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Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with prognosis of estrogen receptor-negative breast cancer after chemotherapy

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dc.contributor.authorLei, Jieping-
dc.contributor.authorRudolph, Anja-
dc.contributor.authorMoysich, Kirsten B-
dc.contributor.authorRafiq, Sajjad-
dc.contributor.authorBehrens, Sabine-
dc.contributor.authorGoode, Ellen L-
dc.contributor.authorPharoah, Paul P-
dc.contributor.authorSeibold, Petra-
dc.contributor.authorFasching, Peter A-
dc.contributor.authorAndrulis, Irene L-
dc.contributor.authorKristensen, Vessela N-
dc.contributor.authorCouch, Fergus J-
dc.contributor.authorHamann, Ute-
dc.contributor.authorHooning, Maartje J-
dc.contributor.authorNevanlinna, Heli-
dc.contributor.authorEilber, Ursula-
dc.contributor.authorBolla, Manjeet K-
dc.contributor.authorDennis, Joe-
dc.contributor.authorWang, Qin-
dc.contributor.authorLindblom, Annika-
dc.contributor.authorMannermaa, Arto-
dc.contributor.authorLambrechts, Diether-
dc.contributor.authorGarcía-Closas, Montserrat-
dc.contributor.authorHall, Per-
dc.contributor.authorChenevix-Trench, Georgia-
dc.contributor.authorShah, Mitul-
dc.contributor.authorLuben, Robert-
dc.contributor.authorHaeberle, Lothar-
dc.contributor.authorEkici, Arif B-
dc.contributor.authorBeckmann, Matthias W-
dc.contributor.authorKnight, Julia A-
dc.contributor.authorGlendon, Gord-
dc.contributor.authorTchatchou, Sandrine-
dc.contributor.authorAlnæs, Grethe I G-
dc.contributor.authorBorresen-Dale, Anne-Lise-
dc.contributor.authorNord, Silje-
dc.contributor.authorOlson, Janet E-
dc.contributor.authorHallberg, Emily-
dc.contributor.authorVachon, Celine-
dc.contributor.authorTorres, Diana-
dc.contributor.authorUlmer, Hans-Ulrich-
dc.contributor.authorRüdiger, Thomas-
dc.contributor.authorJager, Agnes-
dc.contributor.authorvan Deurzen, Carolien H-
dc.contributor.authorTilanus-Linthorst, Madeleine M-
dc.contributor.authorMuranen, Taru A-
dc.contributor.authorAittomäki, Kristiina-
dc.contributor.authorBlomqvist, Carl-
dc.contributor.authorMargolin, Sara-
dc.contributor.authorKosma, Veli-Matti-
dc.contributor.authorHartikainen, Jaana M-
dc.contributor.authorKataja, Vesa-
dc.contributor.authorHatse, Sigrid-
dc.contributor.authorWildiers, Hans-
dc.contributor.authorSmeets, Ann-
dc.contributor.authorFigueroa, Jonine-
dc.contributor.authorChanock, Stephen J-
dc.contributor.authorLissowska, Jolanta-
dc.contributor.authorLi, Jingmei-
dc.contributor.authorHumphreys, Keith-
dc.contributor.authorPhillips, Kelly-Anne-
dc.contributor.authorLinn, Sabine-
dc.contributor.authorCornelissen, Sten-
dc.contributor.authorvan den Broek, Sandra A J-
dc.contributor.authorKang, Daehee-
dc.contributor.authorChoi, Ji-Yeob-
dc.contributor.authorPark, Sue K-
dc.contributor.authorYoo, Keun-Young-
dc.contributor.authorHsiung, Chia-Ni-
dc.contributor.authorWu, Pei-Ei-
dc.contributor.authorHou, Ming-Feng-
dc.contributor.authorShen, Chen-Yang-
dc.contributor.authorTeo, Soo H-
dc.contributor.authorTaib, Nur A M-
dc.contributor.authorYip, Cheng H-
dc.contributor.authorHo, Gwo F-
dc.contributor.authorMatsuo, Keitaro-
dc.contributor.authorIto, Hidemi-
dc.contributor.authorIwata, Hiroji-
dc.contributor.authorTajima, Kazuo-
dc.contributor.authorDunning, Alison M-
dc.contributor.authorBenitez, Javier-
dc.contributor.authorCzene, Kamila-
dc.contributor.authorSucheston, Lara E-
dc.contributor.authorMaishman, Tom-
dc.contributor.authorTapper, William J-
dc.contributor.authorEccles, Diana-
dc.contributor.authorEaston, Douglas F-
dc.contributor.authorSchmidt, Marjanka K-
dc.contributor.authorChang-Claude, Jenny-
dc.date.accessioned2017-02-06T00:27:55Z-
dc.date.available2017-02-06T00:27:55Z-
dc.date.issued2015-02-10-
dc.identifier.citationBreast Cancer Research, 17(1):18ko_KR
dc.identifier.urihttps://hdl.handle.net/10371/100414-
dc.descriptionThis is an Open Access article distributed under the terms of the Creative Commons
Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
ko_KR
dc.description.abstractAbstract

Introduction
Tumor lymphocyte infiltration is associated with clinical response to chemotherapy in estrogen receptor (ER) negative breast cancer. To identify variants in immunosuppressive pathway genes associated with prognosis after adjuvant chemotherapy for ER-negative patients, we studied stage I-III invasive breast cancer patients of European ancestry, including 9,334 ER-positive (3,151 treated with chemotherapy) and 2,334 ER-negative patients (1,499 treated with chemotherapy).


Methods
We pooled data from sixteen studies from the Breast Cancer Association Consortium (BCAC), and employed two independent studies for replications. Overall 3,610 single nucleotide polymorphisms (SNPs) in 133 genes were genotyped as part of the Collaborative Oncological Gene-environment Study, in which phenotype and clinical data were collected and harmonized. Multivariable Cox proportional hazard regression was used to assess genetic associations with overall survival (OS) and breast cancer-specific survival (BCSS). Heterogeneity according to chemotherapy or ER status was evaluated with the log-likelihood ratio test.


Results
Three independent SNPs in TGFBR2 and IL12B were associated with OS (P <10−3) solely in ER-negative patients after chemotherapy (267 events). Poorer OS associated with TGFBR2 rs1367610 (G > C) (per allele hazard ratio (HR) 1.54 (95% confidence interval (CI) 1.22 to 1.95), P = 3.08 × 10−4) was not found in ER-negative patients without chemotherapy or ER-positive patients with chemotherapy (P for interaction <10−3). Two SNPs in IL12B (r2 = 0.20) showed different associations with ER-negative disease after chemotherapy: rs2546892 (G > A) with poorer OS (HR 1.50 (95% CI 1.21 to 1.86), P = 1.81 × 10−4), and rs2853694 (A > C) with improved OS (HR 0.73 (95% CI 0.61 to 0.87), P = 3.67 × 10−4). Similar associations were observed with BCSS. Association with TGFBR2 rs1367610 but not IL12B variants replicated using BCAC Asian samples and the independent Prospective Study of Outcomes in Sporadic versus Hereditary Breast Cancer Study and yielded a combined HR of 1.57 ((95% CI 1.28 to 1.94), P = 2.05 × 10−5) without study heterogeneity.


Conclusions

TGFBR2 variants may have prognostic and predictive value in ER-negative breast cancer patients treated with adjuvant chemotherapy. Our findings provide further insights into the development of immunotherapeutic targets for ER-negative breast cancer.
ko_KR
dc.language.isoenko_KR
dc.publisherBioMed Centralko_KR
dc.titleAssessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with prognosis of estrogen receptor-negative breast cancer after chemotherapyko_KR
dc.typeArticleko_KR
dc.contributor.AlternativeAuthor강대희-
dc.contributor.AlternativeAuthor최지엽-
dc.contributor.AlternativeAuthor유근영-
dc.identifier.doi10.1186/s13058-015-0522-2-
dc.language.rfc3066en-
dc.rights.holderLei et al.; licensee BioMed Central.-
dc.date.updated2017-02-05T03:04:28Z-
Appears in Collections:
College of Medicine/School of Medicine (의과대학/대학원)Preventive Medicine (예방의학전공)Journal Papers (저널논문_예방의학전공)
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