Cytotoxic and targeted therapy for hereditary cancers

AG Iyevleva, EN Imyanitov - Hereditary cancer in clinical practice, 2016 - Springer
There is a number of drugs demonstrating specific activity towards hereditary cancers. For
example, tumors in BRCA1/2 mutation carriers usually arise via somatic inactivation of the …

[HTML][HTML] Prognostic significance of germline BRCA mutations in patients with HER2-POSITIVE breast cancer

A Viansone, B Pellegrino, C Omarini, M Pistelli… - The Breast, 2022 - Elsevier
Background HER2-positive breast cancers are rare amongst BRCA mutation carriers. No
data exist regarding clinicopathological characteristics and prognosis of this subgroup of …

Prognostic and Predictive Biomarkers in Familial Breast Cancer

S Deb, A Chakrabarti, SB Fox - Cancers, 2023 - mdpi.com
Simple Summary The importance of identifying and targeting in treating familial breast
cancers is becoming increasingly recognized, in particular with increased availability of …

Low prevalence of HER2 positivity amongst BRCA1 and BRCA2 mutation carriers and in primary BRCA screens

DG Evans, F Lalloo, S Howell, S Verhoef… - Breast cancer research …, 2016 - Springer
The aim of this study is to delineate more clearly the prevalence of HER2+ breast cancer in
women with germline BRCA1/2 mutations. For this purpose, we analysed primary mutation …

Case report series: Aggressive HR deficient colorectal cancers related to BRCA1 pathogenic germline variants

MV Freire, M Martin, R Thissen, C Van Marcke… - Frontiers in …, 2022 - frontiersin.org
Objective The link between BRCA1 and homologous recombination deficiency (HRD) in
cancer has gained importance with the emergence of new targeted cancer treatments, while …

Value of the loss of heterozygosity to BRCA1 variant classification

E Santana dos Santos, AB Spurdle, DM Carraro… - NPJ Breast …, 2022 - nature.com
At least 10% of the BRCA1/2 tests identify variants of uncertain significance (VUS) while the
distinction between pathogenic variants (PV) and benign variants (BV) remains particularly …

Identification of CSNK1D and KLK6 as two common upregulated genes present in BRCA1 mutated triple-negative breast cancer and ovarian epithelial carcinoma

F Lakis, R Ayoub, WH Faour, M Makki… - … Nucleotides & Nucleic …, 2024 - Taylor & Francis
Deficiency in the breast cancer type 1 (BRCA1) gene expression predisposes to triple-
negative breast cancer (TNBC) and ovarian cancer (OC). We previously identified by …

Value of the loss of heterozygosity to BRCA1 variant classification

S dos Santos Elizabeth, AB Spurdle… - NPJ Breast …, 2022 - search.proquest.com
At least 10% of the BRCA1/2 tests identify variants of uncertain significance (VUS) while the
distinction between pathogenic variants (PV) and benign variants (BV) remains particularly …

[HTML][HTML] Investigating of variations in BRCA1 gene in Iranian families with breast cancer

A Mehrgou, M Akouchekian… - Medical Journal of the …, 2018 - ncbi.nlm.nih.gov
Background: Breast cancer is one of the most common cancers among Iranian women
whose relationship with mutation status in BRCA1 is previously approved. Therefore …

Contribuição das variantes missense e não codificantes dos gener BRCA1/2 para a predisposição hereditária e resposta ao tratamento dos cânceres de mama e …

ES Santos - 2020 - teses.usp.br
O câncer de mama e de ovário são atualmente definidos de acordo com as principais vias
envolvidas na tumorigênese. Nos cânceres de mama/ovário hereditários (HBOC), os …