Hereditary Susceptibility for Triple Negative Breast Cancer Associated With Western Sub-Saharan African Ancestry: Results From an International Surgical Breast Cancer Collaborative.


Journal

Annals of surgery
ISSN: 1528-1140
Titre abrégé: Ann Surg
Pays: United States
ID NLM: 0372354

Informations de publication

Date de publication:
09 2019
Historique:
pubmed: 30 7 2019
medline: 13 3 2020
entrez: 30 7 2019
Statut: ppublish

Résumé

To investigate subtype-specific risk of germline alleles associated with triple negative breast cancer (TNBC) in African ancestry populations. Breast cancer (BC) mortality is higher in African American (AA) compared to White American (WA) women; this disparity is partly explained by 2-fold higher TNBC incidence. We used a surgically maintained biospecimen cohort of 2884 BC cases. Subsets of the total (760 AA; 962 WA; 910 West African/Ghanaian; 252 East African/Ethiopian) were analyzed for genotypes of candidate alleles. A subset of 417 healthy controls were also genotyped, to measure associations with overall BC risk and TNBC. TNBC frequency was highest in Ghanaian and AA cases (49% and 44% respectively; P < 0.0001) and lowest in Ethiopian and WA cases (17% and 24% respectively; P < 0.0001). TNBC cases had higher West African ancestry than non-TNBC (P < 0.0001). Frequency of the Duffy-null allele (rs2814778; an African ancestral variant adopted under selective pressure as protection against malaria) was associated with TNBC-specific risk (P < 0.0001), quantified West African Ancestry (P < 0.0001) and was more common in AA, Ghanaians, and TNBC cases. Additionally, rs4849887 was significantly associated with overall BC risk, and both rs2363956 and rs13000023 were associated with TNBC-specific risk, although none as strongly as the Duffy-null variant. West African ancestry is strongly correlated with TNBC status, as well as germline variants related to BC risk. The Duffy-null allele was associated with TNBC risk in our cohort.

Sections du résumé

OBJECTIVE
To investigate subtype-specific risk of germline alleles associated with triple negative breast cancer (TNBC) in African ancestry populations.
BACKGROUND
Breast cancer (BC) mortality is higher in African American (AA) compared to White American (WA) women; this disparity is partly explained by 2-fold higher TNBC incidence.
METHODS
We used a surgically maintained biospecimen cohort of 2884 BC cases. Subsets of the total (760 AA; 962 WA; 910 West African/Ghanaian; 252 East African/Ethiopian) were analyzed for genotypes of candidate alleles. A subset of 417 healthy controls were also genotyped, to measure associations with overall BC risk and TNBC.
RESULTS
TNBC frequency was highest in Ghanaian and AA cases (49% and 44% respectively; P < 0.0001) and lowest in Ethiopian and WA cases (17% and 24% respectively; P < 0.0001). TNBC cases had higher West African ancestry than non-TNBC (P < 0.0001). Frequency of the Duffy-null allele (rs2814778; an African ancestral variant adopted under selective pressure as protection against malaria) was associated with TNBC-specific risk (P < 0.0001), quantified West African Ancestry (P < 0.0001) and was more common in AA, Ghanaians, and TNBC cases. Additionally, rs4849887 was significantly associated with overall BC risk, and both rs2363956 and rs13000023 were associated with TNBC-specific risk, although none as strongly as the Duffy-null variant.
CONCLUSIONS
West African ancestry is strongly correlated with TNBC status, as well as germline variants related to BC risk. The Duffy-null allele was associated with TNBC risk in our cohort.

Identifiants

pubmed: 31356281
doi: 10.1097/SLA.0000000000003459
doi:

Substances chimiques

Receptors, Estrogen 0
Receptors, Progesterone 0
Receptor, ErbB-2 EC 2.7.10.1

Types de publication

Comparative Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

484-492

Subventions

Organisme : NIMHD NIH HHS
ID : L60 MD002419
Pays : United States
Organisme : NIMHD NIH HHS
ID : L60 MD011128
Pays : United States

Auteurs

Lisa A Newman (LA)

Weill Cornell Medicine, New York, NY.

Brittany Jenkins (B)

Weill Cornell Medicine, New York, NY.

Yalei Chen (Y)

Henry Ford Cancer Institute, Detroit, MI.

Joseph K Oppong (JK)

Komfo Anokye Teaching Hospital, Kumasi, Ghana.

Ernest Adjei (E)

Komfo Anokye Teaching Hospital, Kumasi, Ghana.

Aisha S Jibril (AS)

St. Paul's Hospital Millenium Medical College, Addis Ababa, Ethiopia.

Syed Hoda (S)

Weill Cornell Medicine, New York, NY.

Esther Cheng (E)

Weill Cornell Medicine, New York, NY.

Dhananjay Chitale (D)

Komfo Anokye Teaching Hospital, Kumasi, Ghana.

Jessica M Bensenhaver (JM)

Komfo Anokye Teaching Hospital, Kumasi, Ghana.

Baffour Awuah (B)

Komfo Anokye Teaching Hospital, Kumasi, Ghana.

Mahteme Bekele (M)

St. Paul's Hospital Millenium Medical College, Addis Ababa, Ethiopia.

Engida Abebe (E)

St. Paul's Hospital Millenium Medical College, Addis Ababa, Ethiopia.

Ishmael Kyei (I)

Komfo Anokye Teaching Hospital, Kumasi, Ghana.

Frances Aitpillah (F)

Komfo Anokye Teaching Hospital, Kumasi, Ghana.

Michael Adinku (M)

Komfo Anokye Teaching Hospital, Kumasi, Ghana.

Saul David Nathanson (SD)

Henry Ford Cancer Institute, Detroit, MI.

LaToya Jackson (L)

Henry Ford Cancer Institute, Detroit, MI.

Evelyn Jiagge (E)

University of Michigan, Ann Arbor, MI.

Sofia Merajver (S)

University of Michigan, Ann Arbor, MI.

Lindsay F Petersen (LF)

Henry Ford Cancer Institute, Detroit, MI.

Erica Proctor (E)

Henry Ford Cancer Institute, Detroit, MI.

Kofi K Gyan (KK)

Weill Cornell Medicine, New York, NY.

Rachel Martini (R)

Weill Cornell Medicine, New York, NY.

Rick Kittles (R)

City of Hope Comprehensive Cancer Center, Los Angeles, CA.

Melissa B Davis (MB)

Weill Cornell Medicine, New York, NY.

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