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dc.contributor.authorShariati, M
dc.contributor.authorAghaei, M
dc.contributor.authorMovahedian, A
dc.contributor.authorSomi, MH
dc.contributor.authorDolatkhah, H
dc.contributor.authorAghazade, AM
dc.date.accessioned2018-08-26T09:38:25Z
dc.date.available2018-08-26T09:38:25Z
dc.date.issued2016
dc.identifier10.4103/1735-1995.177358
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/58198
dc.description.abstractBACKGROUND: Studies show that polyunsaturated fatty acids (PUFAs) may have an inhibitory role in carcinogenesis. It was previously shown that PLA2 group 2A (PLA2G2A) messenger RNA (mRNA) expression is associated with less frequent metastasis and longer survival in gastric adenocarcinoma. This study intends to investigate the effect of PUFAs on the expression of PLA2G2A in patients with gastric cancer. MATERIALS AND METHODS: Thirty-four patients with gastric cancer (GC) were randomly divided into two groups. The first group received cisplatin medication. The second group received cisplatin medication and supplements of ω-fatty acids for three courses. The total RNA was extracted from the tissues and cDNA was synthesized. The gene expression of PLA2G2A was evaluated by the real-time polymerase chain reaction (PCR) method. To confirm the changes in gene expression, frozen section was utilized. The frozen tissue samples were sectioned and stained using the immunohistochemistry technique. RESULTS: After chemotherapy and chemotherapy plus supplement, the relative mean of PLA2G2A gene expression increased 1.5 ± 0.5-fold and 7.4 ± 2.6-fold, respectively (P = 0.006). The relative mean of gene expression in patients who received cisplatin and ω-fatty acids supplement increased more significantly (7.5 ± 3.3-fold) than in patients who received only cisplatin (P = 0.016). CONCLUSION: It was found that PUFAs increased the gene and protein expression of PLA2G2A in gastric cancer. Concerning the fact that studies reveal protective function of PLA2G2A in gastric cancer, it is suggested that increased expression of PLA2G2A is helpful. Furthermore, PUFAs can be considered as a useful therapeutic supplement for patients with gastric cancer.
dc.language.isoEnglish
dc.relation.ispartofJournal of Research in Medical Sciences
dc.subjectarachidonic acid
dc.subjectborage oil
dc.subjectcisplatin
dc.subjectcomplementary DNA
dc.subjectfish oil
dc.subjecticosapentaenoic acid
dc.subjectlinoleic acid
dc.subjectlinolenic acid
dc.subjectlinseed oil
dc.subjectomega 3 fatty acid
dc.subjectomega 6 fatty acid
dc.subjectphospholipase A2 group II
dc.subjectpolyunsaturated fatty acid
dc.subjectcisplatin
dc.subjectcomplementary DNA
dc.subjectmessenger RNA
dc.subjectomega 3 fatty acid
dc.subjectomega 6 fatty acid
dc.subjectadult
dc.subjectArticle
dc.subjectcancer patient
dc.subjectclinical article
dc.subjectcontrolled study
dc.subjectfatty acid analysis
dc.subjectfemale
dc.subjectgene expression
dc.subjecthuman
dc.subjecthuman tissue
dc.subjectimmunohistochemistry
dc.subjectmale
dc.subjectprotein expression
dc.subjectreal time polymerase chain reaction
dc.subjectRNA isolation
dc.subjectstomach cancer
dc.subjectaged
dc.subjectcancer chemotherapy
dc.subjectcomputer assisted tomography
dc.subjectendoscopy
dc.subjectgene
dc.subjectgene expression
dc.subjectPLA2G2A gene
dc.subjectprotein expression
dc.subjectRNA analysis
dc.subjectstomach biopsy
dc.subjectstomach cancer
dc.titleThe effect of ω-fatty acids on the expression of phospholipase A2 group 2A in human gastric cancer patients
dc.typeArticle
dc.citation.volume21
dc.citation.issue1
dc.citation.indexScopus
dc.identifier.DOIhttps://doi.org/10.4103/1735-1995.177358


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