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Authors Wu J, Cui Y, Zhang X, Gui L, Wang Y, Peng S, Zhao M
Received 14 September 2018
Accepted for publication 20 March 2019
Published 30 April 2019 Volume 2019:14 Pages 3027—3041
DOI https://doi.org/10.2147/IJN.S187600
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Cristina Weinberg
Peer reviewer comments 2
Editor who approved publication: Dr Lei Yang
Background: In the
discovery of DNA intercalators, β-carbolines compose one member of the most
interesting alkaloid family and are of clinical importance. In the efforts,
N-(3-benzyloxycarbonyl-β-carboline-1-yl)ethyl-Ser-Ala-OBzl (BCESA) was designed
as a nano-scaled DNA intercalator without Dox-like toxicity.
Methods: Based on
the structural analysis and CDOCKER energy comparison, BCESA was rationally
designed as such a nano-scaled intercalator. The anti-tumor activity, the
toxicity and the tumor targeting action of BCESA were evaluated on mouse
models.
Results: The in
vitro proliferation of cancer cells, but not non-cancer cells, was effectively
inhibited by BCESA. On S180 mouse model BCESA dose-dependently slowed the tumor
growth, and 0.01 μmol/kg/day was found as a minimal effective dose. Both BCESA
and its moiety were found in the tumor tissue, but not in the organs and the
blood, of S180 mice.
Conclusion: BCESA
should be a nano-scaled intercalator capable of targeting tumor tissue to
release anti-tumoral β-carboline-3-carboxylic acid and its 1-methyl derivative,
while Ser-Ala-OBzl is a simple and desirable carrier.
Keywords: nano-medicine,
β-carboline, intercalator, d(AGACGTCT)2, anti-tumor
