BRCA1 promoter methylation in peripheral blood is associated with the risk of triple-negative breast cancer.


Journal

International journal of cancer
ISSN: 1097-0215
Titre abrégé: Int J Cancer
Pays: United States
ID NLM: 0042124

Informations de publication

Date de publication:
01 03 2020
Historique:
received: 27 05 2019
revised: 19 07 2019
accepted: 16 08 2019
pubmed: 31 8 2019
medline: 15 2 2020
entrez: 31 8 2019
Statut: ppublish

Résumé

Methylation of the promoter of the BRCA1 gene in DNA derived from peripheral blood cells is a possible risk factor for breast cancer. It is not clear if this association is restricted to certain types of breast cancer or is a general phenomenon. We evaluated BRCA1 methylation status in peripheral blood cells from 942 breast cancer patients and from 500 controls. We also assessed methylation status in 262 paraffin-embedded breast cancer tissues. Methylation status was assessed using methylation-sensitive high-resolution melting and was categorized as positive or negative. BRCA1 methylation in peripheral blood cells was strongly associated with the risk of triple-negative breast cancer (TNBC) (odds ratio [OR] 4.70; 95% confidence interval [CI]: 3.13-7.07; p < 0.001), but not of estrogen-receptor positive breast cancer (OR 0.80; 95% CI: 0.46-1.42; p = 0.46). Methylation was also overrepresented among patients with high-grade cancers (OR 4.53; 95% CI: 2.91-7.05; p < 0.001) and medullary cancers (OR 3.08; 95% CI: 1.38-6.88; p = 0.006). Moreover, we detected a significant concordance of BRCA1 promoter methylation in peripheral blood and paired tumor tissue (p < 0.001). We found that BRCA1 promoter methylation in peripheral blood cells is associated with approximately five times greater risk of TNBC. We propose that BRCA1 methylation in blood-derived DNA could be a novel biomarker of increased breast cancer susceptibility, in particular for triple-negative tumors.

Identifiants

pubmed: 31469414
doi: 10.1002/ijc.32655
doi:

Substances chimiques

BRCA1 Protein 0
BRCA1 protein, human 0
Biomarkers, Tumor 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1293-1298

Informations de copyright

© 2019 UICC.

Références

Lubiński J, Górski B, Huzarski T, et al. BRCA1-positive breast cancers in young women from Poland. Breast Cancer Res Treat 2006;99:71-6.
Szwiec M, Jakubowska A, Górski B, et al. Recurrent mutations of BRCA1 and BRCA2 in Poland: an update. Clin Genet 2015;87:288-92.
Clark SL, Rodriguez AM, Snyder RR, et al. Structure-function of the tumor suppressor BRCA1. Comput Struct Biotechnol J 2012;1:e201204005.
Tavtigian SV, Simard J, Rommens J, et al. The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds. Nat Genet 1996;12:333-7.
Wu H, Wu X, Liang Z. Impact of germline and somatic BRCA1/2 mutations: tumor spectrum and detection platforms. Gene Ther 2017;24:601-9.
van Veldhoven K, Polidoro S, Baglietto L, et al. Epigenome-wide association study reveals decreased average methylation levels years before breast cancer diagnosis. Clin Epigenetics 2015;7:67.
Severi G, Southey MC, English DR, et al. Epigenome-wide methylation in DNA from peripheral blood as a marker of risk for breast cancer. Breast Cancer Res Treat 2014;148:665-73.
Wong EM, Southey MC, Fox SB, et al. Constitutional methylation of the BRCA1 promoter is specifically associated with BRCA1 mutation-associated pathology in early onset breast cancer. Cancer Prev Res 2010;4:23-33.
Flanagan JM, Munoz-Alegre M, Henderson S, et al. Gene-body hypermethylation of ATM in peripheral blood DNA of bilateral breast cancer patients. Hum Mol Genet 2009;18:1332-42.
Zhang L, Long X. Association of BRCA1 promoter methylation with sporadic breast cancers: evidence from 40 studies. Sci Rep 2015;5:17869.
Wojdacz TK, Thestrup BB, Overgaard J, et al. Methylation of cancer related genes in tumor and peripheral blood DNA from the same breast cancer patient as two independent events. Diagn Pathol 2011;6:116.
Cho YH, Yazici H, Wu HC, et al. Aberrant promoter hypermethylation and genomic hypomethylation in tumor, adjacent normal tissues and blood from breast cancer patients. Anticancer Res 2010;30:2489-96.
Bosviel R, Garcia S, Lavediaux G, et al. BRCA1 promoter methylation in peripheral blood DNA was identified in sporadic breast cancer and controls. Cancer Epidemiol 2012;36:e177-82.
Iwamoto T, Yamamoto N, Taguchi T, et al. BRCA1 promoter methylation in peripheral blood cells is associated with increased risk of breast cancer with BRCA1 promoter methylation. Breast Cancer Res Treat 2011;129:69-77.
Daniels SL, Burghel GJ, Chambers P, et al. Levels of DNA methylation vary at CpG sites across the BRCA1 promoter, and differ according to triple negative and "BRCA-like" status, in both blood and tumour DNA. PLoS One 2016;11:e0160174.
Gupta S, Jaworska-Bieniek K, Narod SA, et al. Methylation of the BRCA1 promoter in peripheral blood DNA is associated with triple negative and medullary breast cancer. Breast Cancer Res Treat 2014;148:615-22.
Mavaddat N, Barrowdale D, Andrulis IL, et al. Consortium of investigators of modifiers of BRCA1/2. Pathology of breast and ovarian cancers among BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA). Cancer Epidemiol Biomarkers Prev 2012;21:134-47.
Hahnen E, Hauke J, Engel C, et al. Germline mutations in triple-negative breast cancer. Breast Care (Basel) 2017;12:15-9.
Brianese RC, Nakamura KDM, Almeida FGDSR, et al. BRCA1 deficiency is a recurrent event in early-onset triple-negative breast cancer: a comprehensive analysis of germline mutations and somatic promoter methylation. Breast Cancer Res Treat 2018;167:803-14.
Lips EH, Mulder L, Oonk A, et al. Triple-negative breast cancer: BRCAness and concordance of clinical features with BRCA1-mutation carriers. Br J Cancer 2013;108:2172-7.
Górski B, Jakubowska A, Huzarski T, et al. A high proportion of founder BRCA1 mutations in Polish breast cancer families. Int J Cancer 2004;110:683-6.
Cybulski C, Kluźniak W, Huzarski T, et al. The spectrum of mutations predisposing to familial breast cancer in Poland. Int J Cancer 2019. https://doi.org/10.1002/ijc.32492.
Wong-Brown MW, Meldrum CJ, Carpenter JE, et al. Prevalence of BRCA1 and BRCA2 germline mutations in patients with triple-negative breast cancer. Breast Cancer Res Treat 2015;150:71-80.
Lahiri DK, Schnabel B. DNA isolation by a rapid method from human blood samples: effects of MgCl2, EDTA, storage time, and temperature on DNA yield and quality. Biochem Genet 2007;31:321-8.
Wojdacz TK, Dobrovic A, Hansen LL. Methylation-sensitive high-resolution melting. Nat Protoc 2008;3:1903-8.
Wojdacz TK, Møller TH, Thestrup BB, et al. Limitations and advantages of MS-HRM and bisulfite sequencing for single locus methylation studies. Expert Rev Mol Diagn 2010;10:575-80.
Wojdacz TK, Thestrup BB, Cold S, et al. No difference in the frequency of locus-specific methylation in the peripheral blood DNA of women diagnosed with breast cancer and age-matched controls. Future Oncol 2011;7:1451-5.
Górski B, Cybulski C, Huzarski T, et al. Breast cancer predisposing alleles in Poland. Breast Cancer Res Treat 2005;92:19-24.
Ford D, Easton DF, Bishop DT, et al. Risks of cancer in BRCA1-mutation carriers. Breast Cancer Linkage Consortium. Lancet 1994;343:692-5.
Antoniou A, Pharoah PD, Narod S, et al. Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case series unselected for family history: a combined analysis of 22 studies. Am J Hum Genet 2003;72:1117-30.
Rodríguez-Balada M, Roig B, Melé M, et al. Germline promoter hypermethylation in BRCA1 and BRCA2 genes is not present in hereditary breast cancer patients. Clin Transl Oncol 2018;20:1226-31.
Kontorovich T, Cohen Z, Nir U, et al. Promoter methylation patterns of ATM, ATR, BRCA1, BRCA2 and p53 as putative cancer risk modifiers in Jewish BRCA1/BRCA2 mutation carriers. Breast Cancer Res Treat 2009;116:195-200.
Cho YH, McCullough LE, Gammon MD, et al. Promoter hypermethylationin white blood cell DNA and breast cancer risk. J Cancer 2015;6:819-24.
Verhoog LC, Brekelmans CT, Seynaeve C, et al. Survival and tumour characteristics of breast-cancer patients with germline mutations of BRCA1. Lancet 1998;351:316-21.
Huzarski T, Byrski T, Gronwald J, et al. Ten-year survival in patients with BRCA1-negative and BRCA1-positive breast cancer. J Clin Oncol 2013;31:3191-6.
van den Broek AJ, Schmidt MK, van 't Veer LJ, et al. Worse breast cancer prognosis of BRCA1/BRCA2 mutation carriers: what's the evidence? A systematic review with meta-analysis. PLoS One 2015;10:e0120189.

Auteurs

Karolina Prajzendanc (K)

Department of Genetics and Pathology, Pomeranian Medical University, Szczecin, Poland.

Paweł Domagała (P)

Department of Pathology, Pomeranian Medical University, Szczecin, Poland.

Jolanta Hybiak (J)

Department of Pathology, Pomeranian Medical University, Szczecin, Poland.

Janusz Ryś (J)

Department of Tumor Pathology, Maria Skłodowska-Curie Memorial Centre and Institute of Oncology, Cracow, Poland.

Tomasz Huzarski (T)

Department of Genetics and Pathology, Pomeranian Medical University, Szczecin, Poland.
Department of Clinical Genetics and Pathology, University of Zielona Góra, Zielona Góra, Poland.

Marek Szwiec (M)

Department of Surgery and Oncology, University of Zielona Góra, Zielona Góra, Poland.
Department of Clinical Oncology, University Hospital in Zielona Góra, Zielona Góra, Poland.

Joanna Tomiczek-Szwiec (J)

Department of Histology, Institute of Medicine, University of Opole, Opole, Poland.
Regional Oncology Centre, Opole, Poland.

Wojciech Redelbach (W)

Department of Anatomy, Institute of Medicine, University of Opole, Opole, Poland.

Aleksandra Sejda (A)

Department of Pathology, Provincial Specialist Hospital, Olsztyn, Poland.
Patomorphology Department, University of Warmia and Mazury, Olsztyn, Poland.

Jacek Gronwald (J)

Department of Genetics and Pathology, Pomeranian Medical University, Szczecin, Poland.

Tomasz Kluz (T)

Institute of Obstetric and Emergency Medicine, Faculty of Medicine, University of Rzeszow, Rzeszow, Poland.

Rafał Wiśniowski (R)

Department of Clinical Oncology, Regional Oncology Centre, Bielsko-Biala, Poland.

Cezary Cybulski (C)

Department of Genetics and Pathology, Pomeranian Medical University, Szczecin, Poland.

Alicja Łukomska (A)

Department of Genetics and Pathology, Pomeranian Medical University, Szczecin, Poland.

Katarzyna Białkowska (K)

Department of Genetics and Pathology, Pomeranian Medical University, Szczecin, Poland.

Grzegorz Sukiennicki (G)

Department of Genetics and Pathology, Pomeranian Medical University, Szczecin, Poland.

Katarzyna Kulczycka (K)

Department of Genetics and Pathology, Pomeranian Medical University, Szczecin, Poland.

Steven A Narod (SA)

Women's College Research Institute, Women's College Hospital, Toronto, ON, Canada.

Tomasz K Wojdacz (TK)

Independent Clinical Epigenetics Laboratory, Pomeranian Medical University, Szczecin, Poland.

Jan Lubiński (J)

Department of Genetics and Pathology, Pomeranian Medical University, Szczecin, Poland.

Anna Jakubowska (A)

Department of Genetics and Pathology, Pomeranian Medical University, Szczecin, Poland.
Independent Laboratory of Molecular Biology and Genetic Diagnostics, Pomeranian Medical University, Szczecin, Poland.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH