| Literature DB >> 26048585 |
Shin-Ae Kang1, Bilegtsaikhan Tsolmon1, Aman P Mann2, Wei Zheng1, Lichao Zhao1, Yan Daniel Zhao1, David E Volk2, Ganesh L-R Lokesh2, Lynsie Morris1, Vineet Gupta1, Wajeeha Razaq1, Hallgeir Rui3, K Stephen Suh4, David G Gorenstein2, Takemi Tanaka5.
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.Entities:
Keywords: E-selectin; Mono-thioated aptamer; Safety; Systemic toxicity
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Year: 2015 PMID: 26048585 PMCID: PMC4966538 DOI: 10.1016/j.taap.2015.05.011
Source DB: PubMed Journal: Toxicol Appl Pharmacol ISSN: 0041-008X Impact factor: 4.219