Recently, it was observed that
nestin is preferentially expressed in basal/myoepithelial cells of the mammary gland, and that this intermediate filament may be used as a myoepithelial marker. However, the clinical and prognostic implications of
nestin as a marker for
breast cancer are still unclear. We examined
mastectomy specimens from 150 breast
cancers and matching, adjacent non-cancerous tissues using immunohistochemistry and western blotting. Overall,
triple-negative breast cancers - that is, breast
cancers that do not express
estrogen receptors (ER),
progesterone receptors (PR), or
human epidermal growth factor receptor 2 (HER2/neu) - had higher expression rates for
nestin than the other breast
cancers (57.14%vs 9.30%; P < 0.001). In
triple-negative breast cancers, significantly increased
nestin expression rates were observed in patients with
lymph node metastasis compared with those without node
metastasis (25.00%vs 76.92%; P = 0.032). A similar phenomenon was observed for invasive
ductal carcinomas compared with
ductal carcinoma in situ (16.67%vs 73.33%; P = 0.046).
Nestin expression was also found to be significantly related to ER, PR, and P53 expression (P < 0.05).
Nestin expression was associated with both shorter
breast cancer-specific survival and poor relapse-free survival in the lymph node-positive group (P = 0.028 and P = 0.012 respectively). After Cox regression was carried out,
nestin was not shown to be an independent prognostic factor for
breast cancer. These findings substantiate the possibility of using
nestin as a marker for
triple-negative breast cancer.
Triple-negative breast cancer progression is associated with
nestin; however, the underlying mechanisms of this relationship require further investigation.