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Phosphorylation of Protein Kinase Akt by Mtorc2 in Peripheral Blood Mononuclear Cells of Patients with Cancer and Diabetes
Author(s) -
Т.С. Вацеба,
Л.К. Соколова,
Victor Volodymyrovich Pushkarev,
О.І. Ковзун,
V.M. Pushkarev,
Bogdan Bogdanovich Guda,
Mykola Dmytrovich Tronko
Publication year - 2019
Publication title -
journal of endocrinology research
Language(s) - English
Resource type - Journals
ISSN - 2630-5224
DOI - 10.30564/jer.v1i1.674
Subject(s) - protein kinase b , peripheral blood mononuclear cell , medicine , pi3k/akt/mtor pathway , cancer , diabetes mellitus , mtorc1 , cancer research , immunology , pathogenesis , mtorc2 , type 2 diabetes , phosphorylation , endocrinology , signal transduction , biology , microbiology and biotechnology , biochemistry , in vitro
Article history Received: 20 March 2019 Accepted: 23 April 2019 Published Online: 30 April 2019 Akt/mTOR/p70S6K1 signaling pathway plays an important role in the pathogenesis of cancer and diabetes. Macrophages and lymphocytes are involved in the pathogenesis of diabetes, diabetic atherosclerosis, formation of insulin resistance as well as immune response to cancer and tumor maintenance. The aim of the study was to determine the Akt activation by mTORC2 in peripheral blood mononuclear cell (PBMC) of patients with type 2 diabetes and cancer. The following groups were studied: control group, patients with type 2 diabetes, cancer patients and patients with both cancer and diabetes. The amounts of phospho-Akt (рS473) and phospho-p70S6K1 (p-T389) were determined using ELISA kits. The amount of phosphorylated Akt significantly increases in PBMC of patients with cancer. There was no effect in PBMC from patients with type 2 diabetes and significant decrease in the amount of phospho-Akt in PBMC of the patients group both with cancer and diabetes. p70S6K1 activation was observed in PBMC of the groups 2 and 3 patients. Thus, chronic diseases such as type 2 diabetes and cancer can affect the signaling mechanisms in blood cells. The state of Akt phosphorylation in leukocytes can indicate the activity of mTORC1 and its substrates, which may be important for the evaluation of the pathological process and the efficacy of the drugs.

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