Evidence map›Paper›PMID 34899115›Full record

ArticleAdvanced functional materials2021

Camouflaged Hybrid Cancer Cell-Platelet Fusion Membrane Nanovesicles Deliver Therapeutic MicroRNAs to Presensitize Triple-Negative Breast Cancer to Doxorubicin.

Yi Liu, Uday K Sukumar, Masamitsu Kanada, Anandi Krishnan, Tarik F Massoud, Ramasamy Paulmurugan

Open access · greenAbstract read
In one paragraph

Article in Advanced functional materials, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
3.6field-weighted citation impact, top 6% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 58 citations in OpenAlex.

  1. Pooled it
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  5. Application of nanomedicines in tumor immunotherapy.Journal of molecular cell biology · 2025
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  20. Extracellular Vesicles (EVs) in Tumor Diagnosis and Therapy.Technology in cancer research & treatment
    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

6 authors at 4 institutions in 2 countries.

Yi LiuMolecular Imaging Program at Stanford (MIPS), Stanford University School of Medicine, Stanford, California.
Uday K SukumarMolecular Imaging Program at Stanford (MIPS), Stanford University School of Medicine, Stanford, California.
Masamitsu KanadaInstitute for Quantitative Health Science and Engineering (IQ), Michigan State University, East Lansing, MI 48824., USA.
Anandi KrishnanDepartment of Pathology, Stanford University School of Medicine, Stanford, California.
Tarik F MassoudMolecular Imaging Program at Stanford (MIPS), Stanford University School of Medicine, Stanford, California.
Ramasamy PaulmuruganMolecular Imaging Program at Stanford (MIPS), Stanford University School of Medicine, Stanford, California.
Stanford Medicine · USDalian Medical University · CNQuantitative BioSciences · USStanford University · US

Funding

Therapeutic miRNA Modulation of Hepatocellular Carcinoma Using Ultrasound Guided Drug DeliveryR01CA209888 · NCI · STANFORD UNIVERSITY · PI DAHL, JEREMY, PAULMURUGAN, RAMASAMY · 2017 to 2021
$3.1M
Integrated Clinical and Transcriptomic Profiling to Characterize Disease PhenotypeK08HG010061 · NHGRI · STANFORD UNIVERSITY · PI KRISHNAN, ANANDI · 2018 to 2022
$955k
3D Passive Cavitation Imaging-Guided Therapeutic Delivery of MicroRNA into CancerR21EB022298 · NIBIB · STANFORD UNIVERSITY · PI PAULMURUGAN, RAMASAMY · 2016 to 2017
$441k
Celigo S Imaging Cytometer (200-BFFL-S)S10OD023518 · OD · STANFORD UNIVERSITY · PI PAULMURUGAN, RAMASAMY · 2018 to 2018
$174k
NCI NIH HHS R01 CA209888NHGRI NIH HHS K08 HG010061NIBIB NIH HHS R21 EB022298NIH HHS S10 OD023518
6 · The paper itself

Abstract

Camouflaged cell-membrane-based nanoparticles have been gaining increasing attention owing to their improved biocompatibility and immunomodulatory properties. Using nanoparticles prepared from the membranes of specific cell types, or fusions derived from different cells membranes, can improve their functional performance in several aspects. Here, we used cell membranes extracted from breast cancer cells and platelets to fabricate a hybrid-membrane vesicle fusion (cancer cell-platelet-fusion-membrane vesicle, CPMV) in which we loaded therapeutic microRNAs (miRNAs) for the treatment of triple-negative breast cancer (TNBC). We used a clinically scalable microfluidic platform for the fusion of cell membranes. The reconstitution process during synthesis allows for efficient loading of miRNAs into CPMVs. We systematically optimized the conditions for preparation of miRNA-loaded CPMVs and demonstrated their property of homing to source cells using

Indexed as

Cancer cell-platelet membrane fusion vesiclechemotherapydoxorubicinmicrofluidicsmicroRNAspresensitizationtriple-negative breast cancer

Identifiers

PMID34899115
PMCPMC8664068
OpenAlexW3183271164

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.