How Many Etiological Subtypes of Breast Cancer: Two, Three, Four, Or More?

被引:181
作者
Anderson, William F. [1 ]
Rosenberg, Philip S. [1 ]
Prat, Aleix [3 ]
Perou, Charles M. [4 ]
Sherman, Mark E. [2 ]
机构
[1] NCI, Div Canc Epidemiol & Genet, Biostat Branch, NIH, Bethesda, MD 20892 USA
[2] NCI, Canc Prevent Div, NIH, Bethesda, MD 20892 USA
[3] Vall dHebron Inst Oncol, Translat Genom Grp, Barcelona, Spain
[4] Univ N Carolina, Lineberger Comprehens Canc Ctr, Dept Genet & Pathol & Lab Med, Chapel Hill, NC 27599 USA
来源
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE | 2014年 / 106卷 / 08期
基金
美国国家卫生研究院;
关键词
BASAL-LIKE SUBTYPE; DIFFERENT HISTOPATHOLOGIC TYPES; BIMODAL AGE DISTRIBUTION; ESTROGEN-RECEPTOR STATUS; GENOME-WIDE ASSOCIATION; PERIOD-COHORT ANALYSIS; HORMONAL RISK-FACTORS; SHORT-TERM INCREASE; CARCINOMA IN-SITU; STEM-CELLS;
D O I
10.1093/jnci/dju165
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Breast cancer is a heterogeneous disease, divisible into a variable number of clinical subtypes. A fundamental question is how many etiological classes underlie the clinical spectrum of breast cancer? An etiological subtype reflects a grouping with a common set of causes, whereas a clinical subtype represents a grouping with similar prognosis and/or prediction. Herein, we review the evidence for breast cancer etiological heterogeneity. We then evaluate the etiological evidence with mRNA profiling data. A bimodal age distribution at diagnosis with peak frequencies near ages 50 and 70 years is a fundamental characteristic of breast cancer for important tumor features, clinical characteristics, risk factor profiles, and molecular subtypes. The bimodal peak frequencies at diagnosis divide breast cancer overall into a "mixture" of two main components in varying proportions in different cancer populations. The first breast cancer tends to arise early in life with modal age-at-diagnosis near 50 years and generally behaves aggressively. The second breast cancer occurs later in life with modal age near 70 years and usually portends a more indolent clinical course. These epidemiological and molecular data are consistent with a two-component mixture model and compatible with a hierarchal view of breast cancers arising from two main cell types of origin. Notwithstanding the potential added value of more detailed categorizations for personalized breast cancer treatment, we suggest that the development of better criteria to identify the two proposed etiologic classes would advance breast cancer research and prevention.
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页数:11
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