Mechanisms of Disease: breast tumor pathogenesis and the role of the myoepithelial cell

The myoepithelial cell exerts profound effects on breast tumor cell behavior and resides close to abnormally proliferating breast epithelial cells in precancerous ductal carcinoma in situ (DCIS) tumors. These cells also form a natural border separating breast epithelial cells from stromal angiogenes...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Nature clinical practice. Oncology 2006-03, Vol.3 (3), p.138-151
Hauptverfasser: Barsky, Sanford H, Karlin, Nina J
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:The myoepithelial cell exerts profound effects on breast tumor cell behavior and resides close to abnormally proliferating breast epithelial cells in precancerous ductal carcinoma in situ (DCIS) tumors. These cells also form a natural border separating breast epithelial cells from stromal angiogenesis. Barsky and Karlin discuss the role myoepithelial cells may have in inhibiting the progression of DCIS to invasive breast cancer, and the functional studies that are elucidating the anti-invasive and anti-angiogenic phenotypes of these cells. Breast cancer and precancer cells are influenced by important paracrine regulation from the breast microenvironment, which might be as great a determinant of breast cancer behavior as the specific oncogenic or tumor-suppressive alterations occurring within malignant breast cells. Myoepithelial cells exert profound effects on breast tumor cell behavior, and lie in juxtaposition to abnormally proliferating breast epithelial cells in precancerous disease states such as ductal carcinoma in situ (DCIS). Myoepithelial cells also form a natural border separating breast epithelial cells from stromal angiogenesis. These anatomical relationships suggest that myoepithelial cells might inhibit both the progression of DCIS to invasive breast cancer, and carcinoma-induced angiogenesis. Our ability to study myoepithelial cells has been fostered by recent technical advances in cell selection and sorting procedures, improved selective media, and high throughput technologies, which are able to assess the gene and protein expression profiles within cells. In addition, the establishment of a number of immortalized cell lines and xenografts of myoepithelial cells derived from benign human myoepithelial tumors of diverse sources has provided a self-renewing cell source through which to study the phenotype of myoepithelial cells. Studies of primary and immortalized myoepithelial cell lines indicate that these cells exhibit a natural tumor suppressor function. Functional studies show that these cells have anti-invasive and antiangiogenic phenotypes. Key Points Myoepithelial cells surround both normal ducts and precancerous lesions of the breast, and form a natural border separating epithelial cells from stromal cells By forming this natural border, myoepithelial cells are thought to negatively regulate tumor invasion, angiogenesis and metastasis Tumors of the myoepithelium are uncommon and usually benign, although highly aggressive malignant my
ISSN:1743-4254
1759-4774
1743-4262
1759-4782
DOI:10.1038/ncponc0450