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Elucidating prognosis and biology of breast cancer arising in young women using gene expression profiling
- Source :
- Clinical cancer research : an official journal of the American Association for Cancer Research. 18(5)
- Publication Year :
- 2012
-
Abstract
- Purpose: Breast cancer in young women is associated with poor prognosis. We aimed to define the role of gene expression signatures in predicting prognosis in young women and to understand biological differences according to age. Experimental Design: Patients were assigned to molecular subtypes [estrogen receptor (ER)+/HER2−; HER2+, ER−/HER2−)] using a three-gene classifier. We evaluated whether previously published proliferation, stroma, and immune-related gene signatures added prognostic information to Adjuvant! online and tested their interaction with age in a Cox model for relapse-free survival (RFS). Furthermore, we evaluated the association between candidate age-related genes or gene sets with age in an adjusted linear regression model. Results: A total of 3,522 patients (20 data sets) were eligible. Patients aged 40 years or less had a higher proportion of ER−/HER2− tumors (P < 0.0001) and were associated with poorer RFS after adjustment for breast cancer subtype, tumor size, nodal status, and histologic grade and stratification for data set and treatment modality (HR = 1.34, 95% CI = 1.10–1.63, P = 0.004). The proliferation gene signatures showed no significant interaction with age in ER+/HER2− tumors after adjustment for Adjuvant! online. Further analyses suggested that breast cancer in the young is enriched with processes related to immature mammary epithelial cells (luminal progenitors, mammary stem, c-kit, RANKL) and growth factor signaling in two independent cohorts (n = 1,188 and 2,334). Conclusions: Proliferation-related prognostic gene signatures can aid treatment decision-making for young women. However, breast cancer arising at a young age seems to be biologically distinct beyond subtype distribution. Separate therapeutic approaches such as targeting RANKL or mammary stem cells could therefore be needed. Clin Cancer Res; 18(5); 1341–51. ©2012 AACR.
- Subjects :
- Oncology
Adult
Cancer Research
medicine.medical_specialty
Receptor, ErbB-2
Population
Estrogen receptor
Breast Neoplasms
Bioinformatics
Metastasis
Cohort Studies
Young Adult
Breast cancer
Internal medicine
medicine
Humans
Young adult
education
Survival analysis
Aged
education.field_of_study
biology
business.industry
Gene Expression Profiling
Age Factors
Middle Aged
medicine.disease
Prognosis
Survival Analysis
Gene expression profiling
Receptors, Estrogen
RANKL
biology.protein
Female
business
Subjects
Details
- ISSN :
- 15573265
- Volume :
- 18
- Issue :
- 5
- Database :
- OpenAIRE
- Journal :
- Clinical cancer research : an official journal of the American Association for Cancer Research
- Accession number :
- edsair.doi.dedup.....7ab700b7fd778bc8e90bbb02e3a665f4