Evidence map›Paper›PMID 30207473›Full record

ArticleNano letters2018

Leutusome: A Biomimetic Nanoplatform Integrating Plasma Membrane Components of Leukocytes and Tumor Cells for Remarkably Enhanced Solid Tumor Homing.

Hongliang He, Chunqing Guo, Jing Wang, William J Korzun, Xiang-Yang Wang, Shobha Ghosh, Hu Yang

Abstract read
In one paragraph

Article in Nano letters, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
6.6field-weighted citation impact, top 2% 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

63 citing papers in PubMed, 154 citations in OpenAlex.

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3 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

7 authors at 1 institution in 1 country.

Hongliang HeDepartment of Chemical and Life Science Engineering , Virginia Commonwealth University , Richmond , Virginia 23219 , United States.
Chunqing GuoDepartment of Human and Molecular Genetics , Virginia Commonwealth University , Richmond , Virginia 23298 , United States.
Jing WangDepartment of Internal Medicine , Virginia Commonwealth University , Richmond , Virginia 23298 , United States.
William J KorzunDepartment of Clinical Laboratory Sciences , Virginia Commonwealth University , Richmond , Virginia 23298 , United States.
Xiang-Yang WangDepartment of Human and Molecular Genetics , Virginia Commonwealth University , Richmond , Virginia 23298 , United States.
Shobha GhoshDepartment of Internal Medicine , Virginia Commonwealth University , Richmond , Virginia 23298 , United States.ORCID 0000-0001-9470-6933
Hu YangDepartment of Chemical and Life Science Engineering , Virginia Commonwealth University , Richmond , Virginia 23219 , United States.ORCID 0000-0003-3030-004X
Virginia Commonwealth University · US

Funding

Virus Vector Shared ResourceP30CA016059 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI Kim Felder Rhoads · 1985 to 2026
$51.0M
Center for Clinical and Translational ResearchUL1TR000058 · NCATS · VIRGINIA COMMONWEALTH UNIVERSITY · PI MOELLER, FREDERICK GERARD · 2012 to 2015
$12.5M
Cholesterol regulation of Macrophage Inflammation and Vascular DiseasesI01BX002297 · VA · VA VETERANS ADMINISTRATION HOSPITAL · PI GHOSH, SHOBHA · 2016 to 2019
–
BLRD VA I01 BX002297NCATS NIH HHS UL1 TR000058NCI NIH HHS P30 CA016059
6 · The paper itself

Abstract

Cell membrane-camouflaged nanoparticles have appeared as a promising platform to develop active tumor targeting nanomedicines. To evade the immune surveillance, we designed a composite cell membrane-camouflaged biomimetic nanoplatform, namely, leutusome, which is made of liposomal nanoparticles incorporating plasma membrane components derived from both leukocytes (murine J774A.1 cells) and tumor cells (head and neck tumor cells HN12). Exogenous phospholipids were used as building blocks to fuse with two cell membranes to form liposomal nanoparticles. Liposomal nanoparticles made of exogenous phospholipids only or in combination with one type of cell membrane were fabricated and compared. The anticancer drug paclitaxel (PTX) was used to make drug-encapsulating liposomal nanoparticles. Leutusome resembling characteristic plasma membrane components of the two cell membranes were examined and confirmed in vitro. A xenograft mouse model of head and neck cancer was used to profile the blood clearance kinetics, biodistribution, and antitumor efficacy of the different liposomal nanoparticles. The results demonstrated that leutusome obtained prolonged blood circulation and was most efficient accumulating at the tumor site (79.1 ± 6.6% ID per gram of tumor). Similarly, leutusome composed of membrane fractions of B16 melanoma cells and leukocytes (J774A.1) showed prominent accumulation within the B16 tumor, suggesting the generalization of the approach. Furthermore, PTX-encapsulating leutusome was found to most potently inhibit tumor growth while not causing systemic adverse effects.

Indexed as

AnimalsBiomimeticsCell Line, TumorCell MembraneDrug Delivery SystemsHumansLeukocytesLiposomesMelanoma, ExperimentalMiceNanoparticlesPaclitaxelTissue DistributionXenograft Model Antitumor AssaysLiposomesPaclitaxelActive targetingcell membrane camouflageleukocytesnanoparticlestumor cellstumor microenvironment

Identifiers

PMID30207473
PMCPMC6292712
OpenAlexW2891725231

What OpenQuestion holds

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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.