THE TRIGGER COMPONENTS OF THE PROTEOLYTIC SYSTEM AND THEIR MODULATORS CONTENTS UNDER PANCREATIC PATHOLOGIES DEVELOPMENT
T.B.Synelnyk1, O.O.Kravchenko1, O.S. Kostiuk1, O.M.Savchuk1, S.A. Sukhodolia2, L.I. Ostapchenko1
- Taras Shevchenko National University of Kyiv,
Educational and Scientific Centre “Institute of Biology and
Medicine”, Ukraine
- National Pirogov Memorial Medical University of Vinnytsya, Ukraine
DOI: https://doi.org/10.15407/fz68.05.033
Abstract
The content of the plasminogen activation system components
(plasminogen, plasminogen tissue activator, and its inhibitor
PAI-1) was investigated as well as the concentration of
thrombomodulin, protein C, matrix metalproteinases (MMP
-1, -2, -3, -8, -9, -10) and their inhibitor TIMP, growth factors
content (such as transforming growth factor-β1, insulin-like
growth factor-1, fibroblasts growth factor-2) and cytokine
profile (interleukines IL-1β, -4, -6, -8, -10, tumor necrosis
factor, interferon-γ in patients with chronic pancreatitis (CP)
and pancreatic cancer (PC) were established. Khmelnitsky
Regional Clinical Hospital patients aged 28-89 were
selected for this study: 20 people with chronic pancreatitis
(group CP); 20 people with pancreatic cancer (group PC);
20 conditionally healthy persons (control). Blood plasma
samples and pancreatic tissue homogenates were obtained
from all the patients. The studied indicators’ content in the
experimental materials was determined by the enzyme-linked
immunosorbent assay using appropriate antibodies. At the
level of systemic circulation, a statistically significant increase
was found in most of the studied parameters under the CP
conditions. However, PC was characterized by an increase
of two blood plasma indications only (thrombomodulin
and protein C). In contrast, the pancreatic sample tissue
examination for both aforementioned pathologies revealed
significant changes in the content of most metalloproteinases
and cytokines under PC. This indicates the development of
metastasis, angiogenesis, and immunomodulation-aimed local
biochemical processes in the affected organ.
Keywords:
chronic pancreatitis; pancreatic cancer; matrix metalloproteinases; cytokines; plasminogen; growth factors.
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