Please use this identifier to cite or link to this item:
Title: Association between breast cancer risk and disease aggressiveness: Characterizing underlying gene expression patterns
Authors: Ugalde-Morales, Emilio
Grassmann, Felix
Humphreys, Keith
Li, Jingmei 
Eriksson, Mikael
Tobin, Nicholas P.
Borg, Å.
Vallon-Christersson, Johan
Hall, Per
Czene, Kamila
Keywords: breast cancer
gene expression
Tyrer-Cuzick risk score
Issue Date: 5-Sep-2020
Publisher: Wiley-Liss Inc.
Citation: Ugalde-Morales, Emilio, Grassmann, Felix, Humphreys, Keith, Li, Jingmei, Eriksson, Mikael, Tobin, Nicholas P., Borg, Å., Vallon-Christersson, Johan, Hall, Per, Czene, Kamila (2020-09-05). Association between breast cancer risk and disease aggressiveness: Characterizing underlying gene expression patterns. International Journal of Cancer 148 (4) : 884-894. ScholarBank@NUS Repository.
Rights: Attribution 4.0 International
Abstract: The association between breast cancer risk defined by the Tyrer-Cuzick score (TC) and disease prognosis is not well established. Here, we investigated the relationship between 5-year TC and disease aggressiveness and then characterized underlying molecular processes. In a case-only study (n = 2474), we studied the association of TC with molecular subtypes and tumor characteristics. In a subset of patients (n = 672), we correlated gene expression to TC and computed a low-risk TC gene expression (TC-Gx) profile, that is, a profile expected to be negatively associated with risk, which we used to test for association with disease aggressiveness. We performed enrichment analysis to pinpoint molecular processes likely to be altered in low-risk tumors. A higher TC was found to be inversely associated with more aggressive surrogate molecular subtypes and tumor characteristics (P <.05) including Ki-67 proliferation status (P < 5 × 10?07). Our low-risk TC-Gx, based on the weighted sum of 37 expression values of genes strongly correlated with TC, was associated with basal-like (P < 5 × 10?13), HER2-enriched subtype (P < 5 × 10?07) and worse 10-year breast cancer-specific survival (log-rank P < 5 × 10?04). Associations between low-risk TC-Gx and more aggressive molecular subtypes were replicated in an independent cohort from The Cancer Genome Atlas database (n = 975). Gene expression that correlated with low TC was enriched in proliferation and oncogenic signaling pathways (FDR < 0.05). Moreover, higher proliferation was a key factor explaining the association with worse survival. Women who developed breast cancer despite having a low risk were diagnosed with more aggressive tumors and had a worse prognosis, most likely driven by increased proliferation. Our findings imply the need to establish risk factors associated with more aggressive breast cancer subtypes. © 2020 The Authors. International Journal of Cancer published by John Wiley & Sons Ltd on behalf of Union for International Cancer Control.
Source Title: International Journal of Cancer
ISSN: 0020-7136
DOI: 10.1002/ijc.33270
Rights: Attribution 4.0 International
Appears in Collections:Staff Publications

Show full item record
Files in This Item:
File Description SizeFormatAccess SettingsVersion 
10_1002_ijc_33270.pdf853.53 kBAdobe PDF



Google ScholarTM



This item is licensed under a Creative Commons License Creative Commons