Evidence map›Paper›PMID 29217761›Full record

ArticleCancer research2018

Aptamer-Conjugated Extracellular Nanovesicles for Targeted Drug Delivery.

Yuan Wan, Lixue Wang, Chuandong Zhu, Qin Zheng, Guoxiang Wang, Jinlong Tong, Yuan Fang, Yiqiu Xia, Gong Cheng, Xia He and 1 more

Abstract read
In one paragraph

Article in Cancer research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 123 papers.

0numbers the graph read from it
0cells of the map it votes in
123citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

123 citing papers in PubMed, 245 citations in OpenAlex.

  1. Trial
  2. Review
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  4. Extracellular Vesicles and Their Role in Osteogenesis.Bioengineering (Basel, Switzerland) · 2026
    Review
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63 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

11 authors at 4 institutions in 2 countries.

Yuan Wan *Department of Biomedical Engineering, Micro and Nano Integrated Biosystem (MINIBio) Laboratory, The Pennsylvania State University, University Park, Pennsylvania. sxz10@psu.edu hexiabm@163.com.
Lixue Wang *The Second Affiliated Hospital of Southeast University, Nanjing, Jiangsu, China.
Chuandong ZhuThe Second Affiliated Hospital of Southeast University, Nanjing, Jiangsu, China.
Qin ZhengThe Second Affiliated Hospital of Southeast University, Nanjing, Jiangsu, China.
Guoxiang WangZetect Biomedical Company, Nanjing, Jiangsu, China.
Jinlong TongThe Second Affiliated Hospital of Southeast University, Nanjing, Jiangsu, China.
Yuan FangThe Second Affiliated Hospital of Southeast University, Nanjing, Jiangsu, China.
Yiqiu XiaDepartment of Biomedical Engineering, Micro and Nano Integrated Biosystem (MINIBio) Laboratory, The Pennsylvania State University, University Park, Pennsylvania.
Gong ChengDepartment of Biomedical Engineering, Micro and Nano Integrated Biosystem (MINIBio) Laboratory, The Pennsylvania State University, University Park, Pennsylvania.
Xia HeJiangsu Cancer Hospital & Jiangsu Institute of Cancer Research & Nanjing Medical University Affiliated Cancer Hospital, Nanjing, Jiangsu, China. sxz10@psu.edu hexiabm@163.com.
Si-Yang ZhengDepartment of Biomedical Engineering, Micro and Nano Integrated Biosystem (MINIBio) Laboratory, The Pennsylvania State University, University Park, Pennsylvania. sxz10@psu.edu hexiabm@163.com.
Pennsylvania State University · USSecond Affiliated Hospital of Nanjing Medical University · CNJiangsu Cancer Hospital · CNJiangsu Shengze Hospital · CN

Funding

Integration of Flexible Micro Spring Array and High Throughput Microfluidics forDP2CA174508 · NCI · PENNSYLVANIA STATE UNIVERSITY, THE · PI ZHENG, SIYANG · 2012 to 2012
$2.2M
NCI NIH HHS DP2 CA174508
6 · The paper itself

Abstract

Extracellular nanovesicles (ENV) released by many cells contain lipids, proteins, and nucleic acids that contribute to intercellular communication. ENVs have emerged as biomarkers and therapeutic targets but they have also been explored as drug delivery vehicles. However, for the latter application, clinical translation has been limited by low yield and inadequate targeting effects. ENV vectors with desired targeting properties can be produced from parental cells engineered to express membrane-bound targeting ligands, or they can be generated by fusion with targeting liposomes; however, neither approach has met clinical requirements. In this study, we demonstrate that mechanical extrusion of approximately 10

Indexed as

Drug Delivery SystemsAnimalsAntineoplastic Agents, PhytogenicApoptosisAptamers, NucleotideBreast NeoplasmsCell ProliferationExtracellular VesiclesFemaleHumansLipidsMiceMice, Inbred BALB CMice, NudeNanoparticlesNucleolinAntineoplastic Agents, PhytogenicAptamers, NucleotideLipidsNucleolinPaclitaxelPhosphoproteinsRNA-Binding Proteins

Identifiers

PMID29217761
PMCPMC5811376
OpenAlexW2771762192

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.