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AKT1E17K mutation profiling in breast cancer: prevalence, concurrent oncogenic alterations, and blood-based detection
by
Anzeneder, Tobias
, Schulz, Anke
, Politz, Oliver
, Pena, Carol
, Rudolph, Marion
, Vonk, Richardus
, Köchert, Karl
, Byrne, Annette T.
, Jeffers, Michael
, Beckmann, Georg
, Reischl, Joachim
in
Biomedical and Life Sciences
/ Biomedicine
/ Breast cancer
/ Cancer Research
/ Care and treatment
/ Complications and side effects
/ Diagnosis
/ Gene mutations
/ Genetics
/ genomics and epigenetics
/ Health aspects
/ Health Promotion and Disease Prevention
/ Medicine/Public Health
/ Menopause
/ Metastasis
/ Oncology
/ Research Article
/ Surgical Oncology
2016
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AKT1E17K mutation profiling in breast cancer: prevalence, concurrent oncogenic alterations, and blood-based detection
by
Anzeneder, Tobias
, Schulz, Anke
, Politz, Oliver
, Pena, Carol
, Rudolph, Marion
, Vonk, Richardus
, Köchert, Karl
, Byrne, Annette T.
, Jeffers, Michael
, Beckmann, Georg
, Reischl, Joachim
in
Biomedical and Life Sciences
/ Biomedicine
/ Breast cancer
/ Cancer Research
/ Care and treatment
/ Complications and side effects
/ Diagnosis
/ Gene mutations
/ Genetics
/ genomics and epigenetics
/ Health aspects
/ Health Promotion and Disease Prevention
/ Medicine/Public Health
/ Menopause
/ Metastasis
/ Oncology
/ Research Article
/ Surgical Oncology
2016
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AKT1E17K mutation profiling in breast cancer: prevalence, concurrent oncogenic alterations, and blood-based detection
by
Anzeneder, Tobias
, Schulz, Anke
, Politz, Oliver
, Pena, Carol
, Rudolph, Marion
, Vonk, Richardus
, Köchert, Karl
, Byrne, Annette T.
, Jeffers, Michael
, Beckmann, Georg
, Reischl, Joachim
in
Biomedical and Life Sciences
/ Biomedicine
/ Breast cancer
/ Cancer Research
/ Care and treatment
/ Complications and side effects
/ Diagnosis
/ Gene mutations
/ Genetics
/ genomics and epigenetics
/ Health aspects
/ Health Promotion and Disease Prevention
/ Medicine/Public Health
/ Menopause
/ Metastasis
/ Oncology
/ Research Article
/ Surgical Oncology
2016
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AKT1E17K mutation profiling in breast cancer: prevalence, concurrent oncogenic alterations, and blood-based detection
Journal Article
AKT1E17K mutation profiling in breast cancer: prevalence, concurrent oncogenic alterations, and blood-based detection
2016
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Overview
Background
The single hotspot mutation
AKT1
[G49A:E17K] has been described in several cancers, with the highest incidence observed in breast cancer. However, its precise role in disease etiology remains unknown.
Methods
We analyzed more than 600 breast cancer tumor samples and circulating tumor DNA for
AKT1
E17K
and alterations in other cancer-associated genes using Beads, Emulsions, Amplification, and Magnetics digital polymerase chain reaction technology and targeted exome sequencing.
Results
Overall
AKT1
E17K
mutation prevalence was 6.3 % and not correlated with age or menopausal stage.
AKT1
E17K
mutation frequency tended to be lower in patients with grade 3 disease (1.9 %) compared with those with grade 1 (11.1 %) or grade 2 (6 %) disease. In two cohorts of patients with advanced metastatic disease, 98.0 % (
n =
50) and 97.1 % (
n =
35) concordance was obtained between tissue and blood samples for the
AKT1
E17K
mutation, and mutation capture rates of 66.7 % (2/3) and 85.7 % (6/7) in blood versus tissue samples were observed. Although
AKT1
-mutant tumor specimens were often found to harbor concurrent alterations in other driver genes, a subset of specimens harboring
AKT1
E17K
as the only known driver alteration was also identified. Initial follow-up survival data suggest that
AKT1
E17K
could be associated with increased mortality. These findings warrant additional long-term follow-up.
Conclusions
The data suggest that
AKT1
E17K
is the most likely disease driver in certain breast cancer patients. Blood-based mutation detection is achievable in advanced-stage disease. These findings underpin the need for a further enhanced-precision medicine paradigm in the treatment of breast cancer.
Publisher
BioMed Central,BioMed Central Ltd
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