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Effect of p53 codon 72 polymorphism on the survival outcome in advanced stage cervical cancer patients in India
BACKGROUND & OBJECTIVES: The Arg>Pro polymorphism in codon 72 of p53 gene is known to affect the susceptibility of cervical cancer differently in different population worldwide although information regarding its role in determining survival status and disease outcome in patients is lacking. T...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5320841/ https://www.ncbi.nlm.nih.gov/pubmed/28139534 http://dx.doi.org/10.4103/0971-5916.198685 |
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author | Bansal, Akanksha Das, Poulami Kannan, Sadhana Mahantshetty, Umesh Mulherkar, Rita |
author_facet | Bansal, Akanksha Das, Poulami Kannan, Sadhana Mahantshetty, Umesh Mulherkar, Rita |
author_sort | Bansal, Akanksha |
collection | PubMed |
description | BACKGROUND & OBJECTIVES: The Arg>Pro polymorphism in codon 72 of p53 gene is known to affect the susceptibility of cervical cancer differently in different population worldwide although information regarding its role in determining survival status and disease outcome in patients is lacking. The present study was conducted to determine the genotype frequency and prognostic role of p53 codon 72 Arg>Pro polymorphism in patients with advanced stage cervical cancer in India. METHODS: The p53 codon 72 polymorphism was determined in tumour biopsies (n = 107) and matched blood samples (n = 19) in cervical cancer patients using polymerase chain reaction-restriction fragment length polymorphism method (PCR-RFLP). Effect of p53 genotype on the overall survival (OS) and recurrence-free survival (RFS) was analyzed. Individual Arg or Pro alleles were studied for their significance on survival as Pro carriers (Pro/Pro + Arg/Pro) versus Arg/Arg individuals or Arg carriers (Arg/Arg + Arg/Pro) versus Pro/Pro individuals. RESULTS: The frequencies for Arg/Arg, Arg/Pro and Pro/Pro genotypes were 27.2, 49.5 and 23.3 per cent, respectively. There was no significant difference in the genotypes with respect to patients’ OS or RFS. INTERPRETATION & CONCLUSIONS: The findings of our study indicated that p53 codon 72 polymorphism might not be an independent marker in predicting clinical outcome in advanced stage cervical cancer patients. Further studies need to be done in larger samples to confirm these findings. |
format | Online Article Text |
id | pubmed-5320841 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-53208412017-03-01 Effect of p53 codon 72 polymorphism on the survival outcome in advanced stage cervical cancer patients in India Bansal, Akanksha Das, Poulami Kannan, Sadhana Mahantshetty, Umesh Mulherkar, Rita Indian J Med Res Original Article BACKGROUND & OBJECTIVES: The Arg>Pro polymorphism in codon 72 of p53 gene is known to affect the susceptibility of cervical cancer differently in different population worldwide although information regarding its role in determining survival status and disease outcome in patients is lacking. The present study was conducted to determine the genotype frequency and prognostic role of p53 codon 72 Arg>Pro polymorphism in patients with advanced stage cervical cancer in India. METHODS: The p53 codon 72 polymorphism was determined in tumour biopsies (n = 107) and matched blood samples (n = 19) in cervical cancer patients using polymerase chain reaction-restriction fragment length polymorphism method (PCR-RFLP). Effect of p53 genotype on the overall survival (OS) and recurrence-free survival (RFS) was analyzed. Individual Arg or Pro alleles were studied for their significance on survival as Pro carriers (Pro/Pro + Arg/Pro) versus Arg/Arg individuals or Arg carriers (Arg/Arg + Arg/Pro) versus Pro/Pro individuals. RESULTS: The frequencies for Arg/Arg, Arg/Pro and Pro/Pro genotypes were 27.2, 49.5 and 23.3 per cent, respectively. There was no significant difference in the genotypes with respect to patients’ OS or RFS. INTERPRETATION & CONCLUSIONS: The findings of our study indicated that p53 codon 72 polymorphism might not be an independent marker in predicting clinical outcome in advanced stage cervical cancer patients. Further studies need to be done in larger samples to confirm these findings. Medknow Publications & Media Pvt Ltd 2016-09 /pmc/articles/PMC5320841/ /pubmed/28139534 http://dx.doi.org/10.4103/0971-5916.198685 Text en Copyright: © 2017 Indian Journal of Medical Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution NonCommercial ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Bansal, Akanksha Das, Poulami Kannan, Sadhana Mahantshetty, Umesh Mulherkar, Rita Effect of p53 codon 72 polymorphism on the survival outcome in advanced stage cervical cancer patients in India |
title | Effect of p53 codon 72 polymorphism on the survival outcome in advanced stage cervical cancer patients in India |
title_full | Effect of p53 codon 72 polymorphism on the survival outcome in advanced stage cervical cancer patients in India |
title_fullStr | Effect of p53 codon 72 polymorphism on the survival outcome in advanced stage cervical cancer patients in India |
title_full_unstemmed | Effect of p53 codon 72 polymorphism on the survival outcome in advanced stage cervical cancer patients in India |
title_short | Effect of p53 codon 72 polymorphism on the survival outcome in advanced stage cervical cancer patients in India |
title_sort | effect of p53 codon 72 polymorphism on the survival outcome in advanced stage cervical cancer patients in india |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5320841/ https://www.ncbi.nlm.nih.gov/pubmed/28139534 http://dx.doi.org/10.4103/0971-5916.198685 |
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