EFFECT OF UROKINASE GENE KNOCKOUT ON TISSUE LEVELS OF BIOGENIC AMINES IN MICE WITH MELANOMA
Elena Mikhaylovna FRANTSIYANTS, Irina Viktorovna KAPLIEVA, Ekaterina Igorevna SURIKOVA, Irina Valerievna NESKUBINA, Valeriya Akhtyamovna BANDOVKINA, Lidia Konstantinovna TREPITAKI, Yuliya Aleksandrovna POGORELOVA, Lyudmila Anatolievna NEMASHKALOVA
Rostov Research Institute of Oncology
Keywords: биогенные амины, кожа, меланома, головной мозг, нокаут по гену uPA, мыши, biogenic amines, skin, melanoma, brain, uPA gene knockout, mice
Abstract
The research aim was to
study the dynamics of biogenic amines in the brain, tumor and intact
skin of urokinase (uPA) gene knockout mice on day 21 of the B16/F10
melanoma growth. Material and methods. The study included male and
female uPA gene knockout (-uPA, n = 38) and wild type mice (+uPA, n =
61). Melanoma was transplanted subcutaneously. Levels of biogenic amines
were studied by ELISA in tissues obtained on day 21 of carcinogenesis.
Results and discussion. Intact (-uPA) mice showed an increased total
content of biogenic amines: in the skin - due to noradrenaline increase
by 4.8 times in males and by 4.9 times in females, histamine - by 3.6
times in males and by 1.6 times ( p < 0.05) in females, serotonin -
by 3.4 times in males and by 8.3 times in females; in the brain - due to
noradrenaline increase by 3.5 times in males and by 3.2 times in
females, dopamine by 2.1 times in males and by 2.9 times in females,
while histamine content decreased. Melanoma development in (-uPA) mice
was characterized by: lower levels of adrenaline with high NA
concentrations and an increase in the serotonin metabolism in the brain;
higher histamine concentrations in the tumor and higher serotonin
levels in the skin; similar to (+uPA) mice levels of adrenaline (males)
and noradrenaline in the tumor and higher levels of adrenaline in the
tumor and histamine in the skin in (-uPA) females. Conclusions. The uPA
gene knockout limits the development of stress at the central regulatory
level due to lower levels of A together with increasing serotoninergic
mediation in the brain, as well as modulates the immune antitumor
response due to higher levels of histamine in the tumor and 5 serotonin
in the skin, as a result of lower monoamine oxidase activity, in mice
with B16/F10 melanoma.
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