Evidence map›Paper›PMID 26048585›Full record

ArticleToxicology and applied pharmacology2015

Safety evaluation of intravenously administered mono-thioated aptamer against E-selectin in mice.

Shin-Ae Kang, Bilegtsaikhan Tsolmon, Aman P Mann, Wei Zheng, Lichao Zhao, Yan Daniel Zhao, David E Volk, Ganesh L-R Lokesh, Lynsie Morris, Vineet Gupta and 5 more

Abstract read
In one paragraph

Article in Toxicology and applied pharmacology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed, 14 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

15 authors at 4 institutions in 1 country.

Shin-Ae KangStephenson Cancer Center, University of Oklahoma Health Sciences Center, 975 NE, 10th, Oklahoma City, OK 73104, United States.
Bilegtsaikhan TsolmonStephenson Cancer Center, University of Oklahoma Health Sciences Center, 975 NE, 10th, Oklahoma City, OK 73104, United States.
Aman P MannInstitute of Molecular Medicine, Department of NanoMedicine and Biomedical Engineering, University of Texas Health Science Center at Houston, 1825 Hermann Pressler, Houston, TX 77030, United States.
Wei ZhengStephenson Cancer Center, University of Oklahoma Health Sciences Center, 975 NE, 10th, Oklahoma City, OK 73104, United States.
Lichao ZhaoStephenson Cancer Center, University of Oklahoma Health Sciences Center, 975 NE, 10th, Oklahoma City, OK 73104, United States.
Yan Daniel ZhaoStephenson Cancer Center, University of Oklahoma Health Sciences Center, 975 NE, 10th, Oklahoma City, OK 73104, United States.
David E VolkInstitute of Molecular Medicine, Department of NanoMedicine and Biomedical Engineering, University of Texas Health Science Center at Houston, 1825 Hermann Pressler, Houston, TX 77030, United States.
Ganesh L-R LokeshInstitute of Molecular Medicine, Department of NanoMedicine and Biomedical Engineering, University of Texas Health Science Center at Houston, 1825 Hermann Pressler, Houston, TX 77030, United States.
Lynsie MorrisStephenson Cancer Center, University of Oklahoma Health Sciences Center, 975 NE, 10th, Oklahoma City, OK 73104, United States.
Vineet GuptaStephenson Cancer Center, University of Oklahoma Health Sciences Center, 975 NE, 10th, Oklahoma City, OK 73104, United States.
Wajeeha RazaqStephenson Cancer Center, University of Oklahoma Health Sciences Center, 975 NE, 10th, Oklahoma City, OK 73104, United States.
Hallgeir RuiThomas Jefferson University, 1020 Locust St, Philadelphia, PA 19107, United States.
K Stephen SuhJohn Theurer Cancer Center, Hackensack University Medical Center, Hackensack, NJ 07601, United States.
David G GorensteinInstitute of Molecular Medicine, Department of NanoMedicine and Biomedical Engineering, University of Texas Health Science Center at Houston, 1825 Hermann Pressler, Houston, TX 77030, United States.
Takemi TanakaStephenson Cancer Center, University of Oklahoma Health Sciences Center, 975 NE, 10th, Oklahoma City, OK 73104, United States. Electronic address: takemi-tanaka@ouhsc.edu.
University of Oklahoma Health Sciences Center · USThe University of Texas Health Science Center at Houston · USHackensack University Medical Center · USThomas Jefferson University · US

Funding

Texas Center for Cancer NanomedicineU54CA151668 · NCI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI FERRARI, MAURO · 2010 to 2014
$12.4M
Prolactin pathways and metastatic progression of ER-positive breast cancerR01CA188575 · NCI · THOMAS JEFFERSON UNIVERSITY · PI RUI, HALLGEIR · 2015 to 2019
$1.8M
Anti-Migration Therapy for Prevention and Treatment of Breast TumorR01CA160271 · NCI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI TANAKA, TAKEMI · 2012 to 2016
$1.6M
NCI NIH HHS 1R01CA160271-01A1NCI NIH HHS R01 CA160271NCI NIH HHS R01 CA188575NCI NIH HHS U54 CA151668NCI NIH HHS U54CA151668
6 · The paper itself

Abstract

The medical applications of aptamers have recently emerged. We developed an antagonistic thioaptamer (ESTA) against E-selectin. Previously, we showed that a single injection of ESTA at a dose of 100μg inhibits breast cancer metastasis in mice through the functional blockade of E-selectin. In the present study, we evaluated the safety of different doses of intravenously administered ESTA in single-dose acute and repeat-dose subacute studies in ICR mice. Our data indicated that intravenous administration of up to 500μg ESTA did not result in hematologic abnormality in either study. Additionally, intravenous injection of ESTA did not affect the levels of plasma cytokines (IL-1β, IL-2, IL-4, IL-5, IL-6, IL-10, GM-CSF, IFN-γ, and TNF-α) or complement split products (C3a and C5a) in either study. However, repeated injections of ESTA slightly increased plasma ALT and AST activities, in accordance with the appearance of small necrotic areas in the liver. In conclusion, our data demonstrated that intravenous administration of ESTA does not cause overt hematologic, organs, and immunologic responses under the experimental conditions.

Indexed as

Alanine TransaminaseAnimalsAntineoplastic AgentsAptamers, NucleotideAspartate AminotransferasesBiomarkersChemical and Drug Induced Liver InjuryComplement C3aComplement C5aCytokinesDose-Response Relationship, DrugDrug Administration ScheduleE-SelectinFemaleInjections, IntravenousKidneyAlanine TransaminaseAntineoplastic AgentsAptamers, NucleotideAspartate AminotransferasesBiomarkersComplement C3aComplement C5aCytokinesE-SelectinE-selectinMono-thioated aptamerSafetySystemic toxicity

Identifiers

PMID26048585
PMCPMC4966538
OpenAlexW1912294540

What OpenQuestion holds

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LicenceTDM
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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.