Title of article :
Study of the Effect of Linoleic Acid on the Expression Level of MicroRNA-106b and MicroRNA-20a and their Related Target MHC Class I Chain-related Protein A in Docetaxel-treated Gastric Cancer Cells
Author/Authors :
Shekari, Najibeh Department of Immunology - School of Medicine - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Kazemi, Tohid Immunology Research Center - Tabriz University of Medical Sciences, Tabriz, Iran , Moradi, Maedeh Immunology Research Center - Tabriz University of Medical Sciences, Tabriz, Iran , Eghbali, Elham Medical Radiation Sciences Research Group - Tabriz University of Medical Sciences, Tabriz, Iran , Sepehri, Bita Liver and Gastrointestinal Diseases Research Center - Tabriz University of Medical Sciences, Tabriz, Iran , Khaze Shahgoli, Vahid Department of Cancer and Inflammation Research - University of Southern Denmark, Odense, Denmark , Shirmohamadi, Masoud Liver and Gastrointestinal Diseases Research Center - Tabriz University of Medical Sciences, Tabriz, Iran
Abstract :
Background: MicroRNAs are involved in response to therapeutic agents and
have the ability to regulate the expression level of the targets associated with cancer
growth and progression. As a dangerous signal in tumor cells, increased expression
level of MHC class I chain-related protein A (MICA) could activate the immune
system and induce responses to tumor cells. We conducted the present research to
study the effect of linoleic acid (LA) and docetaxel alone or in combination with
miR-106b, miR-20a, and MICA expression level in metastatic gastric cancer (GC)
cell line MKN-45.
Method: The study was an in vitro study using the gastric cancer cell line MKN-
45, which was cultured and treated with docetaxel and LA. Subsequently, the expression
level of miR-106b, miR-20a, and MICA were assessed with quantitative real-time
polymerase chain reaction.
Results: MiR-106b decreased in LA and LA/docetaxel (P<0.0001 and P=0.002),
and increased in docetaxel alone (P = 0.01). Meanwhile, miR-20a significantly decreased
in docetaxel and LA/docetaxel (P<0.0001), increased in LA treatment (P=0.02).
Regarding MICA, it significantly decreased in all the treated cells (P<0.0001, P<0.0001,
and P=0.0002 for docetaxel, LA and docetaxel/LA, respectively) but with different
reduction intensities.
Conclusion: Using LA or docetaxel alone had a different effect on miR-106b,
miR-20a, and MICA expression level, yet in a simultaneous treatment, their positive
effects were intensified. LA enhanced the effect of docetaxel concerning the expression
level of miR-106b, miR-20a, and MICA and vice versa, which suggested that LA
could be employed as an effective complementary agent in GC along with docetaxel.
Keywords :
Linoleic acid , Docetaxel , miR-106b , miR-20a , MICA
Journal title :
Middle East Journal of Cancer (MEJC)