphosilicate nanoparticles (CPSNPs) are bioresorbable nanoparticles that can be bioconjugated with targeting molecules and encapsulate active agents and deliver them to tumor cells without causing damage to adjacent healthy tissue. Data obtained in this study demonstrated that an anti-CD71 antibody on CPSNPs targets these nanoparticles and enhances their internalization by triple negative breast cancer cells in-vitro. Caspase 3,7 activation, DNA damage, and fluorescent microscopy confirmed the apoptotic breast cancer response caused by targeted anti-CD71-CPSNPs encapsulated with gemcitabine monophosphate, the active metabolite of the chemotherapeutic gemcitabine used to treat cancers including breast and ovarian. Targeted anti-CD71-CPSNPs encapsulated with the fluorophore, Rhodamine WT, were preferentially internalized by breast cancer cells in co-cultures with osteoblasts. While osteoblasts partially internalized anti-CD71-GemMP-CPSNPs, their cell growth was not affected. These results suggest that CPSNPs may be used as imaging tools and selective drug delivery systems for breast cancer that has metastasized to bone.

Indexed as

NanoparticlesNeoplasm Metastasis3T3 CellsAnimalsAntibodiesCalcium CompoundsCoculture TechniquesFemaleHumansMiceOsteoblastsSilicatesTriple Negative Breast NeoplasmsAntibodiesCalcium Compoundscalcium silicateSilicatesBoneGemcitabineMetastatic breast cancerNanodeliveryNanoparticleOsteoblast

Identifiers

PMID33722692
PMCPMC8627646
OpenAlexW3136033923

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.