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Compromised BRCA1-PALB2 interaction is associated with breast cancer risk

Foo, T K ; Tischkowitz, M ; Simhadri, S ; Boshari, T ; Zayed, N ; Burke, K A ; Berman, S H ; Blecua, P ; Riaz, N ; Huo, Y ; Ding, Y C ; Neuhausen, S L ; Weigelt, B ; Reis-Filho, J S ; Foulkes, W D ; Xia, B

Oncogene, 2017-07, Vol.36 (29), p.4161-4170 [Revista revisada por pares]

England: Nature Publishing Group

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Compromised BRCA1-PALB2 interaction is associated with breast cancer risk
Autor: Foo, T K ; Tischkowitz, M ; Simhadri, S ; Boshari, T ; Zayed, N ; Burke, K A ; Berman, S H ; Blecua, P ; Riaz, N ; Huo, Y ; Ding, Y C ; Neuhausen, S L ; Weigelt, B ; Reis-Filho, J S ; Foulkes, W D ; Xia, B
Materias: Amino Acid Sequence ; BRCA mutations ; BRCA1 protein ; BRCA1 Protein - genetics ; BRCA1 Protein - metabolism ; BRCA2 protein ; Breast cancer ; Breast Neoplasms - genetics ; Breast Neoplasms - metabolism ; Breast Neoplasms - pathology ; Cancer genetics ; Care and treatment ; Cell Line, Tumor ; Deoxyribonucleic acid ; Diagnosis ; DNA ; DNA repair ; Fanconi Anemia Complementation Group N Protein ; Female ; Genetic aspects ; Genetic Predisposition to Disease ; Health aspects ; Health risk assessment ; Homologous recombination ; Humans ; Missense mutation ; Mutation ; Mutation, Missense ; Nuclear Proteins - genetics ; Nuclear Proteins - metabolism ; Pathogenicity ; Patient outcomes ; Platinum ; Poly(ADP-ribose) polymerase ; Protein Binding ; Proteins ; Risk ; Risk factors ; Salts ; Transfection ; Tumor suppressor genes ; Tumor Suppressor Proteins - genetics ; Tumor Suppressor Proteins - metabolism ; Tumors
Es parte de: Oncogene, 2017-07, Vol.36 (29), p.4161-4170
Notas: ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
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Descripción: The major breast cancer suppressor proteins BRCA1 and BRCA2 play essential roles in homologous recombination (HR)-mediated DNA repair, which is thought to be critical for tumor suppression. The two BRCA proteins are linked by a third tumor suppressor, PALB2, in the HR pathway. While truncating mutations in these genes are generally pathogenic, interpretation of missense variants remains a challenge. To date, patient-derived missense variants that disrupt PALB2 binding have been identified in BRCA1 and BRCA2; however, there has not been sufficient evidence to prove their pathogenicity in humans, and no variants in PALB2 that disrupt either its BRCA1 or BRCA2 binding have been reported. Here we report on the identification of a novel PALB2 variant, c.104T>C (p.L35P), that segregates in a family with a strong history of breast cancer. Functional analyses showed that L35P abrogates the PALB2-BRCA1 interaction and completely disables its abilities to promote HR and confer resistance to platinum salts and PARP inhibitors. Whole-exome sequencing of a breast cancer from a c.104T>C carrier revealed a second, somatic, truncating mutation affecting PALB2, and the tumor displays hallmark genomic features of tumors with BRCA mutations and HR defects, cementing the pathogenicity of L35P. Parallel analyses of other germline variants in the PALB2 N-terminal BRCA1-binding domain identified multiple variants that affect HR function to varying degrees, suggesting their possible contribution to cancer development. Our findings establish L35P as the first pathogenic missense mutation in PALB2 and directly demonstrate the requirement of the PALB2-BRCA1 interaction for breast cancer suppression.
Editor: England: Nature Publishing Group
Idioma: Inglés

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Compromised BRCA1-PALB2 interaction is associated with breast cancer risk

Foo, T K ; Tischkowitz, M ; Simhadri, S ; Boshari, T ; Zayed, N ; Burke, K A ; Berman, S H ; Blecua, P ; Riaz, N ; Huo, Y ; Ding, Y C ; Neuhausen, S L ; Weigelt, B ; Reis-Filho, J S ; Foulkes, W D ; Xia, B

England: Nature Publishing Group

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