Evidence map›Paper›PMID 29230043›Full record

ArticleNature nanotechnology2018

Nanoparticle orientation to control RNA loading and ligand display on extracellular vesicles for cancer regression.

Fengmei Pi, Daniel W Binzel, Tae Jin Lee, Zhefeng Li, Meiyan Sun, Piotr Rychahou, Hui Li, Farzin Haque, Shaoying Wang, Carlo M Croce and 3 more

Open access · greenAbstract read
In one paragraph

Article in Nature nanotechnology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 236 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
236citing papers in PubMed, 1 pooled it
14.4field-weighted citation impact, top 1% 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

236 citing papers in PubMed, 1 synthesis or guideline pooled it, 484 citations in OpenAlex.

  1. Pooled it
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  10. CRISPR Interference to Inhibit Oncogenes for Cancer Therapy.International journal of molecular sciences · 2026
    Review
  11. Review
  12. Exosomes as Emerging Nanocarriers for Targeted Cancer Therapy.International journal of nanomedicine · 2026
    Review
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  18. Article
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176 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

13 authors at 4 institutions in 1 country.

Fengmei PiCollege of Pharmacy, The Ohio State University, Columbus, OH, USA.
Daniel W BinzelCollege of Pharmacy, The Ohio State University, Columbus, OH, USA.
Tae Jin LeeComprehensive Cancer Center, The Ohio State University, Columbus, OH, USA.
Zhefeng LiCollege of Pharmacy, The Ohio State University, Columbus, OH, USA.
Meiyan SunDepartment of Pharmacological and Pharmaceutical Sciences, College of Pharmacy, University of Houston, Houston, TX, USA.
Piotr RychahouMarkey Cancer Center, Department of Surgery, University of Kentucky, Lexington, KY, USA.
Hui LiCollege of Pharmacy, The Ohio State University, Columbus, OH, USA.
Farzin HaqueCollege of Pharmacy, The Ohio State University, Columbus, OH, USA.
Shaoying WangCollege of Pharmacy, The Ohio State University, Columbus, OH, USA.
Carlo M CroceComprehensive Cancer Center, The Ohio State University, Columbus, OH, USA.
Bin GuoDepartment of Pharmacological and Pharmaceutical Sciences, College of Pharmacy, University of Houston, Houston, TX, USA.
B Mark EversMarkey Cancer Center, Department of Surgery, University of Kentucky, Lexington, KY, USA.
Peixuan GuoCollege of Pharmacy, The Ohio State University, Columbus, OH, USA. guo.1091@osu.edu.
Lung Institute · USThe Ohio State University · USUniversity of Houston · USUniversity of Kentucky · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Tasleem J Padamsee · 1985 to 2026
$132.3M
University of Kentucky Markey Cancer Center Support Grant ECIA SupplementP30CA177558 · NCI · UNIVERSITY OF KENTUCKY · PI KATHLEEN L. O'CONNOR · 2013 to 2026
$38.3M
Cancer Gene Discovery to Identify Targetable TargetsR35CA197706 · NCI · OHIO STATE UNIVERSITY · PI CROCE, CARLO M · 2015 to 2021
$6.4M
Optimizing RNA nanoparticles size and shape for enhancing cancer targeting and treatmentU01CA207946 · NCI · OHIO STATE UNIVERSITY · PI CARSON, WILLIAM E., GUO, PEIXUAN · 2016 to 2020
$2.7M
Fruit exosome-like particles for therapeutic delivery of extracellular miRNAsUH3TR000875 · NCATS · UNIVERSITY OF LOUISVILLE · PI ZHANG, HUANG-GE · 2015 to 2017
$2.7M
Echogenic Polymersomes for Triggered Contents ReleaseR01GM114080 · NIGMS · NORTH DAKOTA STATE UNIVERSITY · PI MALLIK, SANKU, SARKAR, KAUSIK · 2015 to 2023
$2.6M
Novel pRNA Nanoparticle Delivery as Directed Therapy for Colorectal Cancer MetastasisR01CA195573 · NCI · UNIVERSITY OF KENTUCKY · PI EVERS, BERNARD MARK, GUO, PEIXUAN · 2015 to 2019
$1.8M
RNA Therapeutics for Targeted Treatment of Colon CancerR01CA186100 · NCI · UNIVERSITY OF HOUSTON · PI GUO, BIN · 2015 to 2018
$1.4M
NCATS NIH HHS UH3 TR000875NCI NIH HHS P30 CA016058NCI NIH HHS P30 CA177558NCI NIH HHS R01 CA186100NCI NIH HHS R01 CA195573NCI NIH HHS R35 CA197706NCI NIH HHS U01 CA207946NIGMS NIH HHS R01 GM114080
6 · The paper itself

Abstract

Nanotechnology offers many benefits, and here we report an advantage of applying RNA nanotechnology for directional control. The orientation of arrow-shaped RNA was altered to control ligand display on extracellular vesicle membranes for specific cell targeting, or to regulate intracellular trafficking of small interfering RNA (siRNA) or microRNA (miRNA). Placing membrane-anchoring cholesterol at the tail of the arrow results in display of RNA aptamer or folate on the outer surface of the extracellular vesicle. In contrast, placing the cholesterol at the arrowhead results in partial loading of RNA nanoparticles into the extracellular vesicles. Taking advantage of the RNA ligand for specific targeting and extracellular vesicles for efficient membrane fusion, the resulting ligand-displaying extracellular vesicles were capable of specific delivery of siRNA to cells, and efficiently blocked tumour growth in three cancer models. Extracellular vesicles displaying an aptamer that binds to prostate-specific membrane antigen, and loaded with survivin siRNA, inhibited prostate cancer xenograft. The same extracellular vesicle instead displaying epidermal growth-factor receptor aptamer inhibited orthotopic breast cancer models. Likewise, survivin siRNA-loaded and folate-displaying extracellular vesicles inhibited patient-derived colorectal cancer xenograft.

Indexed as

RNAi TherapeuticsAnimalsAptamers, NucleotideCell Line, TumorDrug Delivery SystemsErbB ReceptorsExtracellular VesiclesHumansMaleMiceNanoparticlesProstatic NeoplasmsRNA, Small InterferingSurvivinAptamers, NucleotideErbB ReceptorsRNA, Small InterferingSurvivin

Identifiers

PMID29230043
PMCPMC5762263
OpenAlexW2774123716

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.