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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
  • Προβολή τεκμηρίου
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Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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Genetic polymorphisms of FAS and EVER genes in a Greek population and their susceptibility to cervical cancer: A case control study

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Συγγραφέας
Pavlidou E., Daponte A., Egea R., Dardiotis E., Hadjigeorgiou G.M., Barbadilla A., Agorastos T.
Ημερομηνία
2016
Γλώσσα
en
DOI
10.1186/s12885-016-2960-3
Λέξη-κλειδί
adult
Article
cancer susceptibility
case control study
cohort analysis
controlled study
EVER gene
FAS gene
female
gene expression
gene frequency
genetic association
genotype
Greek (people)
human
major clinical study
prospective study
single nucleotide polymorphism
uterine cervix carcinoma in situ
allele
cancer staging
gene linkage disequilibrium
genetic predisposition
genetics
Greece
middle aged
pathology
risk
uterine cervix tumor
Fas antigen
membrane protein
TMC6 protein, human
TMC8 protein, human
Adult
Alleles
Antigens, CD95
Case-Control Studies
Female
Gene Frequency
Genetic Predisposition to Disease
Genotype
Greece
Humans
Linkage Disequilibrium
Membrane Proteins
Middle Aged
Neoplasm Staging
Polymorphism, Single Nucleotide
Risk
Uterine Cervical Neoplasms
BioMed Central Ltd.
Εμφάνιση Μεταδεδομένων
Επιτομή
Background: The aim of the study was to evaluate the association of two SNPs of EVER1/2 genes' region (rs2290907, rs16970849) and the FAS-670 polymorphism with the susceptibility to precancerous lesions and cervical cancer in a Greek population. Methods: Among the 515 women who were included in the statistical analysis, 113 belong to the case group and present with precancerous lesions or cervical cancer (27 with persistent CIN1, 66 with CIN2/3 and 20 with cervical cancer) and 402 belong to the control group. The chi-squared test was used to compare the case and the control groups with an allelic and a genotype-based analysis. Results: The results of the statistical analysis comparing the case and the control groups for all the SNPs tested were not statistically significant. Borderline significant difference (p value = 0.079) was only found by the allelic model between the control group and the CIN1/CIN2 patients' subgroup for the polymorphism rs16970849. The comparison of the other case subgroups with the control group did not show any statistically significant difference. Conclusions: None of the SNPs included in the study can be associated with statistical significance with the development of precancerous lesions or cervical cancer. © 2016 The Author(s).
URI
http://hdl.handle.net/11615/77998
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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