Inhibitory Effect of Phosphorothioate Oligonucleotide Complementary to G6PD mRNA on Murine Melanoma

Author:

Yurchenko Kseniya A.1ORCID,Laikova Kateryna V.2,Golovkin Ilya O.2ORCID,Novikov Ilya A.1ORCID,Yurchenko Alyona A.1,Makalish Tatyana P.2,Oberemok Volodymyr V.1ORCID

Affiliation:

1. Department of Molecular Genetics and Biotechnologies, Institute of Biochemical Technologies, Ecology and Pharmacy, V.I. Vernadsky Crimean Federal University, 295007 Simferopol, Russia

2. Medical Academy Named after S.I. Georgievsky, V.I. Vernadsky Crimean Federal University, 295007 Simferopol, Russia

Abstract

In terms of the incidence among all tumors, skin cancer is on top, with the most deadly among them being melanoma. The search for new therapeutic agents to combat melanoma is very relevant. In our opinion, antisense oligonucleotides (ASO) aimed at suppressing the genes responsible for their viability in cancer cells give hope for treatment, which makes it possible to eliminate cancer cells near the tumor site both before and after surgery. In this article, we describe how Skeen-11 phosphorothioate oligonucleotide significantly decreased the proliferative activity of murine melanoma cells. Injections of Skeen-11 also inhibited tumor growth in mice with inoculated melanoma. A toxicity study showed no side effects with dose adjustments. The results show that the use of ASO Skeen-11 in vivo reduced the tumor size within 7 days, reduced the number of mitoses in the tumor cells, and increased the amount of necrosis compared with the control group.

Publisher

MDPI AG

Subject

General Medicine

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