Genetic predisposition to ductal carcinoma in situ of the breast

Christos Petridis; Mark N Brook; Vandna Shah; Kelly Kohut; Patricia Gorman; Michele Caneppele; Dina Levi; Efterpi Papouli; Nick Orr; Angela Cox; Simon S Cross; Isabel Dos-Santos-Silva; Julian Peto; Anthony Swerdlow; Minouk J Schoemaker; Manjeet K Bolla; Q. Wang; Joe Dennis; Kyriaki Michailidou; Javier Benitez; Anna González-Neira; Daniel C Tessier; Daniel Vincent; Jingmei Li; Jonine Figueroa; Vessela Kristensen; Anne-Lise Borresen-Dale; Penny Soucy; Jacques Simard; Roger L Milne; Graham G Giles; Sara Margolin; Annika Lindblom; Thomas Brüning; Hiltrud Brauch; Melissa C Southey; John L Hopper; Thilo Dörk; Natalia V Bogdanova; Maria Kabisch; Ute Hamann; Rita K Schmutzler; Alfons Meindl; Hermann Brenner; Volker Arndt; Robert Winqvist; Katri Pylkäs; Peter A Fasching; Matthias W Beckmann; Jan Lubinski; Anna Jakubowska; Anna Marie Mulligan; Irene L Andrulis; Rob A E M Tollenaar; Peter Devilee; Loic Le Marchand; Christopher A Haiman; Arto Mannermaa; Veli-Matti Kosma; Paolo Radice; Paolo Peterlongo; Frederik Marme; Barbara Burwinkel; Carolien H M van Deurzen; Antoinette Hollestelle; Nicola Miller; Michael J Kerin; Diether Lambrechts; Giuseppe Floris; Jelle Wesseling; Henrik Flyger; Stig E Bojesen; Song Yao; Christine B Ambrosone; Georgia Chenevix-Trench; Thérèse Truong; Pascal Guénel; Anja Rudolph; Jenny Chang-Claude; Heli Nevanlinna; Carl Blomqvist; Kamila Czene; Judith S Brand; Janet E Olson; Fergus J Couch; Alison M Dunning; Per Hall; Douglas F Easton; Paul D P Pharoah; Sarah E Pinder; Marjanka K Schmidt; Ian Tomlinson; Rebecca Roylance; Montserrat García-Closas; Elinor J Sawyer

doi:10.1186/s13058-016-0675-7

Genetic predisposition to ductal carcinoma in situ of the breast

Christos Petridis, Mark N Brook, Vandna Shah, Kelly Kohut, Patricia Gorman, Michele Caneppele, Dina Levi, Efterpi Papouli, Nick Orr, Angela Cox, Simon S Cross, Isabel Dos-Santos-Silva, Julian Peto, Anthony Swerdlow, Minouk J Schoemaker, Manjeet K Bolla, Q. Wang, Joe Dennis, Kyriaki Michailidou, Javier BenitezAnna González-Neira, Daniel C Tessier, Daniel Vincent, Jingmei Li, Jonine Figueroa, Vessela Kristensen, Anne-Lise Borresen-Dale, Penny Soucy, Jacques Simard, Roger L Milne, Graham G Giles, Sara Margolin, Annika Lindblom, Thomas Brüning, Hiltrud Brauch, Melissa C Southey, John L Hopper, Thilo Dörk, Natalia V Bogdanova, Maria Kabisch, Ute Hamann, Rita K Schmutzler, Alfons Meindl, Hermann Brenner, Volker Arndt, Robert Winqvist, Katri Pylkäs, Peter A Fasching, Matthias W Beckmann, Jan Lubinski, Anna Jakubowska, Anna Marie Mulligan, Irene L Andrulis, Rob A E M Tollenaar, Peter Devilee, Loic Le Marchand, Christopher A Haiman, Arto Mannermaa, Veli-Matti Kosma, Paolo Radice, Paolo Peterlongo, Frederik Marme, Barbara Burwinkel, Carolien H M van Deurzen, Antoinette Hollestelle, Nicola Miller, Michael J Kerin, Diether Lambrechts, Giuseppe Floris, Jelle Wesseling, Henrik Flyger, Stig E Bojesen, Song Yao, Christine B Ambrosone, Georgia Chenevix-Trench, Thérèse Truong, Pascal Guénel, Anja Rudolph, Jenny Chang-Claude, Heli Nevanlinna, Carl Blomqvist, Kamila Czene, Judith S Brand, Janet E Olson, Fergus J Couch, Alison M Dunning, Per Hall, Douglas F Easton, Paul D P Pharoah, Sarah E Pinder, Marjanka K Schmidt, Ian Tomlinson, Rebecca Roylance, Montserrat García-Closas, Elinor J Sawyer

Institut for Klinisk Medicin

30 Citationer (Scopus)

Abstract

Background: Ductal carcinoma in situ (DCIS) is a non-invasive form of breast cancer. It is often associated with invasive ductal carcinoma (IDC), and is considered to be a non-obligate precursor of IDC. It is not clear to what extent these two forms of cancer share low-risk susceptibility loci, or whether there are differences in the strength of association for shared loci. Methods: To identify genetic polymorphisms that predispose to DCIS, we pooled data from 38 studies comprising 5,067 cases of DCIS, 24,584 cases of IDC and 37,467 controls, all genotyped using the iCOGS chip. Results: Most (67 %) of the 76 known breast cancer predisposition loci showed an association with DCIS in the same direction as previously reported for invasive breast cancer. Case-only analysis showed no evidence for differences between associations for IDC and DCIS after considering multiple testing. Analysis by estrogen receptor (ER) status confirmed that loci associated with ER positive IDC were also associated with ER positive DCIS. Analysis of DCIS by grade suggested that two independent SNPs at 11q13.3 near CCND1 were specific to low/intermediate grade DCIS (rs75915166, rs554219). These associations with grade remained after adjusting for ER status and were also found in IDC. We found no novel DCIS-specific loci at a genome wide significance level of P < 5.0x10^-8. Conclusion: In conclusion, this study provides the strongest evidence to date of a shared genetic susceptibility for IDC and DCIS. Studies with larger numbers of DCIS are needed to determine if IDC or DCIS specific loci exist.

Originalsprog	Engelsk
Artikelnummer	22
Tidsskrift	Breast Cancer Research (Online Edition)
Vol/bind	18
Sider (fra-til)	1-15
ISSN	1465-5411
DOI	https://doi.org/10.1186/s13058-016-0675-7
Status	Udgivet - 17 feb. 2016

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10.1186/s13058-016-0675-7Licens: CC BY

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Petridis, C., Brook, M. N., Shah, V., Kohut, K., Gorman, P., Caneppele, M., Levi, D., Papouli, E., Orr, N., Cox, A., Cross, S. S., Dos-Santos-Silva, I., Peto, J., Swerdlow, A., Schoemaker, M. J., Bolla, M. K., Wang, Q., Dennis, J., Michailidou, K., ... Sawyer, E. J. (2016). Genetic predisposition to ductal carcinoma in situ of the breast. Breast Cancer Research (Online Edition), 18, 1-15. Artikel 22. https://doi.org/10.1186/s13058-016-0675-7

Petridis, C, Brook, MN, Shah, V, Kohut, K, Gorman, P, Caneppele, M, Levi, D, Papouli, E, Orr, N, Cox, A, Cross, SS, Dos-Santos-Silva, I, Peto, J, Swerdlow, A, Schoemaker, MJ, Bolla, MK, Wang, Q, Dennis, J, Michailidou, K, Benitez, J, González-Neira, A, Tessier, DC, Vincent, D, Li, J, Figueroa, J, Kristensen, V, Borresen-Dale, A-L, Soucy, P, Simard, J, Milne, RL, Giles, GG, Margolin, S, Lindblom, A, Brüning, T, Brauch, H, Southey, MC, Hopper, JL, Dörk, T, Bogdanova, NV, Kabisch, M, Hamann, U, Schmutzler, RK, Meindl, A, Brenner, H, Arndt, V, Winqvist, R, Pylkäs, K, Fasching, PA, Beckmann, MW, Lubinski, J, Jakubowska, A, Mulligan, AM, Andrulis, IL, Tollenaar, RAEM, Devilee, P, Le Marchand, L, Haiman, CA, Mannermaa, A, Kosma, V-M, Radice, P, Peterlongo, P, Marme, F, Burwinkel, B, van Deurzen, CHM, Hollestelle, A, Miller, N, Kerin, MJ, Lambrechts, D, Floris, G, Wesseling, J, Flyger, H, Bojesen, SE, Yao, S, Ambrosone, CB, Chenevix-Trench, G, Truong, T, Guénel, P, Rudolph, A, Chang-Claude, J, Nevanlinna, H, Blomqvist, C, Czene, K, Brand, JS, Olson, JE, Couch, FJ, Dunning, AM, Hall, P, Easton, DF, Pharoah, PDP, Pinder, SE, Schmidt, MK, Tomlinson, I, Roylance, R, García-Closas, M & Sawyer, EJ 2016, 'Genetic predisposition to ductal carcinoma in situ of the breast', Breast Cancer Research (Online Edition), bind 18, 22, s. 1-15. https://doi.org/10.1186/s13058-016-0675-7

@article{73412419f94e49f7a442dc6ed84bdddf,

title = "Genetic predisposition to ductal carcinoma in situ of the breast",

abstract = "Background: Ductal carcinoma in situ (DCIS) is a non-invasive form of breast cancer. It is often associated with invasive ductal carcinoma (IDC), and is considered to be a non-obligate precursor of IDC. It is not clear to what extent these two forms of cancer share low-risk susceptibility loci, or whether there are differences in the strength of association for shared loci. Methods: To identify genetic polymorphisms that predispose to DCIS, we pooled data from 38 studies comprising 5,067 cases of DCIS, 24,584 cases of IDC and 37,467 controls, all genotyped using the iCOGS chip. Results: Most (67 %) of the 76 known breast cancer predisposition loci showed an association with DCIS in the same direction as previously reported for invasive breast cancer. Case-only analysis showed no evidence for differences between associations for IDC and DCIS after considering multiple testing. Analysis by estrogen receptor (ER) status confirmed that loci associated with ER positive IDC were also associated with ER positive DCIS. Analysis of DCIS by grade suggested that two independent SNPs at 11q13.3 near CCND1 were specific to low/intermediate grade DCIS (rs75915166, rs554219). These associations with grade remained after adjusting for ER status and were also found in IDC. We found no novel DCIS-specific loci at a genome wide significance level of P < 5.0x10-8. Conclusion: In conclusion, this study provides the strongest evidence to date of a shared genetic susceptibility for IDC and DCIS. Studies with larger numbers of DCIS are needed to determine if IDC or DCIS specific loci exist.",

author = "Christos Petridis and Brook, {Mark N} and Vandna Shah and Kelly Kohut and Patricia Gorman and Michele Caneppele and Dina Levi and Efterpi Papouli and Nick Orr and Angela Cox and Cross, {Simon S} and Isabel Dos-Santos-Silva and Julian Peto and Anthony Swerdlow and Schoemaker, {Minouk J} and Bolla, {Manjeet K} and Q. Wang and Joe Dennis and Kyriaki Michailidou and Javier Benitez and Anna Gonz{\'a}lez-Neira and Tessier, {Daniel C} and Daniel Vincent and Jingmei Li and Jonine Figueroa and Vessela Kristensen and Anne-Lise Borresen-Dale and Penny Soucy and Jacques Simard and Milne, {Roger L} and Giles, {Graham G} and Sara Margolin and Annika Lindblom and Thomas Br{\"u}ning and Hiltrud Brauch and Southey, {Melissa C} and Hopper, {John L} and Thilo D{\"o}rk and Bogdanova, {Natalia V} and Maria Kabisch and Ute Hamann and Schmutzler, {Rita K} and Alfons Meindl and Hermann Brenner and Volker Arndt and Robert Winqvist and Katri Pylk{\"a}s and Fasching, {Peter A} and Beckmann, {Matthias W} and Jan Lubinski and Anna Jakubowska and Mulligan, {Anna Marie} and Andrulis, {Irene L} and Tollenaar, {Rob A E M} and Peter Devilee and {Le Marchand}, Loic and Haiman, {Christopher A} and Arto Mannermaa and Veli-Matti Kosma and Paolo Radice and Paolo Peterlongo and Frederik Marme and Barbara Burwinkel and {van Deurzen}, {Carolien H M} and Antoinette Hollestelle and Nicola Miller and Kerin, {Michael J} and Diether Lambrechts and Giuseppe Floris and Jelle Wesseling and Henrik Flyger and Bojesen, {Stig E} and Song Yao and Ambrosone, {Christine B} and Georgia Chenevix-Trench and Th{\'e}r{\`e}se Truong and Pascal Gu{\'e}nel and Anja Rudolph and Jenny Chang-Claude and Heli Nevanlinna and Carl Blomqvist and Kamila Czene and Brand, {Judith S} and Olson, {Janet E} and Couch, {Fergus J} and Dunning, {Alison M} and Per Hall and Easton, {Douglas F} and Pharoah, {Paul D P} and Pinder, {Sarah E} and Schmidt, {Marjanka K} and Ian Tomlinson and Rebecca Roylance and Montserrat Garc{\'i}a-Closas and Sawyer, {Elinor J}",

year = "2016",

month = feb,

day = "17",

doi = "10.1186/s13058-016-0675-7",

language = "English",

volume = "18",

pages = "1--15",

journal = "Breast Cancer Research (Online Edition)",

issn = "1465-5411",

publisher = "BioMed Central Ltd.",

}

TY - JOUR

T1 - Genetic predisposition to ductal carcinoma in situ of the breast

AU - Petridis, Christos

AU - Brook, Mark N

AU - Shah, Vandna

AU - Kohut, Kelly

AU - Gorman, Patricia

AU - Caneppele, Michele

AU - Levi, Dina

AU - Papouli, Efterpi

AU - Orr, Nick

AU - Cox, Angela

AU - Cross, Simon S

AU - Dos-Santos-Silva, Isabel

AU - Peto, Julian

AU - Swerdlow, Anthony

AU - Schoemaker, Minouk J

AU - Bolla, Manjeet K

AU - Wang, Q.

AU - Dennis, Joe

AU - Michailidou, Kyriaki

AU - Benitez, Javier

AU - González-Neira, Anna

AU - Tessier, Daniel C

AU - Vincent, Daniel

AU - Li, Jingmei

AU - Figueroa, Jonine

AU - Kristensen, Vessela

AU - Borresen-Dale, Anne-Lise

AU - Soucy, Penny

AU - Simard, Jacques

AU - Milne, Roger L

AU - Giles, Graham G

AU - Margolin, Sara

AU - Lindblom, Annika

AU - Brüning, Thomas

AU - Brauch, Hiltrud

AU - Southey, Melissa C

AU - Hopper, John L

AU - Dörk, Thilo

AU - Bogdanova, Natalia V

AU - Kabisch, Maria

AU - Hamann, Ute

AU - Schmutzler, Rita K

AU - Meindl, Alfons

AU - Brenner, Hermann

AU - Arndt, Volker

AU - Winqvist, Robert

AU - Pylkäs, Katri

AU - Fasching, Peter A

AU - Beckmann, Matthias W

AU - Lubinski, Jan

AU - Jakubowska, Anna

AU - Mulligan, Anna Marie

AU - Andrulis, Irene L

AU - Tollenaar, Rob A E M

AU - Devilee, Peter

AU - Le Marchand, Loic

AU - Haiman, Christopher A

AU - Mannermaa, Arto

AU - Kosma, Veli-Matti

AU - Radice, Paolo

AU - Peterlongo, Paolo

AU - Marme, Frederik

AU - Burwinkel, Barbara

AU - van Deurzen, Carolien H M

AU - Hollestelle, Antoinette

AU - Miller, Nicola

AU - Kerin, Michael J

AU - Lambrechts, Diether

AU - Floris, Giuseppe

AU - Wesseling, Jelle

AU - Flyger, Henrik

AU - Bojesen, Stig E

AU - Yao, Song

AU - Ambrosone, Christine B

AU - Chenevix-Trench, Georgia

AU - Truong, Thérèse

AU - Guénel, Pascal

AU - Rudolph, Anja

AU - Chang-Claude, Jenny

AU - Nevanlinna, Heli

AU - Blomqvist, Carl

AU - Czene, Kamila

AU - Brand, Judith S

AU - Olson, Janet E

AU - Couch, Fergus J

AU - Dunning, Alison M

AU - Hall, Per

AU - Easton, Douglas F

AU - Pharoah, Paul D P

AU - Pinder, Sarah E

AU - Schmidt, Marjanka K

AU - Tomlinson, Ian

AU - Roylance, Rebecca

AU - García-Closas, Montserrat

AU - Sawyer, Elinor J

PY - 2016/2/17

Y1 - 2016/2/17

N2 - Background: Ductal carcinoma in situ (DCIS) is a non-invasive form of breast cancer. It is often associated with invasive ductal carcinoma (IDC), and is considered to be a non-obligate precursor of IDC. It is not clear to what extent these two forms of cancer share low-risk susceptibility loci, or whether there are differences in the strength of association for shared loci. Methods: To identify genetic polymorphisms that predispose to DCIS, we pooled data from 38 studies comprising 5,067 cases of DCIS, 24,584 cases of IDC and 37,467 controls, all genotyped using the iCOGS chip. Results: Most (67 %) of the 76 known breast cancer predisposition loci showed an association with DCIS in the same direction as previously reported for invasive breast cancer. Case-only analysis showed no evidence for differences between associations for IDC and DCIS after considering multiple testing. Analysis by estrogen receptor (ER) status confirmed that loci associated with ER positive IDC were also associated with ER positive DCIS. Analysis of DCIS by grade suggested that two independent SNPs at 11q13.3 near CCND1 were specific to low/intermediate grade DCIS (rs75915166, rs554219). These associations with grade remained after adjusting for ER status and were also found in IDC. We found no novel DCIS-specific loci at a genome wide significance level of P < 5.0x10-8. Conclusion: In conclusion, this study provides the strongest evidence to date of a shared genetic susceptibility for IDC and DCIS. Studies with larger numbers of DCIS are needed to determine if IDC or DCIS specific loci exist.

AB - Background: Ductal carcinoma in situ (DCIS) is a non-invasive form of breast cancer. It is often associated with invasive ductal carcinoma (IDC), and is considered to be a non-obligate precursor of IDC. It is not clear to what extent these two forms of cancer share low-risk susceptibility loci, or whether there are differences in the strength of association for shared loci. Methods: To identify genetic polymorphisms that predispose to DCIS, we pooled data from 38 studies comprising 5,067 cases of DCIS, 24,584 cases of IDC and 37,467 controls, all genotyped using the iCOGS chip. Results: Most (67 %) of the 76 known breast cancer predisposition loci showed an association with DCIS in the same direction as previously reported for invasive breast cancer. Case-only analysis showed no evidence for differences between associations for IDC and DCIS after considering multiple testing. Analysis by estrogen receptor (ER) status confirmed that loci associated with ER positive IDC were also associated with ER positive DCIS. Analysis of DCIS by grade suggested that two independent SNPs at 11q13.3 near CCND1 were specific to low/intermediate grade DCIS (rs75915166, rs554219). These associations with grade remained after adjusting for ER status and were also found in IDC. We found no novel DCIS-specific loci at a genome wide significance level of P < 5.0x10-8. Conclusion: In conclusion, this study provides the strongest evidence to date of a shared genetic susceptibility for IDC and DCIS. Studies with larger numbers of DCIS are needed to determine if IDC or DCIS specific loci exist.

U2 - 10.1186/s13058-016-0675-7

DO - 10.1186/s13058-016-0675-7

M3 - Journal article

C2 - 26884359

SN - 1465-5411

VL - 18

SP - 1

EP - 15

JO - Breast Cancer Research (Online Edition)

JF - Breast Cancer Research (Online Edition)

M1 - 22

ER -

Genetic predisposition to ductal carcinoma in situ of the breast

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