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dc.contributor.authorKafshdooz, T
dc.contributor.authorTabrizi, AD
dc.contributor.authorMohaddes Ardabili, SM
dc.contributor.authorKafshdooz, L
dc.contributor.authorGhojazadeh, M
dc.contributor.authorGharesouran, J
dc.contributor.authorAbdii, A
dc.contributor.authorAlizadeh, H
dc.date.accessioned2018-08-26T05:49:05Z
dc.date.available2018-08-26T05:49:05Z
dc.date.issued2014
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/41239
dc.description.abstractEndometrial cancer is the fourth most common cancer among women in developed countries. Patients with endometrial cancer may benefit from systemic chemotherapy alone or in combination with targeted therapies if the disease is clinically diagnosed prior to spread and metastasis to other organs. The aim of this study was to evaluate the prognostic role of p53 polymorphism and its correlation with tumor grade in human uterine endometrial carcinomas.A total of 75 patients with endometrial carcinomas were studied for possible mutations in exon 4 of the p53 gene using polymerase chain reaction and restricting fragment length polymorphism techniques and sequencing.In recent study, The rate of homozygote genotype of pro/pro or Arg/Arg in high grade group was higher than in comparison with low grade one. In addition samples that were undigested in RFLP, showed mutation in exone 4.Our findings showed that high grade endometrial carcinomas are highly associated with TP53 polymorphisms in comparison with low grades.
dc.language.isoEnglish
dc.relation.ispartofAsian Pacific journal of cancer prevention : APJCP
dc.subjectBase Sequence
dc.subjectEndometrial Neoplasms
dc.subjectFemale
dc.subjectGene Frequency
dc.subjectGenetic Predisposition to Disease
dc.subjectHumans
dc.subjectNeoplasm Grading
dc.subjectPolymerase Chain Reaction
dc.subjectPolymorphism, Restriction Fragment Length
dc.subjectPolymorphism, Single Nucleotide
dc.subjectSequence Analysis, DNA
dc.subjectTumor Suppressor Protein p53
dc.titlePolymorphism of p53 gene codon 72 in endometrial cancer: correlation with tumor grade and histological type.
dc.typearticle
dc.citation.volume15
dc.citation.issue22
dc.citation.spage9603
dc.citation.epage6
dc.citation.indexPubmed


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