Evidence map›Paper›PMID 29440899›Full record

ArticleInternational journal of nanomedicine2018

Aptamer-drug conjugate: targeted delivery of doxorubicin in a HER3 aptamer-functionalized liposomal delivery system reduces cardiotoxicity.

Xiao-Qian Dou, Hua Wang, Jing Zhang, Fang Wang, Gui-Li Xu, Cheng-Cheng Xu, Huan-Hua Xu, Shen-Si Xiang, Jie Fu, Hai-Feng Song

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
4.3field-weighted citation impact, top 4% 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

30 citing papers in PubMed, 79 citations in OpenAlex.

  1. Review
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  14. Rapid Detection ofACS omega · 2021
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  15. Review
  16. Emerging Significance and Therapeutic Potential of Extracellular vesicles.International journal of biological sciences · 2021
    Review
  17. Article
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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

10 authors at 1 institution in 1 country.

Xiao-Qian DouDepartment of Pharmacology and Toxicology, Beijing Institute of Radiation Medicine, Beijing, China.
Hua WangOphthalmology Department, Eye Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Jing ZhangBioanalysis Department, United-Power Pharma Tech Co., Ltd., Beijing, China.
Fang WangBioanalysis Department, United-Power Pharma Tech Co., Ltd., Beijing, China.
Gui-Li XuDepartment of Pharmacology and Toxicology, Beijing Institute of Radiation Medicine, Beijing, China.
Cheng-Cheng XuDepartment of Pharmacology and Toxicology, Beijing Institute of Radiation Medicine, Beijing, China.
Huan-Hua XuDepartment of Pharmacology and Toxicology, Beijing Institute of Radiation Medicine, Beijing, China.
Shen-Si XiangDepartment of Pharmacology and Toxicology, Beijing Institute of Radiation Medicine, Beijing, China.
Jie FuDepartment of Pharmacology and Toxicology, Beijing Institute of Radiation Medicine, Beijing, China.
Hai-Feng SongDepartment of Pharmacology and Toxicology, Beijing Institute of Radiation Medicine, Beijing, China.
Beijing Radiation Center · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe toxic side effects of doxorubicin (DOX) have limited its use in chemotherapy. Neither liposomal DOX nor pegylated liposomal DOX are able to completely resolve this issue. This is a proof-of-concept study testing aptamer-drug conjugate (ApDC) targeted delivery systems for chemotherapeutic drugs.

methodsAptamer library targeting human epidermal growth factor receptor 3 (HER3) was screened and affinity was determined by enzyme-linked immunosorbent assay. Specificity was tested in MCF-7

resultsThe candidate #13 aptamer had highest affinity (Kd =98±9.7 nM) and specificity. ApDC effectively reduces the half maximal inhibitory concentration of DOX compared with lipsome-DOX and free DOX. In vivo imaging and preliminary distribution studies showed that actively targeted nanoparticles, such as Apt-Lip-DOX molecules, could facilitate the delivery of DOX into tumors in MCF-7-bearing mice. This targeted chemotherapy caused greater tumor suppression than other groups and alleviated side effects such as weight loss, low survival rate, and organ (heart and liver) injury demonstrated by H&E staining.

conclusionThe results indicate that targeted chemotherapy using the aptamer-drug conjugate format could provide better tolerability and efficacy compared with non-targeted delivery in relatively low-dose toxic drugs.

Indexed as

AnimalsAntibiotics, AntineoplasticAptamers, NucleotideCardiotoxicityCell Line, TumorCell SurvivalDoxorubicinDrug Delivery SystemsEnzyme-Linked Immunosorbent AssayFemaleHumansLiposomesMCF-7 CellsMice, Inbred BALB CNanoparticlesPolyethylene GlycolsAntibiotics, AntineoplasticAptamers, NucleotideDoxorubicinERBB3 protein, humanliposomal doxorubicinLiposomesPolyethylene GlycolsReceptor, ErbB-3aptamer-drug conjugatebreast cancercardiac toxicitydoxorubicinhuman epidermal growth factor receptor 3targeted therapy

Identifiers

PMID29440899
PMCPMC5804143
OpenAlexW2792396136

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Registered trials

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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.