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PIK3CA Mutation Analysis in Iranian Patients with Gastric Cancer

BACKGROUND: Aberrant activation of phosphatidylinositol-3 kinases (PI3K)/AKT/mTOR (mammalian target of rapamycin) pathway is a critical event during gastric cancer progression. Selective function of AKT inhibitor AZD5363 in PI3KCA mutant gastric cancer necessitates the assessment of PI3KCA mutations...

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Autores principales: Iranpour, Mostafa, Nourian, Mahyar, Saffari, Sana, Samizadeh, Esmaeil, Mirghafori, Mahdieh, Iravani, Shahrokh, Ghafouri-Fard, Soudeh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pasteur Institute 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305827/
https://www.ncbi.nlm.nih.gov/pubmed/29704890
http://dx.doi.org/10.29252/.23.1.87
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author Iranpour, Mostafa
Nourian, Mahyar
Saffari, Sana
Samizadeh, Esmaeil
Mirghafori, Mahdieh
Iravani, Shahrokh
Ghafouri-Fard, Soudeh
author_facet Iranpour, Mostafa
Nourian, Mahyar
Saffari, Sana
Samizadeh, Esmaeil
Mirghafori, Mahdieh
Iravani, Shahrokh
Ghafouri-Fard, Soudeh
author_sort Iranpour, Mostafa
collection PubMed
description BACKGROUND: Aberrant activation of phosphatidylinositol-3 kinases (PI3K)/AKT/mTOR (mammalian target of rapamycin) pathway is a critical event during gastric cancer progression. Selective function of AKT inhibitor AZD5363 in PI3KCA mutant gastric cancer necessitates the assessment of PI3KCA mutations in these patients. METHODS: The study included 100 patients with gastric cancer who underwent surgical resection at Imam Reza Hospital, Tehran, Iran, between January 2009 and December 2016. Mutations in codon 1047 of PIK3CA were evaluated by tetra-primer ARMS-PCR and direct sequencing methods. RESULTS: We detected p.H1047R and p.H1047L in eight and three samples, respectively. Also, a significant association was found between PIK3CA mutations and lymphatic invasion. Kaplan-Meier analysis demonstrated no significant differences in overall survival between patients with and without mutations. CONCLUSION: Our study detected gain-of-function mutations in exon 20 of PI3KCA gene in 11% of gastric cancer patients. Future studies are needed to assess the mutation rate in other regions of this gene to find eligible patients for targeted therapies.
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spelling pubmed-63058272019-01-10 PIK3CA Mutation Analysis in Iranian Patients with Gastric Cancer Iranpour, Mostafa Nourian, Mahyar Saffari, Sana Samizadeh, Esmaeil Mirghafori, Mahdieh Iravani, Shahrokh Ghafouri-Fard, Soudeh Iran Biomed J Short Communication BACKGROUND: Aberrant activation of phosphatidylinositol-3 kinases (PI3K)/AKT/mTOR (mammalian target of rapamycin) pathway is a critical event during gastric cancer progression. Selective function of AKT inhibitor AZD5363 in PI3KCA mutant gastric cancer necessitates the assessment of PI3KCA mutations in these patients. METHODS: The study included 100 patients with gastric cancer who underwent surgical resection at Imam Reza Hospital, Tehran, Iran, between January 2009 and December 2016. Mutations in codon 1047 of PIK3CA were evaluated by tetra-primer ARMS-PCR and direct sequencing methods. RESULTS: We detected p.H1047R and p.H1047L in eight and three samples, respectively. Also, a significant association was found between PIK3CA mutations and lymphatic invasion. Kaplan-Meier analysis demonstrated no significant differences in overall survival between patients with and without mutations. CONCLUSION: Our study detected gain-of-function mutations in exon 20 of PI3KCA gene in 11% of gastric cancer patients. Future studies are needed to assess the mutation rate in other regions of this gene to find eligible patients for targeted therapies. Pasteur Institute 2019-01 /pmc/articles/PMC6305827/ /pubmed/29704890 http://dx.doi.org/10.29252/.23.1.87 Text en Copyright: © Iranian Biomedical Journal http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communication
Iranpour, Mostafa
Nourian, Mahyar
Saffari, Sana
Samizadeh, Esmaeil
Mirghafori, Mahdieh
Iravani, Shahrokh
Ghafouri-Fard, Soudeh
PIK3CA Mutation Analysis in Iranian Patients with Gastric Cancer
title PIK3CA Mutation Analysis in Iranian Patients with Gastric Cancer
title_full PIK3CA Mutation Analysis in Iranian Patients with Gastric Cancer
title_fullStr PIK3CA Mutation Analysis in Iranian Patients with Gastric Cancer
title_full_unstemmed PIK3CA Mutation Analysis in Iranian Patients with Gastric Cancer
title_short PIK3CA Mutation Analysis in Iranian Patients with Gastric Cancer
title_sort pik3ca mutation analysis in iranian patients with gastric cancer
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305827/
https://www.ncbi.nlm.nih.gov/pubmed/29704890
http://dx.doi.org/10.29252/.23.1.87
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