Identification of a Novel Subpopulation of Tumor-Initiating Cells from Gemcitabine-Resistant Pancreatic Ductal Adenocarcinoma Patients

被引:10
|
作者
Shimizu, Kazuya [1 ,2 ]
Chiba, Sachie [2 ]
Hori, Yuichi [2 ]
机构
[1] Kobe Med Ctr, Dept Internal Med, Kobe, Hyogo, Japan
[2] Kobe Univ, Grad Sch Hlth Sci, Dept Biophys, Div Med Chem, Kobe, Hyogo 657, Japan
来源
PLOS ONE | 2013年 / 8卷 / 11期
关键词
CANCER STEM-CELLS; CD133; EXPRESSION; IN-VITRO; GROWTH; DIFFERENTIATION; METASTASIS; POPULATIONS; PHENOTYPE; CARCINOMA; THERAPY;
D O I
10.1371/journal.pone.0081283
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Pancreatic ductal adenocarcinoma is highly resistant to systemic chemotherapy. Although there are many reports using pancreatic cancer cells derived from patients who did not receive chemotherapy, characteristics of pancreatic cancer cells from chemotherapy-resistant patients remain unclear. In this study, we set out to establish a cancer cell line in disseminated cancer cells derived from gemcitabine-resistant pancreatic ductal adenocarcinoma patients. By use of in vitro co-culture system with stromal cells, we established a novel pancreatic tumor-initiating cell line. The cell line required its direct interaction with stromal cells for its in vitro clonogenic growth and passaging. Their direct interaction induced basal lamina-like extracellular matrix formation that maintained colony formation. The cell line expressed CD133 protein, which expression level changed autonomously and by culture conditions. These results demonstrated that there were novel pancreatic tumor-initiating cells that required direct interactions with stromal cells for their in vitro cultivation in gemcitabine-resistant pancreatic ductal adenocarcinoma. This cell line would help to develop novel therapies that enhance effects of gemcitabine or novel anti-cancer drugs.
引用
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页数:13
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