Germline and Somatic mutations in postmenopausal breast cancer patients

被引:8
|
作者
Nagy, Tauana Rodrigues [1 ]
Maistro, Simone [1 ]
Encinas, Giselly [1 ]
Hirata Katayama, Maria Lucia [1 ]
de Lima Pereira, Glaucia Fernanda [1 ]
Gaburo-Junior, Nelson [2 ]
Moyses Franco, Lucas Augusto [3 ]
Ribeiro Chaves de Gouvea, Ana Carolina [1 ]
Estevez Diz, Maria del Pilar [1 ]
Senna Leite, Luiz Antonio [1 ]
Azevedo Koike Folgueira, Maria Aparecida [1 ]
机构
[1] Univ Sao Paulo, Hosp Clin HCFMUSP, Fac Med, Dept Radiol & Oncol,Inst Canc Estado Sao Paulo IC, Sao Paulo, SP, Brazil
[2] Diagnost Brasil, DB Mol, Sao Paulo, SP, Brazil
[3] Univ Sao Paulo, Fac Med FMUSP, Dept Molestias Infecciosas & Parasitarias, Sao Paulo, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
Breast Cancer; Germline Mutation; Somatic Mutation; BRCA1; BRCA2; PIK3CA; PIK3CA GENE-MUTATIONS; OVARIAN-CANCER; SUSCEPTIBILITY GENES; HEREDITARY BREAST; SEQUENCE VARIANTS; BRCA1; PROGNOSIS; WOMEN; RECOMMENDATIONS; INDIVIDUALS;
D O I
10.6061/clinics/2021/e2837
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVES: In breast cancer (BC) patients, the frequency of germline BRCA mutations (gBRCA) may vary according to the ethnic background, age, and family history of cancer. Phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha (PIK3CA) is the second most common somatic mutated gene in BC; however, the association of mutations in both genes with cancer has not been thoroughly investigated. Thus, our aims were to investigate gBRCA mutation frequency in a cohort of postmenopausal Brazilian BC patients and the association of gBRCA1/BRCA2 and PIK3CA somatic mutations. METHODS: Forty-nine postmenopausal (>55 years) and forty-one young (<= 35 years) BC patients were included in this study. The postmenopausal group included patients who reported a positive family history of cancer. For these patients, gBRCA1/BRCA2 were sequenced using next-generation sequencing (NGS) or Sanger sequencing. Data for gBRCA in young patients were already available from a previous study. DNA from formalin-fixed, paraffin-embedded (FFPE) tumors was obtained from 27 postmenopausal and 41 young patients for analyzing exons 9 and 20 of PIK3CA. The association between gBRCA1/BRCA2 and somatic mutations in PIK3CA was investigated. RESULTS: The overall frequency of gBRCA1/BRCA2 among the 49 postmenopausal patients was 10.2%. The frequencies of somatic mutations in PIK3CA in the postmenopausal and young patients were 37% and 17%, respectively (ns). The most common PIK3CA mutation was found to be E454A. Nonsense and frameshift mutations, which may counteract the oncogenic potential of PIK3CA were also detected. Regardless of age, 25% of BRCA1/BRCA2 mutation carriers and non-carriers , each, had PIK3CA somatic mutations. CONCLUSIONS: Data obtained indicate that BRCA1/BRCA2 gene testing may be considered for postmenopausal patients with BC who have a family history of cancer. Although some of them are not considered pathogenic, somatic variants of PIK3CA are frequently observed in BC patients, especially in postmenopausal patients.
引用
收藏
页数:23
相关论文
共 50 条
  • [1] Somatic and germline mutations of Chinese gastric cancer patients
    Wang, Y.
    Gu, W.
    Zhang, Y.
    Li, K.
    Niu, Z.
    Zheng, Y.
    Cui, Q.
    Wang, A.
    Chen, H.
    Shi, W.
    Wang, K.
    Yao, M.
    [J]. ANNALS OF ONCOLOGY, 2018, 29
  • [2] Comprehensive analysis of the prevalence of germline mutations and their association with somatic mutations in Chinese unselected breast cancer patients
    Liao, Ning
    Chen, Bo
    Zhang, Guochun
    Ren, Chongyang
    Wang, Yulei
    Guo, Liping
    Cao, Li
    Wen, Lingzhu
    Li, Kai
    Jia, Minghan
    Li, Cheukfai
    Mok, Hsiaopei
    Wei, Guangnan
    Lin, Jiali
    Zhang, Zhou
    Hou, Ting
    Lizaso, Analyn
    Liu, Jing
    [J]. CANCER RESEARCH, 2020, 80 (04)
  • [3] Germline and Somatic Mutations in Archived Breast Cancer Specimens of Different Subtypes
    I. S. Abramov
    Yu. S. Korneva
    O. A. Shisterova
    A. Yu. Ikonnikova
    M. A. Emelyanova
    T. S. Lisitsa
    G. S. Krasnov
    T. V. Nasedkina
    [J]. Molecular Biology, 2021, 55 : 354 - 362
  • [4] Germline and Somatic Mutations in Archived Breast Cancer Specimens of Different Subtypes
    Abramov, I. S.
    Korneva, Yu S.
    Shisterova, O. A.
    Ikonnikova, A. Yu
    Emelyanova, M. A.
    Lisitsa, T. S.
    Krasnov, G. S.
    Nasedkina, T., V
    [J]. MOLECULAR BIOLOGY, 2021, 55 (03) : 354 - 362
  • [5] No germline FH mutations in familial breast cancer patients
    Kiuru, M
    Lehtonen, R
    Eerola, H
    Aittomäki, K
    Blomqvist, C
    Nevanlinna, H
    Aaltonen, LA
    Launonen, V
    [J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2005, 13 (04) : 506 - 509
  • [6] No germline FH mutations in familial breast cancer patients
    Maija Kiuru
    Rainer Lehtonen
    Hannaleena Eerola
    Kristiina Aittomäki
    Carl Blomqvist
    Heli Nevanlinna
    Lauri A Aaltonen
    Virpi Launonen
    [J]. European Journal of Human Genetics, 2005, 13 : 506 - 509
  • [7] Somatic mutations and germline sequence variants in patients with familial colorectal cancer
    Gylfe, Alexandra E.
    Sirkia, Johanna
    Ahlsten, Manuel
    Jarvinen, Heikki
    Mecklin, Jukka-Pekka
    Karhu, Auli
    Aaltonen, Lauri A.
    [J]. INTERNATIONAL JOURNAL OF CANCER, 2010, 127 (12) : 2974 - 2980
  • [8] Germline and Somatic Mutations in Prostate Cancer for the Clinician
    Cheng, Heather H.
    Sokolova, Alexandra O.
    Schaeffer, Edward M.
    Small, Eric J.
    Higano, Celestia S.
    [J]. JOURNAL OF THE NATIONAL COMPREHENSIVE CANCER NETWORK, 2019, 17 (05): : 515 - 521
  • [9] MET in human cancer: germline and somatic mutations
    Tovar, Elizabeth A.
    Graveel, Carrie R.
    [J]. ANNALS OF TRANSLATIONAL MEDICINE, 2017, 5 (10)
  • [10] Revealing tumor heterogeneity of breast cancer by utilizing the linkage between somatic and germline mutations
    Zou, Meng
    Jin, Rui
    Au, Kin Fai
    [J]. BRIEFINGS IN BIOINFORMATICS, 2019, 20 (06) : 2306 - 2315