Genetic predisposition to ductal carcinoma in situ of the breast. Issue 1 (December 2016)
- Record Type:
- Journal Article
- Title:
- Genetic predisposition to ductal carcinoma in situ of the breast. Issue 1 (December 2016)
- Main Title:
- Genetic predisposition to ductal carcinoma in situ of the breast
- Authors:
- Petridis, Christos
Brook, Mark
Shah, Vandna
Kohut, Kelly
Gorman, Patricia
Caneppele, Michele
Levi, Dina
Papouli, Efterpi
Orr, Nick
Cox, Angela
Cross, Simon
dos-Santos-Silva, Isabel
Peto, Julian
Swerdlow, Anthony
Schoemaker, Minouk
Bolla, Manjeet
Wang, Qin
Dennis, Joe
Michailidou, Kyriaki
Benitez, Javier
González-Neira, Anna
Tessier, Daniel
Vincent, Daniel
Li, Jingmei
Figueroa, Jonine
Kristensen, Vessela
Borresen-Dale, Anne-Lise
Soucy, Penny
Simard, Jacques
Milne, Roger
Giles, Graham
Margolin, Sara
Lindblom, Annika
Brüning, Thomas
Brauch, Hiltrud
Southey, Melissa
Hopper, John
Dörk, Thilo
Bogdanova, Natalia
Kabisch, Maria
Hamann, Ute
Schmutzler, Rita
Meindl, Alfons
Brenner, Hermann
Arndt, Volker
Winqvist, Robert
Pylkäs, Katri
Fasching, Peter
Beckmann, Matthias
Lubinski, Jan
Jakubowska, Anna
Mulligan, Anna
Andrulis, Irene
Tollenaar, Rob
Devilee, Peter
Le Marchand, Loic
Haiman, Christopher
Mannermaa, Arto
Kosma, Veli-Matti
Radice, Paolo
Peterlongo, Paolo
Marme, Frederik
Burwinkel, Barbara
van Deurzen, Carolien
Hollestelle, Antoinette
Miller, Nicola
Kerin, Michael
Lambrechts, Diether
Floris, Giuseppe
Wesseling, Jelle
Flyger, Henrik
Bojesen, Stig
Yao, Song
Ambrosone, Christine
Chenevix-Trench, Georgia
Truong, Thérèse
Guénel, Pascal
Rudolph, Anja
Chang-Claude, Jenny
Nevanlinna, Heli
Blomqvist, Carl
Czene, Kamila
Brand, Judith
Olson, Janet
Couch, Fergus
Dunning, Alison
Hall, Per
Easton, Douglas
Pharoah, Paul
Pinder, Sarah
Schmidt, Marjanka
Tomlinson, Ian
Roylance, Rebecca
García-Closas, Montserrat
Sawyer, Elinor
… (more) - Abstract:
- Abstract Background Ductal carcinomain 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 nearCCND1 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 ofP < 5.0x10-8 . Conclusion In conclusion, this study provides the strongest evidence to date of a shared genetic susceptibility for IDC andAbstract Background Ductal carcinomain 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 nearCCND1 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 ofP < 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. … (more)
- Is Part Of:
- Breast cancer research. Volume 18:Issue 1(2016)
- Journal:
- Breast cancer research
- Issue:
- Volume 18:Issue 1(2016)
- Issue Display:
- Volume 18, Issue 1 (2016)
- Year:
- 2016
- Volume:
- 18
- Issue:
- 1
- Issue Sort Value:
- 2016-0018-0001-0000
- Page Start:
- 1
- Page End:
- 15
- Publication Date:
- 2016-12
- Subjects:
- Ductal carcinoma in situ -- Association study -- Genetic predisposition -- Common variants
Breast -- Cancer -- Periodicals
616.99449 - Journal URLs:
- https://breast-cancer-research.biomedcentral.com/ ↗
http://www.bibliothek.uni-regensburg.de/ezeit/?2041618 ↗
http://link.springer.com/ ↗
http://pubmedcentral.nih.gov/tocrender.fcgi?journal=6 ↗
http://www.biomedcentral.com/1465-5411/ ↗ - DOI:
- 10.1186/s13058-016-0675-7 ↗
- Languages:
- English
- ISSNs:
- 1465-542X
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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- British Library DSC - BLDSS-3PM
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