Introduction: BRCA-mutated breast cancer cells lack the DNA-repair mechanism homologous recombination that is required for error-free DNA double-strand break (DSB) repair. Homologous recombination deficiency (HRD) may cause hypersensitivity to DNA DSB-inducing agents, such as bifunctional alkylating agents and platinum salts. HRD can be caused by BRCA mutations, and by other mechanisms. To identify HRD, studies have focused on triple-negative (TN) breast cancers as these resemble BRCA1-mutated breast cancer closely and might also share this hypersensitivity. However, ways to identify HRD in non-BRCA-mutated, estrogen receptor (ER)-positive breast cancers have remained elusive. The current study provides evidence that genomic patterns resemb...
To access publisher full text version of this article. Please click on the hyperlink in Additional L...
Purpose: Previously, we developed breast cancer BRCA1-like and BRCA2-like copy-number profile shrunk...
BackgroundBreast cancer has a significant heritable basis, of which ∼60% remains unexplained. Testin...
Introduction: BRCA-mutated breast cancer cells lack the DNA-repair mechanism homologous recombinatio...
Breast cancer cells deficient for BRCA1 are hypersensitive to agents inducing DNA double-strand brea...
Genomic patterns resembling BRCA1- and BRCA2-mutated breast cancers predict benefit of intensified c...
Purpose: Breast cancers in carriers of inactivating mutations of the BRCA1 gene carry a specific DNA...
Inactivating mutations in BRCA1 or BRCA2 confer a large lifetime risk of breast and ovarian cancer. ...
Germline mutations in BRCA1/2 predispose individuals to breast cancer (termed germline-mutated BRCA1...
Item does not contain fulltextBACKGROUND: We have previously reported an array comparative genomic h...
ABSTRACT: BACKGROUND: Basal-like breast cancers (BLBC) are aggressive breast cancers for which, so f...
Tumors with homologous recombination deficiency (HRD), such as BRCA1-associated breast cancers, are ...
Introduction: Triple Negative Breast Cancers (TNBC) represent about 12% to 20% of all breast cancers...
Homologous recombination deficiency (HRD) is a defining characteristic in BRCA-deficient breast tumo...
Background: Platinum-based agents may benefit patients with triple-negative breast cancer (TNBC) who...
To access publisher full text version of this article. Please click on the hyperlink in Additional L...
Purpose: Previously, we developed breast cancer BRCA1-like and BRCA2-like copy-number profile shrunk...
BackgroundBreast cancer has a significant heritable basis, of which ∼60% remains unexplained. Testin...
Introduction: BRCA-mutated breast cancer cells lack the DNA-repair mechanism homologous recombinatio...
Breast cancer cells deficient for BRCA1 are hypersensitive to agents inducing DNA double-strand brea...
Genomic patterns resembling BRCA1- and BRCA2-mutated breast cancers predict benefit of intensified c...
Purpose: Breast cancers in carriers of inactivating mutations of the BRCA1 gene carry a specific DNA...
Inactivating mutations in BRCA1 or BRCA2 confer a large lifetime risk of breast and ovarian cancer. ...
Germline mutations in BRCA1/2 predispose individuals to breast cancer (termed germline-mutated BRCA1...
Item does not contain fulltextBACKGROUND: We have previously reported an array comparative genomic h...
ABSTRACT: BACKGROUND: Basal-like breast cancers (BLBC) are aggressive breast cancers for which, so f...
Tumors with homologous recombination deficiency (HRD), such as BRCA1-associated breast cancers, are ...
Introduction: Triple Negative Breast Cancers (TNBC) represent about 12% to 20% of all breast cancers...
Homologous recombination deficiency (HRD) is a defining characteristic in BRCA-deficient breast tumo...
Background: Platinum-based agents may benefit patients with triple-negative breast cancer (TNBC) who...
To access publisher full text version of this article. Please click on the hyperlink in Additional L...
Purpose: Previously, we developed breast cancer BRCA1-like and BRCA2-like copy-number profile shrunk...
BackgroundBreast cancer has a significant heritable basis, of which ∼60% remains unexplained. Testin...