Synergistic Beneficial Effect of Docosahexaenoic Acid (DHA) and Docetaxel on the Expression Level of Matrix Metalloproteinase-2 (MMP-2) and MicroRNA-106b in Gastric Cancer.
Adenocarcinoma
/ genetics
Antineoplastic Combined Chemotherapy Protocols
/ pharmacology
Cell Line, Tumor
Docetaxel
/ pharmacology
Docosahexaenoic Acids
/ pharmacology
Down-Regulation
/ drug effects
Drug Synergism
Gene Expression Regulation, Neoplastic
/ drug effects
Humans
Matrix Metalloproteinase 2
/ genetics
MicroRNAs
/ genetics
Stomach Neoplasms
/ genetics
Talin
/ genetics
Up-Regulation
/ drug effects
DHA
Docetaxel
Gastric cancer
MMP-2
Talin-2
Journal
Journal of gastrointestinal cancer
ISSN: 1941-6636
Titre abrégé: J Gastrointest Cancer
Pays: United States
ID NLM: 101479627
Informations de publication
Date de publication:
Mar 2020
Mar 2020
Historique:
pubmed:
27
1
2019
medline:
11
7
2020
entrez:
26
1
2019
Statut:
ppublish
Résumé
Gastric cancer (GC) is one of the most common cancers with the majority of patients recognized in advanced stages. The efficacy of using docosahexaenoic acid (DHA) as a supplementary agent has been suggested in treatment along with chemotherapeutics including docetaxel. However, the molecular signatures of such beneficial effects are not well-understood. We aimed to evaluate the effects of DHA and docetaxel on the expression level of metastasis-related genes, including MMP-2 and talin-2, and their controlling miRNAs, miR-106b and miR-194, in metastatic GC cell line, MKN45. GC cell line, MKN45, was cultured, and determination of IC50 of DHA was done by MTT test. Cells were treated with docetaxel, DHA, and their combination for 24 h, and then total RNA was extracted and cDNA synthesis was done using standard protocols. The expression level of target genes, MMP-2 and talin-2, and miR-106b and miR-194 were determined by using quantitative real-time PCR. The expression level of MMP-2 was decreased significantly in all treated cells. However, talin-2 showed significant downregulation only after treatment with docetaxel. In contrary to increased expression after treatment with docetaxel, DHA led to a significant under-expression of miR-106b. The similar effect was seen for miR-194. Combination of docetaxel and DHA led to the significant downregulation of MMP-2. Also, DHA lowered the docetaxel-mediated upregulation of miR-106b oncomiR. In conclusion, supplementation of docetaxel therapy with DHA in GC patients would be considered as a beneficial approach in cancer treatment.
Sections du résumé
BACKGROUND
BACKGROUND
Gastric cancer (GC) is one of the most common cancers with the majority of patients recognized in advanced stages. The efficacy of using docosahexaenoic acid (DHA) as a supplementary agent has been suggested in treatment along with chemotherapeutics including docetaxel. However, the molecular signatures of such beneficial effects are not well-understood.
OBJECTIVE(S)
OBJECTIVE
We aimed to evaluate the effects of DHA and docetaxel on the expression level of metastasis-related genes, including MMP-2 and talin-2, and their controlling miRNAs, miR-106b and miR-194, in metastatic GC cell line, MKN45.
METHOD(S)
METHODS
GC cell line, MKN45, was cultured, and determination of IC50 of DHA was done by MTT test. Cells were treated with docetaxel, DHA, and their combination for 24 h, and then total RNA was extracted and cDNA synthesis was done using standard protocols. The expression level of target genes, MMP-2 and talin-2, and miR-106b and miR-194 were determined by using quantitative real-time PCR.
RESULTS
RESULTS
The expression level of MMP-2 was decreased significantly in all treated cells. However, talin-2 showed significant downregulation only after treatment with docetaxel. In contrary to increased expression after treatment with docetaxel, DHA led to a significant under-expression of miR-106b. The similar effect was seen for miR-194.
CONCLUSION(S)
CONCLUSIONS
Combination of docetaxel and DHA led to the significant downregulation of MMP-2. Also, DHA lowered the docetaxel-mediated upregulation of miR-106b oncomiR. In conclusion, supplementation of docetaxel therapy with DHA in GC patients would be considered as a beneficial approach in cancer treatment.
Identifiants
pubmed: 30680612
doi: 10.1007/s12029-019-00205-0
pii: 10.1007/s12029-019-00205-0
doi:
Substances chimiques
MIRN106 microRNA, human
0
MIRN194 microRNA, human
0
MicroRNAs
0
TLN2 protein, human
0
Talin
0
Docetaxel
15H5577CQD
Docosahexaenoic Acids
25167-62-8
Matrix Metalloproteinase 2
EC 3.4.24.24
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
70-75Subventions
Organisme : Research Center for Infectious Diseases and Tropical Medicine, Tabriz University of Medical Sciences
ID : 13098
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