Evidence map›Paper›PMID 28845698›Full record

ArticleDrug delivery2017

Novel CD123-aptamer-originated targeted drug trains for selectively delivering cytotoxic agent to tumor cells in acute myeloid leukemia theranostics.

Haibin Wu, Meng Wang, Bo Dai, Yanmin Zhang, Ying Yang, Qiao Li, Mingyue Duan, Xi Zhang, Xiaomei Wang, Anmao Li and 1 more

Open access · goldAbstract read
In one paragraph

Article in Drug delivery, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

17 citing papers in PubMed, 30 citations in OpenAlex.

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  17. [Research advances in the role of aptamers in the diagnosis and targeted therapy of pediatric cancer].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2018
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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

11 authors at 2 institutions in 1 country.

Haibin Wua Shaanxi Institute of Pediatric Diseases , Xi'an Children's Hospital , Xi'an , Shaanxi , People's Republic of China.
Meng Wangc Department of Orthopedics , The No.11 Hospital of PLA , YiNing , XinJiang , People's Republic of China.
Bo Daid Shaanxi Center for Stem Cell Application Engineering Research , Xi'an , Shaanxi , People's Republic of China.
Yanmin Zhanga Shaanxi Institute of Pediatric Diseases , Xi'an Children's Hospital , Xi'an , Shaanxi , People's Republic of China.
Ying Yanga Shaanxi Institute of Pediatric Diseases , Xi'an Children's Hospital , Xi'an , Shaanxi , People's Republic of China.
Qiao Lif Clinical Laboratory , Xi'an Children's Hospital , Xi'an , Shaanxi , People's Republic of China.
Mingyue Duana Shaanxi Institute of Pediatric Diseases , Xi'an Children's Hospital , Xi'an , Shaanxi , People's Republic of China.
Xi Zhanga Shaanxi Institute of Pediatric Diseases , Xi'an Children's Hospital , Xi'an , Shaanxi , People's Republic of China.
Xiaomei Wanga Shaanxi Institute of Pediatric Diseases , Xi'an Children's Hospital , Xi'an , Shaanxi , People's Republic of China.
Anmao Lia Shaanxi Institute of Pediatric Diseases , Xi'an Children's Hospital , Xi'an , Shaanxi , People's Republic of China.
Liyu Zhanga Shaanxi Institute of Pediatric Diseases , Xi'an Children's Hospital , Xi'an , Shaanxi , People's Republic of China.
Xi’an Children’s Hospital · CNXi'an Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Since conventional chemotherapy for acute myeloid leukemia (AML) has its limitations, a theranostic platform with targeted and efficient drug transport is in demand. In this study, we developed the first CD123 (AML tumor marker) aptamers and designed a novel CD123-aptamer-mediated targeted drug train (TDT) with effective, economical, biocompatible and high drug-loading capacity. These two CD123 aptamers (termed as ZW25 and CY30, respectively) can bind to a CD123 peptide epitope and CD123 + AML cells with high specificities and KD of 29.41 nM and 15.38 nM, respectively, while has minimal cross reactivities to albumin, IgG and trypsin. Further, TDT is self-assembled from two short primers by ligand-modified ZW25 that acted as initiation position for elongation, while intercalated by doxorubicin (Dox). TDT is capable of transporting high capacity of Dox to CD123 + cells and retains the efficacy of Dox, while significantly reducing drug uptake and eased toxicity to CD123- cells in vitro (p < .01). Moreover, TDT can ease Dox cytoxicity to normal tissues, prolong survivals and inhibit tumor growth of mouse xenograft tumor model in vivo. These suggest that CD123 aptamer and CD123 aptamer-mediated targeted drug delivery system may have potential applications for selective delivery cytotoxic agents to CD123-expressing tumors in AML theranostics.

Indexed as

Leukemia, Myeloid, AcuteAnimalsAntineoplastic AgentsCell Line, TumorCytotoxinsHumansInterleukin-3 Receptor alpha SubunitMiceTheranostic NanomedicineAntineoplastic AgentsCytotoxinsInterleukin-3 Receptor alpha SubunitCD123 aptamerhigh drug loadingin vivoself-assemblytargeted drug train

Identifiers

PMID28845698
PMCPMC8241133
OpenAlexW2746461465

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.