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1.
J Med Virol ; 95(1): e28309, 2023 01.
Article in English | MEDLINE | ID: mdl-36377303

ABSTRACT

There is a significant body of evidence showing that efficient vaccination schemes against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is helping control the coronavirus disease 2019 (COVID-19) pandemic. However, this goal cannot be achieved without real world data highlighting the impact of vaccines against viral spread. In this study, we have aimed at differentially investigating the impact of COVID-19 vaccines (CoronaVac, Pfizer/BioNTech, Astra/Zeneca Oxford, Janssen) used in North Cyprus in limiting the viral load of Delta and Omicron variants of SARS-COV-2. We have utilized real-time quantitative polymerase chain reaction cycle threshold values (Ct values) as a proxy of viral load of the two SARS-CoV-2 variants. Our results indicate that the administration of at least two doses of the messenger RNA-based Pfizer/BioNTech vaccine leads to the lowest viral load (highest Ct values) obtained for both Omicron and Delta variants. Interestingly, regardless of the vaccine type used, our study revealed that Delta variant produced significantly higher viral loads (lower Ct values) compared with the Omicron variant, where the latter was more commonly associated with younger patients. Viral spread is a crucial factor that can help determine the future of the pandemic. Thus, prioritizing vaccines that will play a role in not only preventing severe disease but also in limiting viral load and spread may contribute to infection control strategies.


Subject(s)
COVID-19 , Smallpox Vaccine , Vaccines , Humans , COVID-19 Vaccines , SARS-CoV-2/genetics , Viral Load , COVID-19/prevention & control
2.
Cent Eur J Public Health ; 29(2): 130-133, 2021 06.
Article in English | MEDLINE | ID: mdl-34245553

ABSTRACT

OBJECTIVES: Vitamin D is a fat-soluble, prohormone vitamin that is important especially for bone mineralization and skeletal health. In recent years, vitamin D deficiency appeared as a worldwide problem, affecting many people in different ways including the Northern Cypriot population. The deficiency might be caused by the lack of exposure to sunlight, diet low in vitamin D, sedentary lifestyle, and also due to some genetic variations in the vitamin D receptor (VDR) gene. METHODS: In this study, four common VDR polymorphisms and associations with vitamin D deficiency in the Turkish Cypriot population between ages 18-40 and working in office conditions was studied by PCR- RFLP analysis. RESULTS: rs2228570 C>T variant was shown to be significantly associated with low serum vitamin D levels in the studied population. CONCLUSION: Together with the effect of rs2228570 C>T variant in the VDR gene, it is thought that the lifestyle changes in the Turkish Cypriot population might have caused the increased frequency of vitamin D deficiency in the young professionals.


Subject(s)
Polymorphism, Single Nucleotide , Vitamin D Deficiency , Adolescent , Adult , Case-Control Studies , Genetic Predisposition to Disease , Genotype , Humans , Polymorphism, Restriction Fragment Length , Selection, Genetic , Vitamin D , Vitamin D Deficiency/epidemiology , Vitamin D Deficiency/genetics , Young Adult
3.
Curr Drug Metab ; 21(6): 466-470, 2020.
Article in English | MEDLINE | ID: mdl-32562520

ABSTRACT

BACKGROUND: The use of psychoactive substances is one of the most dangerous social problems worldwide. Nicotine dependence results from the interaction between neurobiological, environmental and genetic factors. Serotonin is a neurotransmitter that has a wide range of central nervous system activities. The serotonin transporter gene has been previously linked to psychological traits. OBJECTIVE: A variable number of tandem repeats within the serotonin transporter-linked polymorphic gene region are believed to alter the transcriptional efficiency of the 5-HTT gene. Therefore, we aimed to investigate the association between this polymorphic site and smoking behavior in the Turkish Cypriot population. METHODS: A total of 259 (100 smokers, 100 non-smokers and 59 ex-smokers) Turkish Cypriots were included in this population-based cross-sectional study. Genomic DNA was extracted from peripheral blood samples and the 5-HTTVNTR2 polymorphisms were determined by the PCR-RFLP. RESULTS: The allelic frequency and genotype distribution results of this study showed a strong association (P<0.0001) between smokers and non-smokers. No statistical significance was found between non-smokers and ex-smokers. CONCLUSION: This is the first genetic epidemiology study to investigate the allelic frequencies of 5-HTTVNTR2 polymorphisms associated with smoking behavior in the Turkish Cypriot population. Based on the results of this study, genome-wide association studies should be designed for preventive medicine in this population.


Subject(s)
Genetic Predisposition to Disease , Nicotine/metabolism , Serotonin Plasma Membrane Transport Proteins/genetics , Tobacco Use Disorder/genetics , Adult , Cross-Sectional Studies , Ex-Smokers/statistics & numerical data , Female , Gene Frequency , Genotyping Techniques , Humans , Male , Middle Aged , Non-Smokers/statistics & numerical data , Polymorphism, Genetic , Serotonin Plasma Membrane Transport Proteins/metabolism , Smokers/statistics & numerical data , Tobacco Use Disorder/epidemiology , Turkey/epidemiology
4.
PLoS One ; 9(8): e105278, 2014.
Article in English | MEDLINE | ID: mdl-25148256

ABSTRACT

c-Met, the receptor for Hepatocyte Growth Factor (HGF), overexpressed and deregulated in Hepatocellular Carcinoma (HCC). Caveolin 1 (CAV1), a plasma membrane protein that modulates signal transduction molecules, is also overexpressed in HCC. The aim of this study was to investigate biological and clinical significance of co-expression and activation of c-Met and CAV1 in HCC. We showed that c-Met and CAV1 were co-localized in HCC cells and HGF treatment increased this association. HGF-triggered c-Met activation caused a concurrent rise in both phosphorylation and expression of CAV1. Ectopic expression of CAV1 accelerated c-Met signaling, resulted in enhanced migration, invasion, and branching-morphogenesis. Silencing of CAV1 downregulated c-Met signaling, and decreased migratory/invasive capability of cells and attenuated branching morphogenesis. In addition, activation and co-localization of c-Met and CAV1 were elevated during hepatocarcinogenesis. In conclusion reciprocal activating crosstalk between c-Met and CAV1 promoted oncogenic signaling of c-Met contributed to the initiation and progression of HCC.


Subject(s)
Carcinoma, Hepatocellular/metabolism , Carcinoma, Hepatocellular/pathology , Caveolin 1/metabolism , Liver Neoplasms/metabolism , Liver Neoplasms/pathology , Proto-Oncogene Proteins c-met/metabolism , Carcinoma, Hepatocellular/genetics , Cell Line, Tumor , Cell Movement/drug effects , Cell Movement/genetics , Gene Expression Regulation, Neoplastic/drug effects , Gene Silencing , Hepatocyte Growth Factor/pharmacology , Humans , Liver Cirrhosis/genetics , Liver Cirrhosis/metabolism , Liver Cirrhosis/pathology , Liver Neoplasms/genetics , Neoplasm Invasiveness , Phosphorylation , Protein Binding , Protein Transport , Proto-Oncogene Proteins c-met/agonists , Proto-Oncogene Proteins c-met/antagonists & inhibitors , RNA Interference , Signal Transduction
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