Evidence map›Paper›PMID 22928955›Full record

ArticleACS nano2012

Coassembled cytotoxic and pegylated peptide amphiphiles form filamentous nanostructures with potent antitumor activity in models of breast cancer.

Daniel J Toft, Tyson J Moyer, Stephany M Standley, Yves Ruff, Andrey Ugolkov, Samuel I Stupp, Vincent L Cryns

Abstract read
In one paragraph

Article in ACS nano, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing 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

37 citing papers in PubMed.

  1. Article
  2. Article
  3. Peptide-based drugs in immunotherapy: current advances and future prospects.Medical oncology (Northwood, London, England) · 2025
    Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Current Progress in Cross-Linked Peptide Self-Assemblies.International journal of molecular sciences · 2020
    Review
  12. Article
  13. Article
  14. Article
  15. Supramolecular Self-Assembly To Control Structural and Biological Properties of Multicomponent Hydrogels.Chemistry of materials : a publication of the American Chemical Society · 2019
    Article
  16. Article
  17. Article
  18. Multicomponent peptide assemblies.Chemical Society reviews · 2018
    Review
  19. Article
  20. Supramolecular Assembly of Peptide Amphiphiles.Accounts of chemical research · 2017
    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

7 authors.

Daniel J ToftInstitute for BioNanotechnology in Medicine, Northwestern University, Chicago, Illinois 60611, United States.
Tyson J Moyer
Stephany M Standley
Yves Ruff
Andrey Ugolkov
Samuel I Stupp
Vincent L Cryns

Funding

Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Daniela E Matei · 1993 to 2026
$153.9M
TiO2 nanocomposites for Targeted Treatment and Imaging of Prostate cancerU54CA119341 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI STUPP, SAMUEL I · 2005 to 2009
$19.9M
TRAINING IN METABOLISM, DIABETES AND ENDOCRINOLOGYT32DK007169 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Joseph Bass · 1988 to 2026
$6.6M
Tumor Targeted Nanobins for the Treatment of Metastatic Breast and Ovarian CancerU01CA151461 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI O'HALLORAN, THOMAS V · 2010 to 2014
$2.2M
Dendritic Peptide Amphiphiles for Biomedical ApplicationsF32GM080021 · NIGMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI STANDLEY, STEPHANY · 2007 to 2009
$133k
NCI NIH HHS 1U54CA119341NCI NIH HHS NCI CA060553NCI NIH HHS NCI CCSG P30 CA060553NCI NIH HHS P30 CA060553NCI NIH HHS U01 CA151461NCI NIH HHS U54 CA119341NIDDK NIH HHS T32 DK007169NIDDK NIH HHS T32DK007169NIGMS NIH HHS 5F32GM080021NIGMS NIH HHS F32 GM080021
6 · The paper itself

Abstract

Self-assembled peptide amphiphiles (PAs) consisting of hydrophobic, hydvrogen-bonding, and charged hydrophilic domains form cylindrical nanofibers in physiological conditions and allow for the presentation of a high density of bioactive epitopes on the nanofiber surface. We report here on the use of PAs to form multifunctional nanostructures with tumoricidal activity. The combination of a cationic, membrane-lytic PA coassembled with a serum-protective, pegylated PA was shown to self-assemble into nanofibers. Addition of the pegylated PA to the nanostructure substantially limited degradation of the cytolytic PA by the protease trypsin, with an 8-fold increase in the amount of intact PA observed after digestion. At the same time, addition of up to 50% pegylated PA to the nanofibers did not decrease the in vitro cytotoxicity of the cytolytic PA. Using a fluorescent tag covalently attached to PA nanofibers we were able to track the biodistribution in plasma and tissues of tumor-bearing mice over time after intraperitoneal administration of the nanoscale filaments. Using an orthotopic mouse xenograft model of breast cancer, systemic administration of the cytotoxic pegylated nanostructures significantly reduced tumor cell proliferation and overall tumor growth, demonstrating the potential of multifunctional PA nanostructures as versatile cancer therapeutics.

Indexed as

AnimalsAntineoplastic AgentsBreast NeoplasmsCell Line, TumorFemaleHumansMaterials TestingMiceMice, NudeNanostructuresPeptidesPolyethylene GlycolsSurface-Active AgentsTreatment OutcomeAntineoplastic AgentsPeptidesPolyethylene GlycolsSurface-Active Agents

Identifiers

PMID22928955
PMCPMC3458188

What OpenQuestion holds

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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.