Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers

Paolo Peterlongo; Jenny Chang-Claude; Kirsten B Moysich; Anja Rudolph; Rita K Schmutzler; Jacques Simard; Penny Soucy; Rosalind A Eeles; Douglas F Easton; Ute Hamann; Stefan Wilkening; Bowang Chen; Matti A Rookus; Marjanka K Schmidt; Frederieke H van der Baan; Amanda B Spurdle; Logan C Walker; Felicity Lose; Ana-Teresa Maia; Marco Montagna; Laura Matricardi; Jan Lubinski; Anna Jakubowska; Encarna B Gómez Garcia; Olufunmilayo I Olopade; Robert L Nussbaum; Katherine L Nathanson; Susan M Domchek; Timothy R Rebbeck; Banu K Arun; Beth Y Karlan; Sandra Orsulic; Jenny Lester; Wendy K Chung; Alex Miron; Melissa C Southey; David E Goldgar; Saundra S Buys; Ramunas Janavicius; Cecilia M Dorfling; Elizabeth J van Rensburg; Yuan Chun Ding; Susan L Neuhausen; Thomas v. O. Hansen; Anne-Marie Gerdes; Bent Ejlertsen; Lars Jønson; Ana Osorio; Cristina Martínez-Bouzas; Javier Benitez; EMBRACE

doi:10.1158/1055-9965.epi-14-0532

Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers

Paolo Peterlongo, Jenny Chang-Claude, Kirsten B Moysich, Anja Rudolph, Rita K Schmutzler, Jacques Simard, Penny Soucy, Rosalind A Eeles, Douglas F Easton, Ute Hamann, Stefan Wilkening, Bowang Chen, Matti A Rookus, Marjanka K Schmidt, Frederieke H van der Baan, Amanda B Spurdle, Logan C Walker, Felicity Lose, Ana-Teresa Maia, Marco MontagnaLaura Matricardi, Jan Lubinski, Anna Jakubowska, Encarna B Gómez Garcia, Olufunmilayo I Olopade, Robert L Nussbaum, Katherine L Nathanson, Susan M Domchek, Timothy R Rebbeck, Banu K Arun, Beth Y Karlan, Sandra Orsulic, Jenny Lester, Wendy K Chung, Alex Miron, Melissa C Southey, David E Goldgar, Saundra S Buys, Ramunas Janavicius, Cecilia M Dorfling, Elizabeth J van Rensburg, Yuan Chun Ding, Susan L Neuhausen, Thomas v. O. Hansen, Anne-Marie Gerdes, Bent Ejlertsen, Lars Jønson, Ana Osorio, Cristina Martínez-Bouzas, Javier Benitez, EMBRACE

16 Citationer (Scopus)

Abstract

BACKGROUND: BRCA1 and BRCA2 mutation carriers are at substantially increased risk for developing breast and ovarian cancer. The incomplete penetrance coupled with the variable age at diagnosis in carriers of the same mutation suggests the existence of genetic and nongenetic modifying factors. In this study, we evaluated the putative role of variants in many candidate modifier genes.

METHODS: Genotyping data from 15,252 BRCA1 and 8,211 BRCA2 mutation carriers, for known variants (n = 3,248) located within or around 445 candidate genes, were available through the iCOGS custom-designed array. Breast and ovarian cancer association analysis was performed within a retrospective cohort approach.

RESULTS: The observed P values of association ranged between 0.005 and 1.000. None of the variants was significantly associated with breast or ovarian cancer risk in either BRCA1 or BRCA2 mutation carriers, after multiple testing adjustments.

CONCLUSION: There is little evidence that any of the evaluated candidate variants act as modifiers of breast and/or ovarian cancer risk in BRCA1 or BRCA2 mutation carriers.

IMPACT: Genome-wide association studies have been more successful at identifying genetic modifiers of BRCA1/2 penetrance than candidate gene studies.

Originalsprog	Engelsk
Tidsskrift	Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology
Vol/bind	24
Udgave nummer	1
Sider (fra-til)	308-16
Antal sider	9
ISSN	1055-9965
DOI	https://doi.org/10.1158/1055-9965.epi-14-0532
Status	Udgivet - 1 jan. 2015

FN’s Verdensmål

Dette resultat bidrager til følgende verdensmål

Adgang til dokumentet

10.1158/1055-9965.epi-14-0532

308.full.pdfForlagets udgivne version, 296 KB

Citationsformater

Peterlongo, P., Chang-Claude, J., Moysich, K. B., Rudolph, A., Schmutzler, R. K., Simard, J., Soucy, P., Eeles, R. A., Easton, D. F., Hamann, U., Wilkening, S., Chen, B., Rookus, M. A., Schmidt, M. K., van der Baan, F. H., Spurdle, A. B., Walker, L. C., Lose, F., Maia, A-T., ... EMBRACE (2015). Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 24(1), 308-16. https://doi.org/10.1158/1055-9965.epi-14-0532

Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers. / Peterlongo, Paolo; Chang-Claude, Jenny; Moysich, Kirsten B et al.

I: Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, Bind 24, Nr. 1, 01.01.2015, s. 308-16.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

Peterlongo, P, Chang-Claude, J, Moysich, KB, Rudolph, A, Schmutzler, RK, Simard, J, Soucy, P, Eeles, RA, Easton, DF, Hamann, U, Wilkening, S, Chen, B, Rookus, MA, Schmidt, MK, van der Baan, FH, Spurdle, AB, Walker, LC, Lose, F, Maia, A-T, Montagna, M, Matricardi, L, Lubinski, J, Jakubowska, A, Gómez Garcia, EB, Olopade, OI, Nussbaum, RL, Nathanson, KL, Domchek, SM, Rebbeck, TR, Arun, BK, Karlan, BY, Orsulic, S, Lester, J, Chung, WK, Miron, A, Southey, MC, Goldgar, DE, Buys, SS, Janavicius, R, Dorfling, CM, van Rensburg, EJ, Ding, YC, Neuhausen, SL, Hansen, TVO, Gerdes, A-M, Ejlertsen, B, Jønson, L, Osorio, A, Martínez-Bouzas, C, Benitez, J & EMBRACE 2015, 'Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers', Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, bind 24, nr. 1, s. 308-16. https://doi.org/10.1158/1055-9965.epi-14-0532

Peterlongo P, Chang-Claude J, Moysich KB, Rudolph A, Schmutzler RK, Simard J et al. Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. 2015 jan. 1;24(1):308-16. doi: 10.1158/1055-9965.epi-14-0532

Peterlongo, Paolo ; Chang-Claude, Jenny ; Moysich, Kirsten B et al. / Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers. I: Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. 2015 ; Bind 24, Nr. 1. s. 308-16.

@article{539ad2e8c17b4c41b020564446968ea7,

title = "Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers",

abstract = "BACKGROUND: BRCA1 and BRCA2 mutation carriers are at substantially increased risk for developing breast and ovarian cancer. The incomplete penetrance coupled with the variable age at diagnosis in carriers of the same mutation suggests the existence of genetic and nongenetic modifying factors. In this study, we evaluated the putative role of variants in many candidate modifier genes.METHODS: Genotyping data from 15,252 BRCA1 and 8,211 BRCA2 mutation carriers, for known variants (n = 3,248) located within or around 445 candidate genes, were available through the iCOGS custom-designed array. Breast and ovarian cancer association analysis was performed within a retrospective cohort approach.RESULTS: The observed P values of association ranged between 0.005 and 1.000. None of the variants was significantly associated with breast or ovarian cancer risk in either BRCA1 or BRCA2 mutation carriers, after multiple testing adjustments.CONCLUSION: There is little evidence that any of the evaluated candidate variants act as modifiers of breast and/or ovarian cancer risk in BRCA1 or BRCA2 mutation carriers.IMPACT: Genome-wide association studies have been more successful at identifying genetic modifiers of BRCA1/2 penetrance than candidate gene studies.",

keywords = "Adult, Breast Neoplasms, Cohort Studies, Female, Genes, BRCA1, Genes, BRCA2, Humans, Mutation, Ovarian Neoplasms, Polymorphism, Single Nucleotide, Retrospective Studies, Young Adult",

author = "Paolo Peterlongo and Jenny Chang-Claude and Moysich, {Kirsten B} and Anja Rudolph and Schmutzler, {Rita K} and Jacques Simard and Penny Soucy and Eeles, {Rosalind A} and Easton, {Douglas F} and Ute Hamann and Stefan Wilkening and Bowang Chen and Rookus, {Matti A} and Schmidt, {Marjanka K} and {van der Baan}, {Frederieke H} and Spurdle, {Amanda B} and Walker, {Logan C} and Felicity Lose and Ana-Teresa Maia and Marco Montagna and Laura Matricardi and Jan Lubinski and Anna Jakubowska and {G{\'o}mez Garcia}, {Encarna B} and Olopade, {Olufunmilayo I} and Nussbaum, {Robert L} and Nathanson, {Katherine L} and Domchek, {Susan M} and Rebbeck, {Timothy R} and Arun, {Banu K} and Karlan, {Beth Y} and Sandra Orsulic and Jenny Lester and Chung, {Wendy K} and Alex Miron and Southey, {Melissa C} and Goldgar, {David E} and Buys, {Saundra S} and Ramunas Janavicius and Dorfling, {Cecilia M} and {van Rensburg}, {Elizabeth J} and Ding, {Yuan Chun} and Neuhausen, {Susan L} and Hansen, {Thomas v. O.} and Anne-Marie Gerdes and Bent Ejlertsen and Lars J{\o}nson and Ana Osorio and Cristina Mart{\'i}nez-Bouzas and Javier Benitez and EMBRACE",

note = "{\textcopyright}2014 American Association for Cancer Research.",

year = "2015",

month = jan,

day = "1",

doi = "10.1158/1055-9965.epi-14-0532",

language = "English",

volume = "24",

pages = "308--16",

journal = "Cancer Epidemiology, Biomarkers & Prevention",

issn = "1055-9965",

publisher = "American Association for Cancer Research (A A C R)",

number = "1",

}

TY - JOUR

T1 - Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers

AU - Peterlongo, Paolo

AU - Chang-Claude, Jenny

AU - Moysich, Kirsten B

AU - Rudolph, Anja

AU - Schmutzler, Rita K

AU - Simard, Jacques

AU - Soucy, Penny

AU - Eeles, Rosalind A

AU - Easton, Douglas F

AU - Hamann, Ute

AU - Wilkening, Stefan

AU - Chen, Bowang

AU - Rookus, Matti A

AU - Schmidt, Marjanka K

AU - van der Baan, Frederieke H

AU - Spurdle, Amanda B

AU - Walker, Logan C

AU - Lose, Felicity

AU - Maia, Ana-Teresa

AU - Montagna, Marco

AU - Matricardi, Laura

AU - Lubinski, Jan

AU - Jakubowska, Anna

AU - Gómez Garcia, Encarna B

AU - Olopade, Olufunmilayo I

AU - Nussbaum, Robert L

AU - Nathanson, Katherine L

AU - Domchek, Susan M

AU - Rebbeck, Timothy R

AU - Arun, Banu K

AU - Karlan, Beth Y

AU - Orsulic, Sandra

AU - Lester, Jenny

AU - Chung, Wendy K

AU - Miron, Alex

AU - Southey, Melissa C

AU - Goldgar, David E

AU - Buys, Saundra S

AU - Janavicius, Ramunas

AU - Dorfling, Cecilia M

AU - van Rensburg, Elizabeth J

AU - Ding, Yuan Chun

AU - Neuhausen, Susan L

AU - Hansen, Thomas v. O.

AU - Gerdes, Anne-Marie

AU - Ejlertsen, Bent

AU - Jønson, Lars

AU - Osorio, Ana

AU - Martínez-Bouzas, Cristina

AU - Benitez, Javier

AU - EMBRACE

PY - 2015/1/1

Y1 - 2015/1/1

N2 - BACKGROUND: BRCA1 and BRCA2 mutation carriers are at substantially increased risk for developing breast and ovarian cancer. The incomplete penetrance coupled with the variable age at diagnosis in carriers of the same mutation suggests the existence of genetic and nongenetic modifying factors. In this study, we evaluated the putative role of variants in many candidate modifier genes.METHODS: Genotyping data from 15,252 BRCA1 and 8,211 BRCA2 mutation carriers, for known variants (n = 3,248) located within or around 445 candidate genes, were available through the iCOGS custom-designed array. Breast and ovarian cancer association analysis was performed within a retrospective cohort approach.RESULTS: The observed P values of association ranged between 0.005 and 1.000. None of the variants was significantly associated with breast or ovarian cancer risk in either BRCA1 or BRCA2 mutation carriers, after multiple testing adjustments.CONCLUSION: There is little evidence that any of the evaluated candidate variants act as modifiers of breast and/or ovarian cancer risk in BRCA1 or BRCA2 mutation carriers.IMPACT: Genome-wide association studies have been more successful at identifying genetic modifiers of BRCA1/2 penetrance than candidate gene studies.

AB - BACKGROUND: BRCA1 and BRCA2 mutation carriers are at substantially increased risk for developing breast and ovarian cancer. The incomplete penetrance coupled with the variable age at diagnosis in carriers of the same mutation suggests the existence of genetic and nongenetic modifying factors. In this study, we evaluated the putative role of variants in many candidate modifier genes.METHODS: Genotyping data from 15,252 BRCA1 and 8,211 BRCA2 mutation carriers, for known variants (n = 3,248) located within or around 445 candidate genes, were available through the iCOGS custom-designed array. Breast and ovarian cancer association analysis was performed within a retrospective cohort approach.RESULTS: The observed P values of association ranged between 0.005 and 1.000. None of the variants was significantly associated with breast or ovarian cancer risk in either BRCA1 or BRCA2 mutation carriers, after multiple testing adjustments.CONCLUSION: There is little evidence that any of the evaluated candidate variants act as modifiers of breast and/or ovarian cancer risk in BRCA1 or BRCA2 mutation carriers.IMPACT: Genome-wide association studies have been more successful at identifying genetic modifiers of BRCA1/2 penetrance than candidate gene studies.

KW - Adult

KW - Breast Neoplasms

KW - Cohort Studies

KW - Female

KW - Genes, BRCA1

KW - Genes, BRCA2

KW - Humans

KW - Mutation

KW - Ovarian Neoplasms

KW - Polymorphism, Single Nucleotide

KW - Retrospective Studies

KW - Young Adult

U2 - 10.1158/1055-9965.epi-14-0532

DO - 10.1158/1055-9965.epi-14-0532

M3 - Journal article

C2 - 25336561

SN - 1055-9965

VL - 24

SP - 308

EP - 316

JO - Cancer Epidemiology, Biomarkers & Prevention

JF - Cancer Epidemiology, Biomarkers & Prevention

IS - 1

ER -

Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers

Abstract

FN’s Verdensmål

Adgang til dokumentet

Fingeraftryk

Citationsformater