Department of Surgery, Experimental Surgery, Campus Charité Mitte, Campus Virchow Klinikum, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany.
Department of Hematology, Oncology and Tumor Immunology, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany.
Anticancer Res. 2020 Mar;40(3):1267-1275. doi: 10.21873/anticanres.14068.
BACKGROUND/AIM: Pancreatic ductal adenocarcinoma (PDAC) and extrahepatic cholangio-carcinoma (eCC) represent two cancer entities with devastating prognoses. Despite recent progress in research and treatment, therapy remains challenging. Cancer stem cells (CSCs) have been shown to play an important role in metastasis and chemoresistance. Therefore, CSCs may play a promising role as a potential therapeutic target.
A total of 31 patients (23 PDAC, 8 eCC) were included in the study. CSCs were analyzed in a single-cell suspension of tumor samples via fluorescence-activated cell scanning (FACS) with a functional Hoechst 33342 staining as well as a cell surface marker staining of the CSC-panel (CD24, CD44 and EpCAM) and markers to identify fibroblasts, leukocytes and components of the notch signaling pathway. Furthermore, the potential presence of CSCs among primary cancer-associated fibroblasts (CAFs) was assessed using the same FACS-panel.
We showed that CSCs are present in patient-derived dissociated tumor tissue. The functional and surface marker profile of CSC-detection did in fact correlate. The amount of CSCs was significantly correlated with tumor characteristics such as a higher UICC stadium and nodal invasion. CSCs were not restricted to the epithelial cell fraction in tumor tissues, which has been verified in independent analysis of primary cell cultures of CAFs.
Our study confirms the in vivo presence of CSCs in PDAC and eCC, stating a clinical significance thereof and thus their plausibility as therapeutic targets. In addition, stem-like cells also seem to constitute a part of the CAFs.
背景/目的:胰腺导管腺癌 (PDAC) 和肝外胆管癌 (eCC) 是两种预后极差的癌症实体。尽管在研究和治疗方面最近取得了进展,但治疗仍然具有挑战性。癌症干细胞 (CSC) 已被证明在转移和化疗耐药性中发挥重要作用。因此,CSC 可能作为一种有前途的治疗靶点发挥作用。
共纳入 31 名患者(23 名 PDAC,8 名 eCC)进行研究。通过荧光激活细胞扫描 (FACS) 用功能性 Hoechst 33342 染色以及 CSC 面板的细胞表面标志物染色(CD24、CD44 和 EpCAM)以及鉴定成纤维细胞、白细胞和 Notch 信号通路成分的标志物,在肿瘤样本的单细胞悬浮液中分析 CSCs。此外,还使用相同的 FACS 面板评估原发性癌相关成纤维细胞 (CAF) 中 CSC 的潜在存在。
我们表明 CSCs 存在于患者来源的分离肿瘤组织中。CSC 检测的功能和表面标志物特征确实相关。CSC 的数量与肿瘤特征显着相关,例如更高的 UICC 分期和淋巴结浸润。CSC 不仅局限于肿瘤组织中的上皮细胞部分,这在对 CAF 的原发性细胞培养的独立分析中得到了验证。
我们的研究证实了 PDAC 和 eCC 中 CSCs 的体内存在,说明了其临床意义,因此它们作为治疗靶点具有合理性。此外,类干细胞似乎也是 CAF 的一部分。