4.6 Review

Impact of aging on the biology of breast cancer

Journal

CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY
Volume 66, Issue 1, Pages 65-74

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.critrevonc.2007.09.001

Keywords

age-associated malignancies; breast cancer; mammary gland involution; cellular senescence; prognostic and predictive biomarkers; estrogen receptor

Funding

  1. NATIONAL CANCER INSTITUTE [R01CA071468, P50CA058207] Funding Source: NIH RePORTER
  2. NATIONAL INSTITUTE ON AGING [R01AG020521, P01AG025901] Funding Source: NIH RePORTER
  3. NCI NIH HHS [R01-CA71468, P50 CA058207, P50 CA058207-140014, P50-CA58207, R01 CA071468, R01 CA071468-14] Funding Source: Medline
  4. NIA NIH HHS [R01-AG020521, R01 AG020521-05, P01 AG025901, P01 AG025901-02, P01-AG025901, R01 AG020521] Funding Source: Medline

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Breast cancer is a heterogeneous malignancy; its age-specific incidence profile rises exponentially until menopause and increases more slowly thereafter, reflecting the superimposition of early-onset and late-onset breast cancer rates. While early-onset breast cancers largely represent inherited or early life transforming effects on immature mammary epithelium, late-onset breast cancers likely follow extended exposures to promoting stimuli of susceptible epithelium that has failed to age normally. Among stimuli thought to promote late-onset breast tumorigenesis are the altered extracellular matrix and secreted products of senescent fibroblasts; however, the extent to which these senescent influences exist within the aging breast remains unknown. Clinical observations and biomarker studies indicate that late-onset breast cancers grow more slowly and are biologically less aggressive than early-onset breast cancers, even when controlled for hormone receptor (e.g. estrogen receptor, ER) and growth factor receptor (e.g. HER2) expression, supporting the conclusion that the biology of breast cancer is age-dependent. (C) 2007 Elsevier Ireland Ltd. All rights reserved.

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