Evidence map›Paper›PMID 28475311›Full record

ArticleBioconjugate chemistry2017

Targeting and Internalization of Liposomes by Bladder Tumor Cells Using a Fibronectin Attachment Protein-Derived Peptide-Lipopolymer Conjugate.

Young Lee, Erin Kischuk, Scott Crist, Timothy L Ratliff, David H Thompson

Open access · greenAbstract read
In one paragraph

Article in Bioconjugate chemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

8 citing papers in PubMed, 17 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Young LeePurdue University Center for Cancer Research, Multi-disciplinary Cancer Research Facility, Purdue University , 1203 West State Street, West Lafayette, Indiana 47907, United States.ORCID 0000-0002-7926-7546
Erin KischukPurdue University Center for Cancer Research, Multi-disciplinary Cancer Research Facility, Purdue University , 1203 West State Street, West Lafayette, Indiana 47907, United States.
Scott CristPurdue University Center for Cancer Research, Multi-disciplinary Cancer Research Facility, Purdue University , 1203 West State Street, West Lafayette, Indiana 47907, United States.
Timothy L RatliffPurdue University Center for Cancer Research, Multi-disciplinary Cancer Research Facility, Purdue University , 1203 West State Street, West Lafayette, Indiana 47907, United States.
David H ThompsonPurdue University Center for Cancer Research, Multi-disciplinary Cancer Research Facility, Purdue University , 1203 West State Street, West Lafayette, Indiana 47907, United States.ORCID 0000-0002-0746-1526
State Street (United States) · US

Funding

Transgenic Mouse Core Facility Shared Resource (TMCF-SR)P30CA023168 · NCI · PURDUE UNIVERSITY WEST LAFAYETTE · PI John Tesmer · 1985 to 2026
$43.4M
Development of Bioresponsive Lipids for Intracellular DeliveryR01GM087016 · NIGMS · PURDUE UNIVERSITY · PI THOMPSON, DAVID H · 2009 to 2012
$1.2M
NCI NIH HHS P30 CA023168NIGMS NIH HHS R01 GM087016
6 · The paper itself

Abstract

A synthetic peptidolipopolymer conjugate, incorporated into liposomes to promote specific binding to the fibronectin (FBN) matrix surrounding bladder tumor cells and promote cellular internalization of FBN-integrin complexes, is reported. The peptide promotes association with MB49 mouse model bladder tumor cells in a sequence-specific and concentration-dependent manner, with the maximum cell association occurring at 2 mol % RWFV-PEG2000-DSPE. Double PEGylation of the liposome membrane (i.e., 4 mol % mPEG1000-DSPE + 2 mol % RWFV-PEG2000-DSPE) enhanced binding by >1.6-fold, by improving ligand presentation on the liposome surface. The sequence specificity of the peptide-lipopolymer construct was confirmed by comparing liposomes containing RWFV-PEG2000-DSPE with scrambled and nonpeptidic lipopolymer liposomal formulations. MB49 tumor-bearing mice showed greater mean radiance values for FAP peptide-targeted liposomes in tumor-associated regions of interest than for nontargeted and scrambled peptide liposome formulations. These findings suggest that peptide-modified liposomes may be an attractive vehicle for targeted delivery to bladder tumors in vivo.

Indexed as

AnimalsAntibiotics, AntineoplasticCell ProliferationDoxorubicinDrug Delivery SystemsFibronectinsHumansLiposomesMiceOligopeptidesPeptide FragmentsPhagocytosisPhosphatidylethanolaminesPolyethylene GlycolsPolymersTumor Cells, Cultured1,2-distearoyl-sn-glycero-3-phosphoethanolamine-N-methoxy-poly(ethylene glycol 2000)Antibiotics, AntineoplasticDoxorubicinfibronectin attachment peptideFibronectinsFN1 protein, humanLiposomesOligopeptidesPeptide FragmentsPhosphatidylethanolaminesPolyethylene GlycolsPolymers

Identifiers

PMID28475311
PMCPMC6502482
OpenAlexW2610713404

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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.