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Circulating tumor cells expressing cancer stem cell marker CD44 as a diagnostic biomarker in patients with gastric cancer

Epithelial cell adhesion molecule (EpCAM) is a marker for circulating tumor cells (CTCs) in various types of cancer, while cluster of differentiation 44 (CD44) is a marker for gastric cancer (GC) stem cells. To evaluate the clinical significance of CD44(+) CTCs in patients with GC in the present stu...

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Detalles Bibliográficos
Autores principales: Watanabe, Toru, Okumura, Tomoyuki, Hirano, Katsuhisa, Yamaguchi, Tetsuji, Sekine, Shinichi, Nagata, Takuya, Tsukada, Kazuhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5244869/
https://www.ncbi.nlm.nih.gov/pubmed/28123556
http://dx.doi.org/10.3892/ol.2016.5432
Descripción
Sumario:Epithelial cell adhesion molecule (EpCAM) is a marker for circulating tumor cells (CTCs) in various types of cancer, while cluster of differentiation 44 (CD44) is a marker for gastric cancer (GC) stem cells. To evaluate the clinical significance of CD44(+) CTCs in patients with GC in the present study, the number of EpCAM(+)CD44(+) and EpCAM(+)CD44(−) cells were detected in the peripheral blood of 26 GC patients and 12 healthy volunteers using flow cytometry. The number (mean ± standard deviation) of EpCAM(+)CD44(+) cells in the GC patients and healthy volunteers was 69.9±52.0 and 0.91±2.10, respectively (P=0.0001), while that of EpCAM(+)CD44(−) cells was 59.1±88.0 and 9.83±9.91, respectively (P=0.0313). The sensitivity and specificity of EpCAM(+)CD44(+) cell detection for the identification of GC patients were 92.3 and 100%, respectively. By contrast, the values of EpCAM(+)CD44(−) cell detection were 76.9 and 83.3%, respectively. The number of EpCAM(+)CD44(+) cells in the GC patients was correlated with the disease stage (P=0.0423), the depth of the tumor (P=0.0314) and venous invasion (P=0.0184) in the resected tumor specimens, while the number of EpCAM(+)CD44(−) cells did not correlate with any clinicopathological factors. The number of EpCAM(+)CD44(+) cells significantly decreased following surgical resection of the tumor or induction of systemic chemotherapy. Additionally, atypical cells with a high nuclear to cytoplasmic ratio were morphologically detected in the sorted EpCAM(+)CD44(+) cells. These results suggested that CD44(+) CTCs, but not CD44(−) CTCs, reflect the malignant status of the primary tumor in patients with GC, providing a candidate biomarker for diagnosis and treatment response.