Evidence map›Paper›PMID 23345442›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2013

Biomimetic, synthetic HDL nanostructures for lymphoma.

Shuo Yang, Marina G Damiano, Heng Zhang, Sushant Tripathy, Andrea J Luthi, Jonathan S Rink, Andrey V Ugolkov, Amareshwar T K Singh, Sandeep S Dave, Leo I Gordon and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

78 citing papers in PubMed, 127 citations in OpenAlex.

  1. Article
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  5. Article
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  8. Unlocking Transplant Tolerance with Biomaterials.Advanced healthcare materials · 2025
    Review
  9. Article
  10. Article
  11. Article
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  13. Article
  14. Review
  15. Review
  16. Nanomedicine in cancer therapy.Signal transduction and targeted therapy · 2023
    Review
  17. Review
  18. Article
  19. Article
  20. Review

18 more citing papers are in PubMed but not listed here.

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 2 institutions in 1 country.

Shuo YangDepartment of Medicine, Division of Hematology/Oncology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.
Marina G Damiano
Heng Zhang
Sushant Tripathy
Andrea J Luthi
Jonathan S Rink
Andrey V Ugolkov
Amareshwar T K Singh
Sandeep S Dave
Leo I Gordon
C Shad Thaxton
Northwestern University · USDuke University · US

Funding

Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Daniela E Matei · 1993 to 2026
$153.9M
Theranostic Magnetic Nanostructures for the Molecular Imaging of CancerU54CA151880 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI MIRKIN, CHAD A. · 2010 to 2014
$11.5M
Howard Hughes Medical InstituteNCI NIH HHS P30 CA060553NCI NIH HHS U54 CA151880
6 · The paper itself

Abstract

New therapies that challenge existing paradigms are needed for the treatment of cancer. We report a nanoparticle-enabled therapeutic approach to B-cell lymphoma using synthetic high density lipoprotein nanoparticles (HDL-NPs). HDL-NPs are synthesized using a gold nanoparticle template to control conjugate size and ensure a spherical shape. Like natural HDLs, biomimetic HDL-NPs target scavenger receptor type B-1, a high-affinity HDL receptor expressed by lymphoma cells. Functionally, compared with natural HDL, the gold NP template enables differential manipulation of cellular cholesterol flux in lymphoma cells, promoting cellular cholesterol efflux and limiting cholesterol delivery. This combination of scavenger receptor type B-1 binding and relative cholesterol starvation selectively induces apoptosis. HDL-NP treatment of mice bearing B-cell lymphoma xenografts selectively inhibits B-cell lymphoma growth. As such, HDL-NPs are biofunctional therapeutic agents, whose mechanism of action is enabled by the presence of a synthetic nanotemplate. HDL-NPs are active in B-cell lymphomas and potentially, other malignancies or diseases of pathologic cholesterol accumulation.

Indexed as

AnimalsAnnexin A5ApoptosisBiomimeticsBlotting, WesternFluorescein-5-isothiocyanateHumansImmunoblottingJurkat CellsLipoproteins, HDLLymphoma, B-CellMass SpectrometryMetal NanoparticlesMiceMicroscopy, Electron, TransmissionScavenger Receptors, Class BAnnexin A5Fluorescein-5-isothiocyanateLipoproteins, HDLScavenger Receptors, Class B

Identifiers

PMID23345442
PMCPMC3574906
OpenAlexW2051434186

What OpenQuestion holds

Textmetadata
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.