Department of Oncology, Vejle Hospital, Kabbeltoft 25, 7100 Vejle, Denmark.
J Oncol. 2011;2011:620523. doi: 10.1155/2011/620523. Epub 2011 Aug 29.
Epithelial ovarian cancer stem cells (EOC stem cells) have been associated with recurrence and chemoresistance. CD44 and CK18 are highly expressed in cancer stem cells and function as tools for their identification and characterization. We investigated the association between the number of CD44+ EOC stem cells in ovarian cancer tumors and progression-free survival. EOC stem cells exist as clusters located close to the stroma forming the cancer stem cell "niche". 17.1% of the samples reveled high number of CD44+ EOC stem cells (>20% positive cells). In addition, the number of CD44+ EOC stem cells was significantly higher in patients with early-stage ovarian cancer (FIGO I/II), and it was associated with shorter progression-free survival (P = 0.026). This study suggests that quantification of the number of EOC stem cells in the tumor can be used as a predictor of disease and could be applied for treatment selection in early-stage ovarian cancer.
上皮性卵巢癌干细胞(EOC 干细胞)与复发和化疗耐药有关。CD44 和 CK18 在癌症干细胞中高表达,并作为其鉴定和特征描述的工具。我们研究了卵巢癌肿瘤中 CD44+EOC 干细胞数量与无进展生存期之间的关系。EOC 干细胞作为位于靠近形成癌症干细胞“生态位”的基质的簇存在。17.1%的样本显示出高数量的 CD44+EOC 干细胞(>20%的阳性细胞)。此外,早期卵巢癌(FIGO I/II)患者的 CD44+EOC 干细胞数量明显更高,且与无进展生存期较短相关(P=0.026)。这项研究表明,肿瘤中 EOC 干细胞数量的定量可以作为疾病预测指标,并可应用于早期卵巢癌的治疗选择。