Association of PIK3CA somatic mutations with clinicopathological parameters in breast cancer
The enzyme phosphatidylinositide-3-kinase (PI3K) regulates cellular proliferation and apoptosis. Somatic mutations in the PIK3CA gene can accelerate these processes and significantly contribute to the development and progression of breast cancer. This study aimed to ascertain the PIK3CA gene mut...
Saved in:
Main Authors: | , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Termedia Publishing House
2024-12-01
|
Series: | Polish Journal of Pathology |
Subjects: | |
Online Access: | https://www.termedia.pl/Association-of-PIK3CA-somatic-mutations-with-clinicopathological-parameters-in-breast-cancer,55,55290,1,1.html |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
_version_ | 1832584722027380736 |
---|---|
author | Gizem Teoman Zeynep Turkmen Usta Zeynep Sagnak Yilmaz Sevdegul Aydin Mungan Ismail Saygin |
author_facet | Gizem Teoman Zeynep Turkmen Usta Zeynep Sagnak Yilmaz Sevdegul Aydin Mungan Ismail Saygin |
author_sort | Gizem Teoman |
collection | DOAJ |
description | The enzyme phosphatidylinositide-3-kinase (PI3K) regulates cellular proliferation and apoptosis. Somatic mutations in the PIK3CA gene can accelerate these processes and significantly contribute to the development and progression of breast cancer. This study aimed to ascertain the PIK3CA gene mutations in breast cancer patients and investigate their correlation with certain clinicopathological characteristics.
We conducted a mutational investigation of the PIK3CA gene using next-generation sequencing (NGS) in a sample of 100 cases of primary breast cancer. We investigated the associations between PIK3CA mutations and clinicopathological characteristics.
Our analysis revealed a mutation rate of 45% in the PIK3CA gene. The mutation frequencies for the three hotspot sites were 33.3% for E545K in exon 10, 26.7% for H1047R in exon 20, and 6.7% for E542K in exon 10. Of the 45 individuals with tumors carrying the PIK3CA mutation, 41 (91.2%) had only one mutation, while 4 (8.8%) had two. Pathogenic PIK3CA mutations were significantly correlated with tumor size ( p = 0.015) and tumor location ( p = 0.017).
Our study results demonstrated a significant association between tumor size, location, and presence of the PIK3CA mutation. We must validate these data in larger sample sizes. |
format | Article |
id | doaj-art-542d625147c549daabf86546edd5dce2 |
institution | Kabale University |
issn | 1233-9687 2084-9869 |
language | English |
publishDate | 2024-12-01 |
publisher | Termedia Publishing House |
record_format | Article |
series | Polish Journal of Pathology |
spelling | doaj-art-542d625147c549daabf86546edd5dce22025-01-27T11:36:31ZengTermedia Publishing HousePolish Journal of Pathology1233-96872084-98692024-12-0175426827310.5114/pjp.2024.14570255290Association of PIK3CA somatic mutations with clinicopathological parameters in breast cancerGizem TeomanZeynep Turkmen UstaZeynep Sagnak YilmazSevdegul Aydin MunganIsmail SayginThe enzyme phosphatidylinositide-3-kinase (PI3K) regulates cellular proliferation and apoptosis. Somatic mutations in the PIK3CA gene can accelerate these processes and significantly contribute to the development and progression of breast cancer. This study aimed to ascertain the PIK3CA gene mutations in breast cancer patients and investigate their correlation with certain clinicopathological characteristics. We conducted a mutational investigation of the PIK3CA gene using next-generation sequencing (NGS) in a sample of 100 cases of primary breast cancer. We investigated the associations between PIK3CA mutations and clinicopathological characteristics. Our analysis revealed a mutation rate of 45% in the PIK3CA gene. The mutation frequencies for the three hotspot sites were 33.3% for E545K in exon 10, 26.7% for H1047R in exon 20, and 6.7% for E542K in exon 10. Of the 45 individuals with tumors carrying the PIK3CA mutation, 41 (91.2%) had only one mutation, while 4 (8.8%) had two. Pathogenic PIK3CA mutations were significantly correlated with tumor size ( p = 0.015) and tumor location ( p = 0.017). Our study results demonstrated a significant association between tumor size, location, and presence of the PIK3CA mutation. We must validate these data in larger sample sizes.https://www.termedia.pl/Association-of-PIK3CA-somatic-mutations-with-clinicopathological-parameters-in-breast-cancer,55,55290,1,1.htmlbreast cancer pik3ca mutations hotspot mutations clinicopathological parameters |
spellingShingle | Gizem Teoman Zeynep Turkmen Usta Zeynep Sagnak Yilmaz Sevdegul Aydin Mungan Ismail Saygin Association of PIK3CA somatic mutations with clinicopathological parameters in breast cancer Polish Journal of Pathology breast cancer pik3ca mutations hotspot mutations clinicopathological parameters |
title | Association of PIK3CA somatic mutations with clinicopathological parameters in breast cancer |
title_full | Association of PIK3CA somatic mutations with clinicopathological parameters in breast cancer |
title_fullStr | Association of PIK3CA somatic mutations with clinicopathological parameters in breast cancer |
title_full_unstemmed | Association of PIK3CA somatic mutations with clinicopathological parameters in breast cancer |
title_short | Association of PIK3CA somatic mutations with clinicopathological parameters in breast cancer |
title_sort | association of pik3ca somatic mutations with clinicopathological parameters in breast cancer |
topic | breast cancer pik3ca mutations hotspot mutations clinicopathological parameters |
url | https://www.termedia.pl/Association-of-PIK3CA-somatic-mutations-with-clinicopathological-parameters-in-breast-cancer,55,55290,1,1.html |
work_keys_str_mv | AT gizemteoman associationofpik3casomaticmutationswithclinicopathologicalparametersinbreastcancer AT zeynepturkmenusta associationofpik3casomaticmutationswithclinicopathologicalparametersinbreastcancer AT zeynepsagnakyilmaz associationofpik3casomaticmutationswithclinicopathologicalparametersinbreastcancer AT sevdegulaydinmungan associationofpik3casomaticmutationswithclinicopathologicalparametersinbreastcancer AT ismailsaygin associationofpik3casomaticmutationswithclinicopathologicalparametersinbreastcancer |