Identification and expansion of cancer stem cells in tumor tissues and peripheral blood derived from gastric adenocarcinoma patients

被引:0
作者
Tie Chen
Kun Yang
Jianhua Yu
Wentong Meng
Dandan Yuan
Feng Bi
Fang Liu
Jie Liu
Bing Dai
Xinzu Chen
Fang Wang
Fan Zeng
Hong Xu
Jiankun Hu
Xianming Mo
机构
[1] Laboratory of Stem Cell Biology,Department of Gastrointestinal Surgery
[2] State Key Laboratory of Biotherapy,undefined
[3] West China Hospital,undefined
[4] West China Medical School,undefined
[5] Sichuan University,undefined
[6] State Key Laboratory of Biotherapy,undefined
[7] West China Hospital,undefined
[8] West China Medical School,undefined
[9] Sichuan University,undefined
[10] Oncology,undefined
[11] State Key Laboratory of Biotherapy,undefined
[12] West China Hospital,undefined
[13] West China Medical School,undefined
[14] Sichuan University,undefined
来源
Cell Research | 2012年 / 22卷
关键词
cancer stem cells; gastric adenocarcinoma; CD44; CD54; circulating tumor cells;
D O I
暂无
中图分类号
学科分类号
摘要
Gastric cancer is the fourth most common cancer worldwide, with a high rate of death and low 5-year survival rate. To date, there is a lack of efficient therapeutic protocols for gastric cancer. Recent studies suggest that cancer stem cells (CSCs) are responsible for tumor initiation, invasion, metastasis, and resistance to anticancer therapies. Thus, therapies that target gastric CSCs are attractive. However, CSCs in human gastric adenocarcinoma (GAC) have not been described. Here, we identify CSCs in tumor tissues and peripheral blood from GAC patients. CSCs of human GAC (GCSCs) that are isolated from tumor tissues and peripheral blood of patients carried CD44 and CD54 surface markers, generated tumors that highly resemble the original human tumors when injected into immunodeficient mice, differentiated into gastric epithelial cells in vitro, and self-renewed in vivo and in vitro. Our findings suggest that effective therapeutic protocols must target GCSCs. The capture of GCSCs from the circulation of GAC patients also shows great potential for identification of a critical cell population potentially responsible for tumor metastasis, and provides an effective protocol for early diagnosis and longitudinal monitoring of gastric cancer.
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页码:248 / 258
页数:10
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