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Surgical Pathology
304
Id: SA61
High-Level Expression of Standard Form CD44 in Distant Metastasis of Estrogen Receptor-Negative Breast
Cancer
Wei Zheng, Lichao Zhao, Shin-Ae Kang, Takemi Tanaka, University of Oklahoma Health Science Center
Breast cancer is the most common malignancy in women in the United States, and hematogenous metastasis
accounts for the majority of cancer-related morbidity and mortality, yet the mechanism remains unclear. CD44 (a
cell surface receptor) has been implicated to regulate the adhesion of circulating cancer cells to the endothelium by
interaction with vascular adhesion molecules selectins. However, to date, no comparison of CD44s expression and
breast cancer subtype in distant metastases of human patient has been reported. This study, for the first time, to our
knowledge, reveals that high-level expression of standard form CD44 (CD44s) is uniquely associated with estrogen
receptor (ER)-negative breast cancers but not other subtypes of breast cancer in distant metastases, indicating CD44s
as a potential marker in predicting breast cancer aggressiveness. CD44s and E-selectin expression levels were
analyzed by immunohistochemistry using 31 brain and pulmonary metastases of breast cancer from female patients.
Semiquantitative scoring of CD44s and E-selectin expression was performed blindly. Association/correlation of
CD44s and ER or progesterone receptor (PR) status was analyzed using Mann-Whitney test. Results indicate highlevel expression of CD44s in ER-negative brain and pulmonary metastases of breast cancer in comparison to ER+
metastases. The expression of CD44s was inversely correlated with ER statuses. However, no correlation was found
between CD44s and PR status. E-selectin expression was also highly upregulated in metastatic carcinomas. These
findings suggest a distinct role for CD44s in ER-negative breast cancers, and propose CD44 as a potential marker in
predicting a metastatic phenotype of ER-negative breast cancer.
© American Society for Clinical Pathology
Am J Clin Pathol 2015;144:A304