Evidence map›Paper›PMID 23369215›Full record

ArticleBiomaterials2013

Pegylated siRNA-loaded calcium phosphate nanoparticle-driven amplification of cancer cell internalization in vivo.

Lisa A Tobin, Yili Xie, Maria Tsokos, Su I Chung, Allison A Merz, Michael A Arnold, Guang Li, Harry L Malech, King F Kwong

Open access · greenAbstract read
In one paragraph

Article in Biomaterials, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.2field-weighted citation impact, top 14% 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

12 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Biological and Medical Applications of Calcium Phosphate Nanoparticles.Chemistry (Weinheim an der Bergstrasse, Germany) · 2021
    Review
  5. Biodegradable calcium phosphate nanoparticles for cancer therapy.Advances in colloid and interface science · 2020
    Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. 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

9 authors at 3 institutions in 1 country.

Lisa A TobinThoracic Oncology Section, Surgery Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892-1201, USA.
Yili Xie
Maria Tsokos
Su I Chung
Allison A Merz
Michael A Arnold
Guang Li
Harry L Malech
King F Kwong
National Institutes of Health · USNational Cancer Institute · USBeth Israel Deaconess Medical Center · US

Funding

Gene Therapy Basic Research to Treat Inherited Primary Immune DeficienciesZIAAI000644 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI MALECH, HARRY L · 2009 to 2025
$12.1M
Basic Research on Hematopoietic Human Stem CellsZIAAI000988 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI MALECH, HARRY L · 2009 to 2019
$6.5M
Development and evaluation of apoptosis targeted therapies in lung cancerZIABC011049 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI KWONG, KING · 2009 to 2013
$1.7M
Mechanisms of apoptosis regulation which impede cancer cell death in lung cancerZIABC011046 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI KWONG, KING · 2009 to 2013
$1.6M
Intramural NIH HHS Z99 CA999999Intramural NIH HHS ZIA BC011046Intramural NIH HHS ZIA BC011049NCI NIH HHS Y99 CA999999
6 · The paper itself

Abstract

The cell membrane is a critical barrier to effective delivery for many therapeutics, including those which are nanoparticle-based. Improving nanoparticle transport across the cell membrane remains a fundamental challenge. Cancer cells preferentially internalized pegylated calcium phosphate nanoparticles over normal epithelial cells. Furthermore, non-cytotoxic levels of doxorubicin markedly amplified this difference by increasing free unbound caveolin-1 and resulted in enhanced caveolin-mediated nanoparticle endocytosis in cancer cells. Engineered pegylated siRNA-loaded triple-shell calcium phosphate nanoconstructs incorporating ultra-low levels of doxorubicin recapitulated these effects and delivered increased numbers of siRNA into cancer cells with target-specific results. Systemic administration of nanoparticles in vivo demonstrated highly preferential entry into tumors, little bystander organ biodistribution, and significant tumor growth arrest. In conclusion, siRNA-loaded calcium phosphate nanoparticles incorporating non-cytotoxic amounts of doxorubicin markedly enhances nanoparticle internalization and results in increased payload delivery with concomitant on-target effects.

Indexed as

EndocytosisNanoparticlesBase SequenceCalcium PhosphatesCell Line, TumorCells, CulturedDNA PrimersDoxorubicinHumansMicroscopy, ConfocalMicroscopy, ElectronNeoplasmsPolyethylene GlycolsReactive Oxygen SpeciesReal-Time Polymerase Chain ReactionRNA, Small InterferingCalcium PhosphatesDNA PrimersDoxorubicinPolyethylene GlycolsReactive Oxygen SpeciesRNA, Small Interfering

Identifiers

PMID23369215
PMCPMC3633203
OpenAlexW2063426506

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.