Evidence map›Paper›PMID 25523519›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2015

Biodistribution and delivery efficiency of unmodified tumor-derived exosomes.

Tyson Smyth, Max Kullberg, Noeen Malik, Peter Smith-Jones, Michael W Graner, Thomas J Anchordoquy

Abstract read
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 391 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
391citing papers in PubMed, 1 pooled it
–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

391 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Modified tumor uptake and biodistribution of nanoparticles coated with small extracellular vesicle membranes derived from distinct tumor cell lines.International journal of hyperthermia : the official journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group · 2026
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  7. Extracellular vesicles: Navigating new frontiers in glioblastoma therapy.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2026
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331 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

6 authors.

Tyson SmythUniversity of Colorado Denver, Anschutz Medical Campus, Department of Pharmaceutical Sciences, Aurora, CO, USA.
Max KullbergUniversity of Colorado Denver, Anschutz Medical Campus, Department of Pharmaceutical Sciences, Aurora, CO, USA.
Noeen MalikUlm University Hospital, Clinic for Nuclear Medicine, Ulm, Germany.
Peter Smith-JonesStony Brook School of Medicine, Department of Psychiatry, Stony Brook, NY, USA.
Michael W GranerUniversity of Colorado Denver, Anschutz Medical Campus, Department of Neurosurgery, Aurora, CO, USA.
Thomas J AnchordoquyUniversity of Colorado Denver, Anschutz Medical Campus, Department of Pharmaceutical Sciences, Aurora, CO, USA. Electronic address: Tom.Anchordoquy@ucdenver.edu.

Funding

University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
LEADERSHIP TRAINING IN PHARMACEUTICAL BIOTECHNOLOGYT32GM008732 · NIGMS · UNIVERSITY OF COLORADO AT BOULDER · PI RANDOLPH, THEODORE W · 2001 to 2015
$2.7M
Tumor-Homing Exosomes for Drug DeliveryR01EB016378 · NIBIB · UNIVERSITY OF COLORADO DENVER · PI ANCHORDOQUY, THOMAS, GRANER, MICHAEL W. · 2013 to 2016
$1.5M
Exploiting Cholesterol Nanodomains to Improve TargetingR01GM093287 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI ANCHORDOQUY, THOMAS · 2011 to 2014
$1.1M
NCI NIH HHS P30 CA046934NIBIB NIH HHS 1R01EB016378-01A1NIBIB NIH HHS R01 EB016378NIGMS NIH HHS 1R01GM093287-01A1NIGMS NIH HHS 5 T32 GM 8732NIGMS NIH HHS R01 GM093287NIGMS NIH HHS T32 GM008732
6 · The paper itself

Abstract

The use of exosomes as a drug delivery vehicle has gained considerable interest. To establish if exosomes could be utilized effectively for drug delivery, a better understanding of their in vivo fate must be established. Through comparisons to liposomal formulations, which have been studied extensively for the last thirty years, we were able to make some comprehensive conclusions about the fate of unmodified tumor-derived exosomes in vivo. We observed a comparable rapid clearance and minimal tumor accumulation of intravenously-injected exosomes, PC:Chol liposomes, and liposomes formulated with the lipid extract of exosomes, suggesting that the unique protein and lipid composition of exosomes does not appreciably impact exosomes' rate of clearance and biodistribution. This rapid clearance along with minimal tumor accumulation of unmodified exosomes limits their use as an anti-cancer drug delivery vehicle; however, when delivered intratumorally, exosomes remained associated with tumor tissue to a significantly greater extent than PC:Chol liposomes. Furthermore, experiments utilizing mice with impaired adaptive or innate immune systems, revealed the significance of the innate immune system along with the complement protein C5 on exosomes' rate of clearance.

Indexed as

AnimalsAntibiotics, AntineoplasticAntineoplastic AgentsCell LineChemistry, PharmaceuticalCholineDoxorubicinDrug Delivery SystemsExosomesInjections, IntravenousLiposomesMiceMice, Inbred BALB CNeoplasmsParticle SizePharmaceutical VehiclesAntibiotics, AntineoplasticAntineoplastic AgentsCholineDoxorubicinLiposomesPharmaceutical VehiclesPhosphatidylcholinesBiodistributionExosomesIntratumoral injectionIntravenous injectionLiposomes

Identifiers

PMID25523519
PMCPMC4441346

What OpenQuestion holds

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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.