IL-4, IL-17 and CD163 Immunoexpression and IL-6 Gene Polymorphism in Chronic Hepatitis C Patients and Associated Hepatocellular Carcinoma.
Antigens, CD
/ metabolism
Antigens, Differentiation, Myelomonocytic
/ metabolism
Biomarkers, Tumor
/ metabolism
Carcinoma, Hepatocellular
/ genetics
Genetic Predisposition to Disease
Genotype
Hepatitis C, Chronic
/ genetics
Humans
Interleukin-17
/ metabolism
Interleukin-4
/ metabolism
Interleukin-6
/ genetics
Liver Neoplasms
/ genetics
Receptors, Cell Surface
/ metabolism
CD136
HCV
IL-17
IL-4
IL-6
Journal
Asian Pacific journal of cancer prevention : APJCP
ISSN: 2476-762X
Titre abrégé: Asian Pac J Cancer Prev
Pays: Thailand
ID NLM: 101130625
Informations de publication
Date de publication:
01 Apr 2021
01 Apr 2021
Historique:
received:
21
11
2020
entrez:
28
4
2021
pubmed:
29
4
2021
medline:
6
11
2021
Statut:
epublish
Résumé
To assess the expression of IL-4, IL-17 and CD-163 as well as study of IL6-572 C/G gene polymorphism in chronic HCV and HCC on top of HCV. Sixty HCC specimens and 60 adjacent hepatic tissue with HCV of different grades of necro-inflammation and different stages of fibrosis. In addition to 55 HCV, 60 HCC and 50 healthy venous blood samples for evaluation of IL6-572 C/G gene polymorphism. high expression of IL-4, IL-17 and CD163 in higher grades of activity, late stages of fibrosis and higher degrees of steatosis of HCV. IL-4 and CD163 showed higher expression in advanced grades of HCC, while IL-17 more expressed in lower grades. No significant difference in IL6-572 C/G gene polymorphism among studied groups regarding G/C, G/G, C/C frequencies or G and C allele's frequencies. IL-4, IL-17 and CD163 were associated with HCV severity. Their expression in HCC suggests their important role in HCC development. Blocking of these proteins may be a good target to control inflammation in HCV and can hinder progression to cirrhosis then to HCC. On the other hand, IL6-572 promoter gene polymorphism is neither associated with HCV infection nor with HCC development and its progression.<br />.
Identifiants
pubmed: 33906302
doi: 10.31557/APJCP.2021.22.4.1105
pmc: PMC8325124
pii:
doi:
Substances chimiques
Antigens, CD
0
Antigens, Differentiation, Myelomonocytic
0
Biomarkers, Tumor
0
CD163 antigen
0
Interleukin-17
0
Interleukin-6
0
Receptors, Cell Surface
0
Interleukin-4
207137-56-2
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1105-1113Références
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